-
1
-
-
12244292196
-
Differentiation and definition of vascular-targeted therapies
-
Siemann, D. W.; Bibby, M. C.; Dark, G. G.; Dicker, A. P.; Eskens, F. A. L. M.; Horsman, M. R.; Marmé, D.; LoRusso, P. M. Differentiation and definition of vascular-targeted therapies Clin. Cancer Res. 2005, 11, 416-420
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 416-420
-
-
Siemann, D.W.1
Bibby, M.C.2
Dark, G.G.3
Dicker, A.P.4
Eskens, F.A.L.M.5
Horsman, M.R.6
Marmé, D.7
LoRusso, P.M.8
-
2
-
-
20344379950
-
Disrupting tumour blood vessels
-
Tozer, G. M.; Kanthou, C.; Baguley, B. C. Disrupting tumour blood vessels Nat. Rev. Cancer 2005, 5, 423-435 10.1038/nrc1628
-
(2005)
Nat. Rev. Cancer
, vol.5
, pp. 423-435
-
-
Tozer, G.M.1
Kanthou, C.2
Baguley, B.C.3
-
3
-
-
46749126105
-
Selective destruction of the tumour vasculature by targeting the endothelial cytoskeleton
-
Kanthou, C.; Tozer, G. M. Selective destruction of the tumour vasculature by targeting the endothelial cytoskeleton Drug Discovery Today: Ther. Strategies 2007, 4, 237-243 10.1016/j.ddstr.2008.03.003
-
(2007)
Drug Discovery Today: Ther. Strategies
, vol.4
, pp. 237-243
-
-
Kanthou, C.1
Tozer, G.M.2
-
4
-
-
80052933197
-
Basic and therapeutic aspects of angiogenesis
-
Potente, M.; Gerhardt, H.; Carmeliet, P. Basic and therapeutic aspects of angiogenesis Cell 2011, 146, 873-887 10.1016/j.cell.2011.08.039
-
(2011)
Cell
, vol.146
, pp. 873-887
-
-
Potente, M.1
Gerhardt, H.2
Carmeliet, P.3
-
5
-
-
30744479430
-
Angiogenesis in life, disease and medicine
-
Carmeliet, P. Angiogenesis in life, disease and medicine Nature 2005, 438, 932-936 10.1038/nature04478
-
(2005)
Nature
, vol.438
, pp. 932-936
-
-
Carmeliet, P.1
-
6
-
-
84885106382
-
Angiogenesis inhibitors in cancer therapy: Mechanistic perspective on classification and treatment rationales
-
El-Kenawi, A. E.; El-Remessy, A. B. Angiogenesis inhibitors in cancer therapy: mechanistic perspective on classification and treatment rationales Br. J. Pharmacol. 2013, 170, 712-729 10.1111/bph.12344
-
(2013)
Br. J. Pharmacol.
, vol.170
, pp. 712-729
-
-
El-Kenawi, A.E.1
El-Remessy, A.B.2
-
7
-
-
84903901969
-
Anti-angiogenic therapy for cancer: Current progress, unresolved questions and future directions
-
Vasudev, N. S.; Reynolds, A. R. Anti-angiogenic therapy for cancer: current progress, unresolved questions and future directions Angiogenesis 2014, 17, 471-494 10.1007/s10456-014-9420-y
-
(2014)
Angiogenesis
, vol.17
, pp. 471-494
-
-
Vasudev, N.S.1
Reynolds, A.R.2
-
8
-
-
78649833819
-
The unique characteristics of tumor vasculature and preclinical evidence for its selective disruption by tumor-vascular disrupting agents
-
Siemann, D. W. The unique characteristics of tumor vasculature and preclinical evidence for its selective disruption by tumor-vascular disrupting agents Cancer Treat. Rev. 2011, 37, 63-74 10.1016/j.ctrv.2010.05.001
-
(2011)
Cancer Treat. Rev.
, vol.37
, pp. 63-74
-
-
Siemann, D.W.1
-
9
-
-
84938420626
-
Modulation of the tumor vasculature and oxygenation to improve therapy
-
Siemann, D. W.; Horsman, M. R. Modulation of the tumor vasculature and oxygenation to improve therapy Pharmacol. Ther. 2015, 153, 107-124 10.1016/j.pharmthera.2015.06.006
-
(2015)
Pharmacol. Ther.
, vol.153
, pp. 107-124
-
-
Siemann, D.W.1
Horsman, M.R.2
-
10
-
-
65549164757
-
Microtubule depolymerizing vascular disrupting agents: Novel therapeutic agents for oncology and other pathologies
-
Kanthou, C.; Tozer, G. M. Microtubule depolymerizing vascular disrupting agents: novel therapeutic agents for oncology and other pathologies Int. J. Exp. Pathol. 2009, 90, 284-294 10.1111/j.1365-2613.2009.00651.x
-
(2009)
Int. J. Exp. Pathol.
, vol.90
, pp. 284-294
-
-
Kanthou, C.1
Tozer, G.M.2
-
11
-
-
0842311621
-
Vascular targeting agents as cancer therapeutics
-
Thorpe, P. E. Vascular targeting agents as cancer therapeutics Clin. Cancer Res. 2004, 10, 415-427 10.1158/1078-0432.CCR-0642-03
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 415-427
-
-
Thorpe, P.E.1
-
12
-
-
19344378137
-
Vascular disrupting agents: A new class of drug in cancer therapy
-
Gaya, A. M.; Rustin, G. J. S. Vascular disrupting agents: a new class of drug in cancer therapy Clin. Oncol. 2005, 17, 277-290 10.1016/j.clon.2004.11.011
-
(2005)
Clin. Oncol.
, vol.17
, pp. 277-290
-
-
Gaya, A.M.1
Rustin, G.J.S.2
-
13
-
-
80051638135
-
Randomized phase III placebo-controlled trial of carboplatin and paclitaxel with or without the vascular disrupting agent vadimezan (ASA404) in advanced non-small-cell lung cancer
-
Lara, P. N.; Douillard, J. Y.; Nakagawa, K.; von Pawel, J. v.; McKeage, M. J.; Albert, I.; Losonczy, G.; Reck, M.; Heo, D.-S.; Fan, X.; Fandi, A.; Scagliotti, G. Randomized phase III placebo-controlled trial of carboplatin and paclitaxel with or without the vascular disrupting agent vadimezan (ASA404) in advanced non-small-cell lung cancer J. Clin. Oncol. 2011, 29, 2965-2971 10.1200/JCO.2011.35.0660
-
(2011)
J. Clin. Oncol.
, vol.29
, pp. 2965-2971
-
-
Lara, P.N.1
Douillard, J.Y.2
Nakagawa, K.3
Pawel, V.J.V.4
McKeage, M.J.5
Albert, I.6
Losonczy, G.7
Reck, M.8
Heo, D.-S.9
Fan, X.10
Fandi, A.11
Scagliotti, G.12
-
14
-
-
80051612685
-
Clinical development of vascular disrupting agents: What lessons can we learn from ASA404?
-
LoRusso, P. M.; Boerner, S. A.; Hunsberger, S. Clinical development of vascular disrupting agents: what lessons can we learn from ASA404? J. Clin. Oncol. 2011, 29, 2952-2955 10.1200/JCO.2011.36.1311
-
(2011)
J. Clin. Oncol.
, vol.29
, pp. 2952-2955
-
-
LoRusso, P.M.1
Boerner, S.A.2
Hunsberger, S.3
-
15
-
-
84896705592
-
Plant-derived vascular disrupting agents: Compounds, actions, and clinical trials
-
Kretzschmann, V.; Fürst, R. Plant-derived vascular disrupting agents: compounds, actions, and clinical trials Phytochem. Rev. 2014, 13, 191-206 10.1007/s11101-013-9304-6
-
(2014)
Phytochem. Rev.
, vol.13
, pp. 191-206
-
-
Kretzschmann, V.1
Fürst, R.2
-
16
-
-
64049097460
-
Microtubule dynamics as a target in oncology
-
Risinger, A. L.; Giles, F. J.; Mooberry, S. L. Microtubule dynamics as a target in oncology Cancer Treat. Rev. 2009, 35, 255-261 10.1016/j.ctrv.2008.11.001
-
(2009)
Cancer Treat. Rev.
, vol.35
, pp. 255-261
-
-
Risinger, A.L.1
Giles, F.J.2
Mooberry, S.L.3
-
17
-
-
0014321783
-
Properties of the protein subunit of central-pair and outer-doublet microtubules of sea urchin flagella
-
Shelanski, M. L.; Taylor, E. W. Properties of the protein subunit of central-pair and outer-doublet microtubules of sea urchin flagella J. Cell Biol. 1968, 38, 304-315 10.1083/jcb.38.2.304
-
(1968)
J. Cell Biol.
, vol.38
, pp. 304-315
-
-
Shelanski, M.L.1
Taylor, E.W.2
-
18
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
Ravelli, R. B. G.; Gigant, B.; Curmi, P. A.; Jourdain, I.; Lachkar, S.; Sobel, A.; Knossow, M. Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain Nature 2004, 428, 198-202 10.1038/nature02393
-
(2004)
Nature
, vol.428
, pp. 198-202
-
-
Ravelli, R.B.G.1
Gigant, B.2
Curmi, P.A.3
Jourdain, I.4
Lachkar, S.5
Sobel, A.6
Knossow, M.7
-
19
-
-
37249020371
-
Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin
-
Bhattacharyya, B.; Panda, D.; Gupta, S.; Banerjee, M. Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin Med. Res. Rev. 2008, 28, 155-183 10.1002/med.20097
-
(2008)
Med. Res. Rev.
, vol.28
, pp. 155-183
-
-
Bhattacharyya, B.1
Panda, D.2
Gupta, S.3
Banerjee, M.4
-
20
-
-
84955730816
-
Colchicine-Update on mechanisms of action and therapeutic uses
-
Leung, Y. Y.; Hui, L. L. Y.; Kraus, V. B. Colchicine-Update on mechanisms of action and therapeutic uses Semin. Arthritis Rheum. 2015, 45, 341-350 10.1016/j.semarthrit.2015.06.013
-
(2015)
Semin. Arthritis Rheum.
, vol.45
, pp. 341-350
-
-
Leung, Y.Y.1
Hui, L.L.Y.2
Kraus, V.B.3
-
21
-
-
0023217561
-
Antineoplastic agents 122. Constituents of Combretum caffrum
-
Pettit, G. R.; Cragg, G. M.; Singh, S. B. Antineoplastic agents 122. Constituents of Combretum caffrum J. Nat. Prod. 1987, 50, 386-391 10.1021/np50051a008
-
(1987)
J. Nat. Prod.
, vol.50
, pp. 386-391
-
-
Pettit, G.R.1
Cragg, G.M.2
Singh, S.B.3
-
22
-
-
0029044610
-
Antineoplastic agents 322. Synthesis of combretastatin A-4 prodrugs
-
Pettit, G. R.; Temple, C. J.; Narayanan, V. L.; Varma, R.; Simpson, M. J.; Boyd, M. R.; Rener, G. A.; Bansal, N. Antineoplastic agents 322. Synthesis of combretastatin A-4 prodrugs Anti-Cancer Drug Des. 1995, 10, 299-309
-
(1995)
Anti-Cancer Drug Des.
, vol.10
, pp. 299-309
-
-
Pettit, G.R.1
Temple, C.J.2
Narayanan, V.L.3
Varma, R.4
Simpson, M.J.5
Boyd, M.R.6
Rener, G.A.7
Bansal, N.8
-
23
-
-
0024427745
-
Antimitotic natural products combretastatin A-4 and combretastatin A-2: Studies on the mechanism of their inhibition of the binding of colchicine to tubulin
-
Lin, C. M.; Ho, H. H.; Pettit, G. R.; Hamel, E. Antimitotic natural products combretastatin A-4 and combretastatin A-2: Studies on the mechanism of their inhibition of the binding of colchicine to tubulin Biochemistry 1989, 28, 6984-6991 10.1021/bi00443a031
-
(1989)
Biochemistry
, vol.28
, pp. 6984-6991
-
-
Lin, C.M.1
Ho, H.H.2
Pettit, G.R.3
Hamel, E.4
-
24
-
-
0030951899
-
Combretastatin A-4, an agent that displays potent and selective toxicity toward tumor vasculature
-
Dark, G. G.; Hill, S. A.; Prise, V. E.; Tozer, G. M.; Pettit, G. R.; Chaplin, D. J. Combretastatin A-4, an agent that displays potent and selective toxicity toward tumor vasculature Cancer Res. 1997, 57, 1829-1834
-
(1997)
Cancer Res.
, vol.57
, pp. 1829-1834
-
-
Dark, G.G.1
Hill, S.A.2
Prise, V.E.3
Tozer, G.M.4
Pettit, G.R.5
Chaplin, D.J.6
-
25
-
-
84946712566
-
Combretastatins: More than just vascular targeting agents?
-
Greene, L. M.; Meegan, M. J.; Zisterer, D. M. Combretastatins: more than just vascular targeting agents? J. Pharmacol. Exp. Ther. 2015, 355, 212-227 10.1124/jpet.115.226225
-
(2015)
J. Pharmacol. Exp. Ther.
, vol.355
, pp. 212-227
-
-
Greene, L.M.1
Meegan, M.J.2
Zisterer, D.M.3
-
26
-
-
84873680173
-
Vascular-disrupting agents in oncology
-
Mita, M. M.; Sargsyan, L.; Mita, A. C.; Spear, M. Vascular-disrupting agents in oncology Expert Opin. Invest. Drugs 2013, 22, 317-328 10.1517/13543784.2013.759557
-
(2013)
Expert Opin. Invest. Drugs
, vol.22
, pp. 317-328
-
-
Mita, M.M.1
Sargsyan, L.2
Mita, A.C.3
Spear, M.4
-
27
-
-
84908563532
-
Recent advances in vascular disrupting agents in cancer therapy
-
Porcu, E.; Bortolozzi, R.; Basso, G.; Viola, G. Recent advances in vascular disrupting agents in cancer therapy Future Med. Chem. 2014, 6, 1485-1498 10.4155/fmc.14.104
-
(2014)
Future Med. Chem.
, vol.6
, pp. 1485-1498
-
-
Porcu, E.1
Bortolozzi, R.2
Basso, G.3
Viola, G.4
-
28
-
-
84924956325
-
Tubulin colchicine binding site inhibitors as vascular disrupting agents in clinical developments
-
Ji, Y. T.; Liu, Y. N.; Liu, Z. P. Tubulin colchicine binding site inhibitors as vascular disrupting agents in clinical developments Curr. Med. Chem. 2015, 22, 1348-1360 10.2174/0929867322666150114163732
-
(2015)
Curr. Med. Chem.
, vol.22
, pp. 1348-1360
-
-
Ji, Y.T.1
Liu, Y.N.2
Liu, Z.P.3
-
29
-
-
84894612306
-
Deciphering the molecular mechanisms of anti-tubulin plant derived drugs
-
Barbier, P.; Tsvetkov, P. O.; Breuzard, G.; Devred, F. Deciphering the molecular mechanisms of anti-tubulin plant derived drugs Phytochem. Rev. 2014, 13, 157-169 10.1007/s11101-013-9302-8
-
(2014)
Phytochem. Rev.
, vol.13
, pp. 157-169
-
-
Barbier, P.1
Tsvetkov, P.O.2
Breuzard, G.3
Devred, F.4
-
30
-
-
84883012772
-
Microtubule-associated proteins and tubulin interaction by isothermal titration calorimetry
-
John, J. C. Leslie, W. Academic Press: New York
-
Tsvetkov, P. O.; Barbier, P.; Breuzard, G.; Peyrot, V.; Devred, F. Microtubule-associated proteins and tubulin interaction by isothermal titration calorimetry. In Methods in Cell Biology; John, J. C.; Leslie, W., Eds.; Academic Press: New York, 2013; Vol. 115, pp 283-302.
-
(2013)
Methods in Cell Biology
, vol.115
, pp. 283-302
-
-
Tsvetkov, P.O.1
Barbier, P.2
Breuzard, G.3
Peyrot, V.4
Devred, F.5
-
31
-
-
78649874504
-
Quick and simple detection technique to assess the binding of antimicrotubule agents to the colchicine-binding site
-
Fortin, S.; Lacroix, J.; Côté, M. F.; Moreau, E.; Petitclerc, é.; C.-Gaudreault, R. Quick and simple detection technique to assess the binding of antimicrotubule agents to the colchicine-binding site Biol. Proced. Online 2010, 12, 113-117 10.1007/s12575-010-9029-5
-
(2010)
Biol. Proced. Online
, vol.12
, pp. 113-117
-
-
Fortin, S.1
Lacroix, J.2
Côté, M.F.3
Moreau, E.4
Petitclerc, É.5
Gaudreault, C.R.6
-
32
-
-
84901289480
-
Novel colchicine-site binders with a cyclohexanedione scaffold identified through a ligand-based virtual screening approach
-
Canela, M. D.; Pérez-Pérez, M. J.; Noppen, S.; Sáez-Calvo, G.; Díaz, J. F.; Camarasa, M. J.; Liekens, S.; Priego, E. M. Novel colchicine-site binders with a cyclohexanedione scaffold identified through a ligand-based virtual screening approach J. Med. Chem. 2014, 57, 3924-3938 10.1021/jm401939g
-
(2014)
J. Med. Chem.
, vol.57
, pp. 3924-3938
-
-
Canela, M.D.1
Pérez-Pérez, M.J.2
Noppen, S.3
Sáez-Calvo, G.4
Díaz, J.F.5
Camarasa, M.J.6
Liekens, S.7
Priego, E.M.8
-
33
-
-
84958984585
-
Targeting the colchicine site in tubulin through cyclohexanedione derivatives
-
Canela, M. D.; Bueno, O.; Noppen, S.; Sáez Calvo, G.; Estévez Gallego, J.; Díaz, J. F.; Camarasa, M. J.; Liekens, S.; Pérez-Pérez, M. J.; Priego, E. M. Targeting the colchicine site in tubulin through cyclohexanedione derivatives RSC Adv. 2016, 6, 19492-19506 10.1039/C5RA26807A
-
(2016)
RSC Adv.
, vol.6
, pp. 19492-19506
-
-
Canela, M.D.1
Bueno, O.2
Noppen, S.3
Sáez Calvo, G.4
Estévez Gallego, J.5
Díaz, J.F.6
Camarasa, M.J.7
Liekens, S.8
Pérez-Pérez, M.J.9
Priego, E.M.10
-
34
-
-
84885030356
-
Synthesis of a 2-aryl-3-aroyl indole salt (OXi8007) resembling Combretastatin A-4 with application as a vascular disrupting agent
-
Hadimani, M. B.; MacDonough, M. T.; Ghatak, A.; Strecker, T. E.; Lopez, R.; Sriram, M.; Nguyen, B. L.; Hall, J. J.; Kessler, R. J.; Shirali, A. R.; Liu, L.; Garner, C. M.; Pettit, G. R.; Hamel, E.; Chaplin, D. J.; Mason, R. P.; Trawick, M. L.; Pinney, K. G. Synthesis of a 2-aryl-3-aroyl indole salt (OXi8007) resembling Combretastatin A-4 with application as a vascular disrupting agent J. Nat. Prod. 2013, 76, 1668-1678 10.1021/np400374w
-
(2013)
J. Nat. Prod.
, vol.76
, pp. 1668-1678
-
-
Hadimani, M.B.1
MacDonough, M.T.2
Ghatak, A.3
Strecker, T.E.4
Lopez, R.5
Sriram, M.6
Nguyen, B.L.7
Hall, J.J.8
Kessler, R.J.9
Shirali, A.R.10
Liu, L.11
Garner, C.M.12
Pettit, G.R.13
Hamel, E.14
Chaplin, D.J.15
Mason, R.P.16
Trawick, M.L.17
Pinney, K.G.18
-
35
-
-
33744820579
-
Medicinal chemistry of combretastatin A4: Present and future directions
-
Tron, G. C.; Pirali, T.; Sorba, G.; Pagliai, F.; Busacca, S.; Genazzani, A. A. Medicinal chemistry of combretastatin A4: present and future directions J. Med. Chem. 2006, 49, 3033-3044 10.1021/jm0512903
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3033-3044
-
-
Tron, G.C.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
36
-
-
84867889521
-
An overview of tubulin inhibitors that interact with the colchicine binding site
-
Lu, Y.; Chen, J.; Xiao, M.; Li, W.; Miller, D. D. An overview of tubulin inhibitors that interact with the colchicine binding site Pharm. Res. 2012, 29, 2943-2971 10.1007/s11095-012-0828-z
-
(2012)
Pharm. Res.
, vol.29
, pp. 2943-2971
-
-
Lu, Y.1
Chen, J.2
Xiao, M.3
Li, W.4
Miller, D.D.5
-
37
-
-
79851496869
-
Developments of combretastatin A-4 derivatives as anticancer agents
-
Shan, Y. S.; Zhang, J.; Liu, Z.; Wang, M.; Dong, Y. Developments of combretastatin A-4 derivatives as anticancer agents Curr. Med. Chem. 2011, 18, 523-538 10.2174/092986711794480221
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 523-538
-
-
Shan, Y.S.1
Zhang, J.2
Liu, Z.3
Wang, M.4
Dong, Y.5
-
38
-
-
79960006369
-
Biological potential and structure-activity relationships of most recently developed vascular disrupting agents: An overview of new derivatives of natural combretastatin A-4
-
Marrelli, M.; Conforti, F.; Statti, G. A.; Cachet, X.; Michel, S.; Tillequin, F.; Menichini, F. Biological potential and structure-activity relationships of most recently developed vascular disrupting agents: An overview of new derivatives of natural combretastatin A-4 Curr. Med. Chem. 2011, 18, 3035-3081 10.2174/092986711796391642
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 3035-3081
-
-
Marrelli, M.1
Conforti, F.2
Statti, G.A.3
Cachet, X.4
Michel, S.5
Tillequin, F.6
Menichini, F.7
-
39
-
-
84940909354
-
Recent advancement in discovery and development of natural product combretastatin-inspired anticancer agents
-
Patil, P. O.; Patil, A. G.; Rane, R. A.; Patil, P. C.; Deshmukh, P. K.; Bari, S. B.; Patil, D. A.; Naphade, S. S. Recent advancement in discovery and development of natural product combretastatin-inspired anticancer agents Anti-Cancer Agents Med. Chem. 2015, 15, 955-969 10.2174/1871520615666150526141259
-
(2015)
Anti-Cancer Agents Med. Chem.
, vol.15
, pp. 955-969
-
-
Patil, P.O.1
Patil, A.G.2
Rane, R.A.3
Patil, P.C.4
Deshmukh, P.K.5
Bari, S.B.6
Patil, D.A.7
Naphade, S.S.8
-
40
-
-
84876727508
-
Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers
-
Rajak, H.; Kumar Dewangan, P.; Patel, V.; Kumar Jain, D.; Singh, A.; Veerasamy, R.; Chander Sharma, P.; Dixit, A. Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers Curr. Pharm. Des. 2013, 19, 1923-1955 10.2174/1381612811319100013
-
(2013)
Curr. Pharm. Des.
, vol.19
, pp. 1923-1955
-
-
Rajak, H.1
Kumar Dewangan, P.2
Patel, V.3
Kumar Jain, D.4
Singh, A.5
Veerasamy, R.6
Chander Sharma, P.7
Dixit, A.8
-
41
-
-
84907535079
-
Recent developments in tubulin polymerization inhibitors: An overview
-
Kaur, R.; Kaur, G.; Gill, R. K.; Soni, R.; Bariwal, J. Recent developments in tubulin polymerization inhibitors: An overview Eur. J. Med. Chem. 2014, 87, 89-124 10.1016/j.ejmech.2014.09.051
-
(2014)
Eur. J. Med. Chem.
, vol.87
, pp. 89-124
-
-
Kaur, R.1
Kaur, G.2
Gill, R.K.3
Soni, R.4
Bariwal, J.5
-
42
-
-
84920580115
-
New ligands of the tubulin colchicine site based on X-ray structures
-
álvarez, R.; Medarde, M.; Peláez, R. New ligands of the tubulin colchicine site based on X-ray structures Curr. Top. Med. Chem. 2014, 14, 2231-2252 10.2174/1568026614666141130092637
-
(2014)
Curr. Top. Med. Chem.
, vol.14
, pp. 2231-2252
-
-
Álvarez, R.1
Medarde, M.2
Peláez, R.3
-
43
-
-
84555195099
-
The tubulin colchicine domain: A molecular modeling perspective
-
Massarotti, A.; Coluccia, A.; Silvestri, R.; Sorba, G.; Brancale, A. The tubulin colchicine domain: a molecular modeling perspective ChemMedChem 2012, 7, 33-42 10.1002/cmdc.201100361
-
(2012)
ChemMedChem
, vol.7
, pp. 33-42
-
-
Massarotti, A.1
Coluccia, A.2
Silvestri, R.3
Sorba, G.4
Brancale, A.5
-
44
-
-
84863401577
-
Polygamain, a new microtubule depolymerizing agent that occupies a unique pharmacophore in the colchicine site
-
Hartley, R. M.; Peng, J.; Fest, G. A.; Dakshanamurthy, S.; Frantz, D. E.; Brown, M. L.; Mooberry, S. L. Polygamain, a new microtubule depolymerizing agent that occupies a unique pharmacophore in the colchicine site Mol. Pharmacol. 2012, 81, 431-439 10.1124/mol.111.075838
-
(2012)
Mol. Pharmacol.
, vol.81
, pp. 431-439
-
-
Hartley, R.M.1
Peng, J.2
Fest, G.A.3
Dakshanamurthy, S.4
Frantz, D.E.5
Brown, M.L.6
Mooberry, S.L.7
-
45
-
-
1942438028
-
Microtubules as target for anticancer drugs
-
Jordan, M. A.; Wilson, L. Microtubules as target for anticancer drugs Nat. Rev. Cancer 2004, 4, 253-265 10.1038/nrc1317
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
46
-
-
0029066847
-
Antineoplastic agents. 291. Isolation and synthesis of combretastatins A-4, A-5, and A-6
-
Pettit, G. R.; Singh, S. B.; Boyd, M. R.; Hamel, E.; Pettit, R. K.; Schmidt, J. M.; Hogan, F. Antineoplastic agents. 291. Isolation and synthesis of combretastatins A-4, A-5, and A-6 J. Med. Chem. 1995, 38, 1666-1672 10.1021/jm00010a011
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1666-1672
-
-
Pettit, G.R.1
Singh, S.B.2
Boyd, M.R.3
Hamel, E.4
Pettit, R.K.5
Schmidt, J.M.6
Hogan, F.7
-
47
-
-
0032410472
-
Antineoplastic agents 393. Synthesis of the trans-isomer of combretastatin A-4 prodrug
-
Pettit, G. R.; Rhodes, M. R.; Herald, D. L.; Chaplin, D. J.; Stratford, M. R. L.; Hamel, E.; Pettit, R. K.; Chapuis, J. C.; Oliva, D. Antineoplastic agents 393. Synthesis of the trans-isomer of combretastatin A-4 prodrug Anti-Cancer Drug Des. 1998, 13, 981-993
-
(1998)
Anti-Cancer Drug Des.
, vol.13
, pp. 981-993
-
-
Pettit, G.R.1
Rhodes, M.R.2
Herald, D.L.3
Chaplin, D.J.4
Stratford, M.R.L.5
Hamel, E.6
Pettit, R.K.7
Chapuis, J.C.8
Oliva, D.9
-
48
-
-
0033814533
-
Antineoplastic agents 429. Syntheses of the combretastatin A-1 and combretastatin B-1 prodrugs
-
Pettit, G. R.; Lippert, J. W. Antineoplastic agents 429. Syntheses of the combretastatin A-1 and combretastatin B-1 prodrugs Anti-Cancer Drug Des. 2000, 15, 203-216
-
(2000)
Anti-Cancer Drug Des.
, vol.15
, pp. 203-216
-
-
Pettit, G.R.1
Lippert, J.W.2
-
49
-
-
15144356733
-
Novel combretastatin analogues effective against murine solid tumors: Design and structure-activity relationships
-
Ohsumi, K.; Nakagawa, R.; Fukuda, Y.; Hatanaka, T.; Morinaga, Y.; Nihei, Y.; Ohishi, K.; Suga, Y.; Akiyama, Y.; Tsuji, T. Novel combretastatin analogues effective against murine solid tumors: Design and structure-activity relationships J. Med. Chem. 1998, 41, 3022-3032 10.1021/jm980101w
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3022-3032
-
-
Ohsumi, K.1
Nakagawa, R.2
Fukuda, Y.3
Hatanaka, T.4
Morinaga, Y.5
Nihei, Y.6
Ohishi, K.7
Suga, Y.8
Akiyama, Y.9
Tsuji, T.10
-
50
-
-
38149097967
-
Oxidative metabolism of combretastatin A-1 produces quinone intermediates with the potential to bind to nucleophiles and to enhance oxidative stress via free radicals
-
Folkes, L. K.; Christlieb, M.; Madej, E.; Stratford, M. R. L.; Wardman, P. Oxidative metabolism of combretastatin A-1 produces quinone intermediates with the potential to bind to nucleophiles and to enhance oxidative stress via free radicals Chem. Res. Toxicol. 2007, 20, 1885-1894 10.1021/tx7002195
-
(2007)
Chem. Res. Toxicol.
, vol.20
, pp. 1885-1894
-
-
Folkes, L.K.1
Christlieb, M.2
Madej, E.3
Stratford, M.R.L.4
Wardman, P.5
-
51
-
-
0032542045
-
Syntheses and antitumor activity of cis-restricted combretastatins: 5-Membered heterocyclic analogues
-
Ohsumi, K.; Hatanaka, T.; Fujita, K.; Nakagawa, R.; Fukuda, Y.; Nihei, Y.; Suga, Y.; Morinaga, Y.; Akiyama, Y.; Tsuji, T. Syntheses and antitumor activity of cis-restricted combretastatins: 5-Membered heterocyclic analogues Bioorg. Med. Chem. Lett. 1998, 8, 3153-3158 10.1016/S0960-894X(98)00579-4
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 3153-3158
-
-
Ohsumi, K.1
Hatanaka, T.2
Fujita, K.3
Nakagawa, R.4
Fukuda, Y.5
Nihei, Y.6
Suga, Y.7
Morinaga, Y.8
Akiyama, Y.9
Tsuji, T.10
-
52
-
-
79960639980
-
Convergent synthesis and biological evaluation of 2-amino-4-(3′,4′,5′-trimethoxyphenyl)-5-aryl thiazoles as microtubule targeting agents
-
Romagnoli, R.; Baraldi, P. G.; Brancale, A.; Ricci, A.; Hamel, E.; Bortolozzi, R.; Basso, G.; Viola, G. Convergent synthesis and biological evaluation of 2-amino-4-(3′,4′,5′-trimethoxyphenyl)-5-aryl thiazoles as microtubule targeting agents J. Med. Chem. 2011, 54, 5144-5153 10.1021/jm200392p
-
(2011)
J. Med. Chem.
, vol.54
, pp. 5144-5153
-
-
Romagnoli, R.1
Baraldi, P.G.2
Brancale, A.3
Ricci, A.4
Hamel, E.5
Bortolozzi, R.6
Basso, G.7
Viola, G.8
-
53
-
-
0037061622
-
Potent, orally active heterocycle-based combretastatin A-4 analogues: Synthesis, structure-activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation
-
Wang, L.; Woods, K. W.; Li, Q.; Barr, K. J.; McCroskey, R. W.; Hannick, S. M.; Gherke, L.; Credo, R. B.; Hui, Y.-H.; Marsh, K.; Warner, R.; Lee, J. Y.; Zielinski-Mozng, N.; Frost, D.; Rosenberg, S. H.; Sham, H. L. Potent, orally active heterocycle-based combretastatin A-4 analogues: synthesis, structure-activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation J. Med. Chem. 2002, 45, 1697-1711 10.1021/jm010523x
-
(2002)
J. Med. Chem.
, vol.45
, pp. 1697-1711
-
-
Wang, L.1
Woods, K.W.2
Li, Q.3
Barr, K.J.4
McCroskey, R.W.5
Hannick, S.M.6
Gherke, L.7
Credo, R.B.8
Hui, Y.-H.9
Marsh, K.10
Warner, R.11
Lee, J.Y.12
Zielinski-Mozng, N.13
Frost, D.14
Rosenberg, S.H.15
Sham, H.L.16
-
54
-
-
33847399088
-
Highly potent triazole-based tubulin polymerization inhibitors
-
Zhang, Q.; Peng, Y.; Wang, X. I.; Keenan, S. M.; Arora, S.; Welsh, W. J. Highly potent triazole-based tubulin polymerization inhibitors J. Med. Chem. 2007, 50, 749-754 10.1021/jm061142s
-
(2007)
J. Med. Chem.
, vol.50
, pp. 749-754
-
-
Zhang, Q.1
Peng, Y.2
Wang, X.I.3
Keenan, S.M.4
Arora, S.5
Welsh, W.J.6
-
55
-
-
62449302405
-
Novel microtubule polymerization inhibitor with potent antiproliferative and antitumor activity
-
Arora, S.; Wang, X. I.; Keenan, S. M.; Andaya, C.; Zhang, Q.; Peng, Y.; Welsh, W. J. Novel microtubule polymerization inhibitor with potent antiproliferative and antitumor activity Cancer Res. 2009, 69, 1910-1915 10.1158/0008-5472.CAN-08-0877
-
(2009)
Cancer Res.
, vol.69
, pp. 1910-1915
-
-
Arora, S.1
Wang, X.I.2
Keenan, S.M.3
Andaya, C.4
Zhang, Q.5
Peng, Y.6
Welsh, W.J.7
-
56
-
-
1842741030
-
Examination of the 1,4-disubstituted azetidinone ring system as a template for combretastatin A-4 conformationally restricted analogue design
-
Sun, L.; Vasilevich, N. I.; Fuselier, J. A.; Hocart, S. J.; Coy, D. H. Examination of the 1,4-disubstituted azetidinone ring system as a template for combretastatin A-4 conformationally restricted analogue design Bioorg. Med. Chem. Lett. 2004, 14, 2041-2046 10.1016/j.bmcl.2004.02.050
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 2041-2046
-
-
Sun, L.1
Vasilevich, N.I.2
Fuselier, J.A.3
Hocart, S.J.4
Coy, D.H.5
-
57
-
-
78650312289
-
Synthesis and evaluation of azetidinone analogues of combretastatin A-4 as tubulin targeting agents
-
O'Boyle, N. M.; Carr, M.; Greene, L. M.; Bergin, O.; Nathwani, S. M.; McCabe, T.; Lloyd, D. G.; Zisterer, D. M.; Meegan, M. J. Synthesis and evaluation of azetidinone analogues of combretastatin A-4 as tubulin targeting agents J. Med. Chem. 2010, 53, 8569-8584 10.1021/jm101115u
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8569-8584
-
-
O'Boyle, N.M.1
Carr, M.2
Greene, L.M.3
Bergin, O.4
Nathwani, S.M.5
McCabe, T.6
Lloyd, D.G.7
Zisterer, D.M.8
Meegan, M.J.9
-
58
-
-
84955250153
-
Synthesis and biochemical evaluation of 3-phenoxy-1,4-diarylazetidin-2-ones as tubulin-targeting antitumor agents
-
Greene, T. F.; Wang, S.; Greene, L. M.; Nathwani, S. M.; Pollock, J. K.; Malebari, A. M.; McCabe, T.; Twamley, B.; O'Boyle, N. M.; Zisterer, D. M.; Meegan, M. J. Synthesis and biochemical evaluation of 3-phenoxy-1,4-diarylazetidin-2-ones as tubulin-targeting antitumor agents J. Med. Chem. 2016, 59, 90-113 10.1021/acs.jmedchem.5b01086
-
(2016)
J. Med. Chem.
, vol.59
, pp. 90-113
-
-
Greene, T.F.1
Wang, S.2
Greene, L.M.3
Nathwani, S.M.4
Pollock, J.K.5
Malebari, A.M.6
McCabe, T.7
Twamley, B.8
O'Boyle, N.M.9
Zisterer, D.M.10
Meegan, M.J.11
-
59
-
-
84924666726
-
Quantum chemistry calculation-aided structural optimization of combretastatin A-4-like tubulin polymerization inhibitors: Improved stability and biological activity
-
Jiang, J.; Zheng, C.; Zhu, K.; Liu, J.; Sun, N.; Wang, C.; Jiang, H.; Zhu, J.; Luo, C.; Zhou, Y. Quantum chemistry calculation-aided structural optimization of combretastatin A-4-like tubulin polymerization inhibitors: improved stability and biological activity J. Med. Chem. 2015, 58, 2538-2546 10.1021/acs.jmedchem.5b00118
-
(2015)
J. Med. Chem.
, vol.58
, pp. 2538-2546
-
-
Jiang, J.1
Zheng, C.2
Zhu, K.3
Liu, J.4
Sun, N.5
Wang, C.6
Jiang, H.7
Zhu, J.8
Luo, C.9
Zhou, Y.10
-
60
-
-
0032492959
-
Antineoplastic agents. 379. Synthesis of phenstatin phosphate1a
-
Pettit, G. R.; Toki, B.; Herald, D. L.; Verdier-Pinard, P.; Boyd, M. R.; Hamel, E.; Pettit, R. K. Antineoplastic agents. 379. Synthesis of phenstatin phosphate1a J. Med. Chem. 1998, 41, 1688-1695 10.1021/jm970644q
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1688-1695
-
-
Pettit, G.R.1
Toki, B.2
Herald, D.L.3
Verdier-Pinard, P.4
Boyd, M.R.5
Hamel, E.6
Pettit, R.K.7
-
61
-
-
77956298509
-
Identification of CKD-516: A potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors
-
Lee, J.; Kim, S. J.; Choi, H.; Kim, Y. H.; Lim, I. T.; Yang, H.-m.; Lee, C. S.; Kang, H. R.; Ahn, S. K.; Moon, S. K.; Kim, D.-H.; Lee, S.; Choi, N. S.; Lee, K. J. Identification of CKD-516: a potent tubulin polymerization inhibitor with marked antitumor activity against murine and human solid tumors J. Med. Chem. 2010, 53, 6337-6354 10.1021/jm1002414
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6337-6354
-
-
Lee, J.1
Kim, S.J.2
Choi, H.3
Kim, Y.H.4
Lim, I.T.5
Yang, H.-M.6
Lee, C.S.7
Kang, H.R.8
Ahn, S.K.9
Moon, S.K.10
Kim, D.-H.11
Lee, S.12
Choi, N.S.13
Lee, K.J.14
-
62
-
-
84957541113
-
Phase i study of CKD-516, a novel vascular disrupting agent, in patients with advanced solid tumors
-
Oh, D. Y.; Kim, T. M.; Han, S. W.; Shin, D. Y.; Lee, Y. G.; Lee, K. W.; Kim, J. H.; Kim, T. Y.; Jang, I. J.; Lee, J. S.; Bang, Y. J. Phase I study of CKD-516, a novel vascular disrupting agent, in patients with advanced solid tumors Cancer Res. Treat. 2016, 48, 28-36 10.4143/crt.2014.258
-
(2016)
Cancer Res. Treat.
, vol.48
, pp. 28-36
-
-
Oh, D.Y.1
Kim, T.M.2
Han, S.W.3
Shin, D.Y.4
Lee, Y.G.5
Lee, K.W.6
Kim, J.H.7
Kim, T.Y.8
Jang, I.J.9
Lee, J.S.10
Bang, Y.J.11
-
63
-
-
3042740981
-
BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo
-
Kuo, C. C.; Hsieh, H. P.; Pan, W. Y.; Chen, C. P.; Liou, J. P.; Lee, S. J.; Chang, Y. L.; Chen, L. T.; Chen, C. T.; Chang, J. Y. BPR0L075, a novel synthetic indole compound with antimitotic activity in human cancer cells, exerts effective antitumoral activity in vivo Cancer Res. 2004, 64, 4621-4628 10.1158/0008-5472.CAN-03-3474
-
(2004)
Cancer Res.
, vol.64
, pp. 4621-4628
-
-
Kuo, C.C.1
Hsieh, H.P.2
Pan, W.Y.3
Chen, C.P.4
Liou, J.P.5
Lee, S.J.6
Chang, Y.L.7
Chen, L.T.8
Chen, C.T.9
Chang, J.Y.10
-
64
-
-
79955424472
-
Scaffold-hopping strategy: Synthesis and biological evaluation of 5,6-fused bicyclic heteroaromatics to identify orally bioavailable anticancer agents
-
Tung, Y. S.; Coumar, M. S.; Wu, Y. S.; Shiao, H. Y.; Chang, J. Y.; Liou, J. P.; Shukla, P.; Chang, C. W.; Chang, C. Y.; Kuo, C. C.; Yeh, T. K.; Lin, C. Y.; Wu, J. S.; Wu, S. Y.; Liao, C. C.; Hsieh, H. P. Scaffold-hopping strategy: synthesis and biological evaluation of 5,6-fused bicyclic heteroaromatics to identify orally bioavailable anticancer agents J. Med. Chem. 2011, 54, 3076-3080 10.1021/jm101027s
-
(2011)
J. Med. Chem.
, vol.54
, pp. 3076-3080
-
-
Tung, Y.S.1
Coumar, M.S.2
Wu, Y.S.3
Shiao, H.Y.4
Chang, J.Y.5
Liou, J.P.6
Shukla, P.7
Chang, C.W.8
Chang, C.Y.9
Kuo, C.C.10
Yeh, T.K.11
Lin, C.Y.12
Wu, J.S.13
Wu, S.Y.14
Liao, C.C.15
Hsieh, H.P.16
-
65
-
-
80052351229
-
Discovery of 7-hydroxy-6-methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan (BNC105), a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties
-
Flynn, B. L.; Gill, G. S.; Grobelny, D. W.; Chaplin, J. H.; Paul, D.; Leske, A. F.; Lavranos, T. C.; Chalmers, D. K.; Charman, S. A.; Kostewicz, E.; Shackleford, D. M.; Morizzi, J.; Hamel, E.; Jung, M. K.; Kremmidiotis, G. Discovery of 7-hydroxy-6-methoxy-2-methyl-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan (BNC105), a tubulin polymerization inhibitor with potent antiproliferative and tumor vascular disrupting properties J. Med. Chem. 2011, 54, 6014-6027 10.1021/jm200454y
-
(2011)
J. Med. Chem.
, vol.54
, pp. 6014-6027
-
-
Flynn, B.L.1
Gill, G.S.2
Grobelny, D.W.3
Chaplin, J.H.4
Paul, D.5
Leske, A.F.6
Lavranos, T.C.7
Chalmers, D.K.8
Charman, S.A.9
Kostewicz, E.10
Shackleford, D.M.11
Morizzi, J.12
Hamel, E.13
Jung, M.K.14
Kremmidiotis, G.15
-
66
-
-
77953423945
-
BNC105: A novel tubulin polymerization inhibitor that selectively disrupts tumor vasculature and displays single-agent antitumor efficacy
-
Kremmidiotis, G.; Leske, A. F.; Lavranos, T. C.; Beaumont, D.; Gasic, J.; Hall, A.; O'Callaghan, M.; Matthews, C. A.; Flynn, B. BNC105: A novel tubulin polymerization inhibitor that selectively disrupts tumor vasculature and displays single-agent antitumor efficacy Mol. Cancer Ther. 2010, 9, 1562-1573 10.1158/1535-7163.MCT-09-0815
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 1562-1573
-
-
Kremmidiotis, G.1
Leske, A.F.2
Lavranos, T.C.3
Beaumont, D.4
Gasic, J.5
Hall, A.6
O'Callaghan, M.7
Matthews, C.A.8
Flynn, B.9
-
67
-
-
77949378899
-
5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors
-
Nien, C. Y.; Chen, Y. C.; Kuo, C. C.; Hsieh, H. P.; Chang, C. Y.; Wu, J. S.; Wu, S. Y.; Liou, J. P.; Chang, J. Y. 5-Amino-2-aroylquinolines as highly potent tubulin polymerization inhibitors J. Med. Chem. 2010, 53, 2309-2313 10.1021/jm900685y
-
(2010)
J. Med. Chem.
, vol.53
, pp. 2309-2313
-
-
Nien, C.Y.1
Chen, Y.C.2
Kuo, C.C.3
Hsieh, H.P.4
Chang, C.Y.5
Wu, J.S.6
Wu, S.Y.7
Liou, J.P.8
Chang, J.Y.9
-
68
-
-
84911364250
-
3-(3,4,5-Trimethoxyphenylselenyl)-1H-indoles and their selenoxides as combretastatin A-4 analogs: Microwave-assisted synthesis and biological evaluation
-
Wen, Z.; Xu, J.; Wang, Z.; Qi, H.; Xu, Q.; Bai, Z.; Zhang, Q.; Bao, K.; Wu, Y.; Zhang, W. 3-(3,4,5-Trimethoxyphenylselenyl)-1H-indoles and their selenoxides as combretastatin A-4 analogs: Microwave-assisted synthesis and biological evaluation Eur. J. Med. Chem. 2015, 90, 184-194 10.1016/j.ejmech.2014.11.024
-
(2015)
Eur. J. Med. Chem.
, vol.90
, pp. 184-194
-
-
Wen, Z.1
Xu, J.2
Wang, Z.3
Qi, H.4
Xu, Q.5
Bai, Z.6
Zhang, Q.7
Bao, K.8
Wu, Y.9
Zhang, W.10
-
69
-
-
84927647021
-
Design, synthesis, in vitro, and in vivo anticancer and antiangiogenic activity of novel 3-arylaminobenzofuran derivatives targeting the colchicine site on tubulin
-
Romagnoli, R.; Baraldi, P. G.; Salvador, M. K.; Prencipe, F.; Lopez-Cara, C.; Schiaffino Ortega, S.; Brancale, A.; Hamel, E.; Castagliuolo, I.; Mitola, S.; Ronca, R.; Bortolozzi, R.; Porcù, E.; Basso, G.; Viola, G. Design, synthesis, in vitro, and in vivo anticancer and antiangiogenic activity of novel 3-arylaminobenzofuran derivatives targeting the colchicine site on tubulin J. Med. Chem. 2015, 58, 3209-3222 10.1021/acs.jmedchem.5b00155
-
(2015)
J. Med. Chem.
, vol.58
, pp. 3209-3222
-
-
Romagnoli, R.1
Baraldi, P.G.2
Salvador, M.K.3
Prencipe, F.4
Lopez-Cara, C.5
Schiaffino Ortega, S.6
Brancale, A.7
Hamel, E.8
Castagliuolo, I.9
Mitola, S.10
Ronca, R.11
Bortolozzi, R.12
Porcù, E.13
Basso, G.14
Viola, G.15
-
70
-
-
84939138196
-
New indole tubulin assembly inhibitors cause stable arrest of mitotic progression, enhanced stimulation of natural killer cell cytotoxic activity, and repression of Hedgehog-dependent cancer
-
La Regina, G.; Bai, R.; Coluccia, A.; Famiglini, V.; Pelliccia, S.; Passacantilli, S.; Mazzoccoli, C.; Ruggieri, V.; Verrico, A.; Miele, A.; Monti, L.; Nalli, M.; Alfonsi, R.; Di Marcotullio, L.; Gulino, A.; Ricci, B.; Soriani, A.; Santoni, A.; Caraglia, M.; Porto, S.; Da Pozzo, E.; Martini, C.; Brancale, A.; Marinelli, L.; Novellino, E.; Vultaggio, S.; Varasi, M.; Mercurio, C.; Bigogno, C.; Dondio, G.; Hamel, E.; Lavia, P.; Silvestri, R. New indole tubulin assembly inhibitors cause stable arrest of mitotic progression, enhanced stimulation of natural killer cell cytotoxic activity, and repression of Hedgehog-dependent cancer J. Med. Chem. 2015, 58, 5789-5807 10.1021/acs.jmedchem.5b00310
-
(2015)
J. Med. Chem.
, vol.58
, pp. 5789-5807
-
-
La Regina, G.1
Bai, R.2
Coluccia, A.3
Famiglini, V.4
Pelliccia, S.5
Passacantilli, S.6
Mazzoccoli, C.7
Ruggieri, V.8
Verrico, A.9
Miele, A.10
Monti, L.11
Nalli, M.12
Alfonsi, R.13
Di Marcotullio, L.14
Gulino, A.15
Ricci, B.16
Soriani, A.17
Santoni, A.18
Caraglia, M.19
Porto, S.20
Da Pozzo, E.21
Martini, C.22
Brancale, A.23
Marinelli, L.24
Novellino, E.25
Vultaggio, S.26
Varasi, M.27
Mercurio, C.28
Bigogno, C.29
Dondio, G.30
Hamel, E.31
Lavia, P.32
Silvestri, R.33
more..
-
71
-
-
84876236530
-
Endowing indole-based tubulin inhibitors with an anchor for derivatization: Highly potent 3-substituted indolephenstatins and indoleisocombretastatins
-
álvarez, R.; Puebla, P.; Díaz, J. F.; Bento, A. C.; García-Navas, R.; de la Iglesia-Vicente, J.; Mollinedo, F.; Andreu, J. M.; Medarde, M.; Peláez, R. Endowing indole-based tubulin inhibitors with an anchor for derivatization: highly potent 3-substituted indolephenstatins and indoleisocombretastatins J. Med. Chem. 2013, 56, 2813-2827 10.1021/jm3015603
-
(2013)
J. Med. Chem.
, vol.56
, pp. 2813-2827
-
-
Álvarez, R.1
Puebla, P.2
Díaz, J.F.3
Bento, A.C.4
García-Navas, R.5
De La Iglesia-Vicente, J.6
Mollinedo, F.7
Andreu, J.M.8
Medarde, M.9
Peláez, R.10
-
72
-
-
79960151500
-
Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl- thiazoles analogues as potent and orally bioavailable anticancer agents
-
Lu, Y.; Li, C. M.; Wang, Z.; Chen, J.; Mohler, M. L.; Li, W.; Dalton, J. T.; Miller, D. D. Design, synthesis, and SAR studies of 4-substituted methoxylbenzoyl-aryl- thiazoles analogues as potent and orally bioavailable anticancer agents J. Med. Chem. 2011, 54, 4678-4693 10.1021/jm2003427
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4678-4693
-
-
Lu, Y.1
Li, C.M.2
Wang, Z.3
Chen, J.4
Mohler, M.L.5
Li, W.6
Dalton, J.T.7
Miller, D.D.8
-
73
-
-
84906094556
-
New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including Hedgehog-dependent cancer
-
La Regina, G.; Bai, R.; Coluccia, A.; Famiglini, V.; Pelliccia, S.; Passacantilli, S.; Mazzoccoli, C.; Ruggieri, V.; Sisinni, L.; Bolognesi, A.; Rensen, W. M.; Miele, A.; Nalli, M.; Alfonsi, R.; Di Marcotullio, L.; Gulino, A.; Brancale, A.; Novellino, E.; Dondio, G.; Vultaggio, S.; Varasi, M.; Mercurio, C.; Hamel, E.; Lavia, P.; Silvestri, R. New pyrrole derivatives with potent tubulin polymerization inhibiting activity as anticancer agents including Hedgehog-dependent cancer J. Med. Chem. 2014, 57, 6531-6552 10.1021/jm500561a
-
(2014)
J. Med. Chem.
, vol.57
, pp. 6531-6552
-
-
La Regina, G.1
Bai, R.2
Coluccia, A.3
Famiglini, V.4
Pelliccia, S.5
Passacantilli, S.6
Mazzoccoli, C.7
Ruggieri, V.8
Sisinni, L.9
Bolognesi, A.10
Rensen, W.M.11
Miele, A.12
Nalli, M.13
Alfonsi, R.14
Di Marcotullio, L.15
Gulino, A.16
Brancale, A.17
Novellino, E.18
Dondio, G.19
Vultaggio, S.20
Varasi, M.21
Mercurio, C.22
Hamel, E.23
Lavia, P.24
Silvestri, R.25
more..
-
74
-
-
84906094647
-
Synthesis, antimitotic and antivascular activity of 1-(3′,4′,5′-trimethoxybenzoyl)-3-arylamino-5-amino-1,2,4-triazoles
-
Romagnoli, R.; Baraldi, P. G.; Salvador, M. K.; Prencipe, F.; Bertolasi, V.; Cancellieri, M.; Brancale, A.; Hamel, E.; Castagliuolo, I.; Consolaro, F.; Porcù, E.; Basso, G.; Viola, G. Synthesis, antimitotic and antivascular activity of 1-(3′,4′,5′-trimethoxybenzoyl)-3-arylamino-5-amino-1,2,4-triazoles J. Med. Chem. 2014, 57, 6795-6808 10.1021/jm5008193
-
(2014)
J. Med. Chem.
, vol.57
, pp. 6795-6808
-
-
Romagnoli, R.1
Baraldi, P.G.2
Salvador, M.K.3
Prencipe, F.4
Bertolasi, V.5
Cancellieri, M.6
Brancale, A.7
Hamel, E.8
Castagliuolo, I.9
Consolaro, F.10
Porcù, E.11
Basso, G.12
Viola, G.13
-
75
-
-
84946570782
-
Chalcones as promising lead compounds on cancer therapy
-
León-González, A. J.; Acero, N.; Muñoz-Mingarro, D.; Navarro, I.; Martín-Cordero, C. Chalcones as promising lead compounds on cancer therapy Curr. Med. Chem. 2015, 22, 3407-3425 10.2174/0929867322666150729114829
-
(2015)
Curr. Med. Chem.
, vol.22
, pp. 3407-3425
-
-
León-González, A.J.1
Acero, N.2
Muñoz-Mingarro, D.3
Navarro, I.4
Martín-Cordero, C.5
-
76
-
-
65549090501
-
Antimitotic chalcones and related compounds as inhibitors of tubulin assembly
-
Ducki, S. Antimitotic chalcones and related compounds as inhibitors of tubulin assembly Anti-Cancer Agents Med. Chem. 2009, 9, 336-347 10.2174/1871520610909030336
-
(2009)
Anti-Cancer Agents Med. Chem.
, vol.9
, pp. 336-347
-
-
Ducki, S.1
-
77
-
-
72049087235
-
Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 1: Synthesis and biological evaluation of antivascular activity
-
Ducki, S.; Rennison, D.; Woo, M.; Kendall, A.; Chabert, J. F. D.; McGown, A. T.; Lawrence, N. J. Combretastatin-like chalcones as inhibitors of microtubule polymerization. Part 1: Synthesis and biological evaluation of antivascular activity Bioorg. Med. Chem. 2009, 17, 7698-7710 10.1016/j.bmc.2009.09.039
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 7698-7710
-
-
Ducki, S.1
Rennison, D.2
Woo, M.3
Kendall, A.4
Chabert, J.F.D.5
McGown, A.T.6
Lawrence, N.J.7
-
78
-
-
84906094004
-
Discovery of potent cytotoxic ortho-aryl chalcones as new scaffold targeting tubulin and mitosis with affinity-based fluorescence
-
Zhu, C.; Zuo, Y.; Wang, R.; Liang, B.; Yue, X.; Wen, G.; Shang, N.; Huang, L.; Chen, Y.; Du, J.; Bu, X. Discovery of potent cytotoxic ortho-aryl chalcones as new scaffold targeting tubulin and mitosis with affinity-based fluorescence J. Med. Chem. 2014, 57, 6364-6382 10.1021/jm500024v
-
(2014)
J. Med. Chem.
, vol.57
, pp. 6364-6382
-
-
Zhu, C.1
Zuo, Y.2
Wang, R.3
Liang, B.4
Yue, X.5
Wen, G.6
Shang, N.7
Huang, L.8
Chen, Y.9
Du, J.10
Bu, X.11
-
79
-
-
84931097556
-
IPP51, a chalcone acting as a microtubule inhibitor with in vivo antitumor activity against bladder carcinoma
-
Martel-Frachet, V.; Keramidas, M.; Nurisso, A.; DeBonis, S.; Rome, C.; Coll, J. L.; Boumendjel, A.; Skoufias, D. A.; Ronot, X. IPP51, a chalcone acting as a microtubule inhibitor with in vivo antitumor activity against bladder carcinoma Oncotarget 2015, 6, 14669-14686 10.18632/oncotarget.4144
-
(2015)
Oncotarget
, vol.6
, pp. 14669-14686
-
-
Martel-Frachet, V.1
Keramidas, M.2
Nurisso, A.3
DeBonis, S.4
Rome, C.5
Coll, J.L.6
Boumendjel, A.7
Skoufias, D.A.8
Ronot, X.9
-
80
-
-
84899581962
-
Design, synthesis, and biological evaluation of novel pyridine-bridged analogues of combretastatin-A4 as anticancer agents
-
Zheng, S.; Zhong, Q.; Mottamal, M.; Zhang, Q.; Zhang, C.; LeMelle, E.; McFerrin, H.; Wang, G. Design, synthesis, and biological evaluation of novel pyridine-bridged analogues of combretastatin-A4 as anticancer agents J. Med. Chem. 2014, 57, 3369-3381 10.1021/jm500002k
-
(2014)
J. Med. Chem.
, vol.57
, pp. 3369-3381
-
-
Zheng, S.1
Zhong, Q.2
Mottamal, M.3
Zhang, Q.4
Zhang, C.5
LeMelle, E.6
McFerrin, H.7
Wang, G.8
-
81
-
-
0030756156
-
Mechanism of action of E7010, an orally active sulfonamide antitumor agent: Inhibition of mitosis by binding to the colchicine site of tubulin
-
Yoshimatsu, K.; Yamaguchi, A.; Yoshino, H.; Koyanagi, N.; Kitoh, K. Mechanism of action of E7010, an orally active sulfonamide antitumor agent: inhibition of mitosis by binding to the colchicine site of tubulin Cancer Res. 1997, 57, 3208-3213
-
(1997)
Cancer Res.
, vol.57
, pp. 3208-3213
-
-
Yoshimatsu, K.1
Yamaguchi, A.2
Yoshino, H.3
Koyanagi, N.4
Kitoh, K.5
-
82
-
-
33646741205
-
The pharmacokinetics and safety of ABT-751, a novel, orally bioavailable sulfonamide antimitotic agent: Results of a phase 1 study
-
Hande, K. R.; Hagey, A.; Berlin, J.; Cai, Y.; Meek, K.; Kobayashi, H.; Lockhart, A. C.; Medina, D.; Sosman, J.; Gordon, G. B.; Rothenberg, M. L. The pharmacokinetics and safety of ABT-751, a novel, orally bioavailable sulfonamide antimitotic agent: results of a phase 1 study Clin. Cancer Res. 2006, 12, 2834-2840 10.1158/1078-0432.CCR-05-2159
-
(2006)
Clin. Cancer Res.
, vol.12
, pp. 2834-2840
-
-
Hande, K.R.1
Hagey, A.2
Berlin, J.3
Cai, Y.4
Meek, K.5
Kobayashi, H.6
Lockhart, A.C.7
Medina, D.8
Sosman, J.9
Gordon, G.B.10
Rothenberg, M.L.11
-
83
-
-
69549122767
-
Variations in the colchicine-binding domain provide insight into the structural switch of tubulin
-
Dorléans, A.; Gigant, B.; Ravelli, R. B.; Mailliet, P.; Mikol, V.; Knossow, M. Variations in the colchicine-binding domain provide insight into the structural switch of tubulin Proc. Natl. Acad. Sci. U. S. A. 2009, 106, 13775-13779 10.1073/pnas.0904223106
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 13775-13779
-
-
Dorléans, A.1
Gigant, B.2
Ravelli, R.B.3
Mailliet, P.4
Mikol, V.5
Knossow, M.6
-
84
-
-
33750976393
-
7-Aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents
-
Chang, J. Y.; Hsieh, H. P.; Chang, C. Y.; Hsu, K. S.; Chiang, Y. F.; Chen, C. M.; Kuo, C. C.; Liou, J. P. 7-Aroyl-aminoindoline-1-sulfonamides as a novel class of potent antitubulin agents J. Med. Chem. 2006, 49, 6656-6659 10.1021/jm061076u
-
(2006)
J. Med. Chem.
, vol.49
, pp. 6656-6659
-
-
Chang, J.Y.1
Hsieh, H.P.2
Chang, C.Y.3
Hsu, K.S.4
Chiang, Y.F.5
Chen, C.M.6
Kuo, C.C.7
Liou, J.P.8
-
85
-
-
33646118484
-
NPI-2358 is a tubulin-depolymerizing agent: In-vitro evidence for activity as a tumor vascular-disrupting agent
-
Nicholson, B.; Lloyd, G. K.; Miller, B. R.; Palladino, M. A.; Kiso, Y.; Hayashi, Y.; Neuteboom, S. T. C. NPI-2358 is a tubulin-depolymerizing agent: in-vitro evidence for activity as a tumor vascular-disrupting agent Anti-Cancer Drugs 2006, 17, 25-31 10.1097/01.cad.0000182745.01612.8a
-
(2006)
Anti-Cancer Drugs
, vol.17
, pp. 25-31
-
-
Nicholson, B.1
Lloyd, G.K.2
Miller, B.R.3
Palladino, M.A.4
Kiso, Y.5
Hayashi, Y.6
Neuteboom, S.T.C.7
-
86
-
-
77951206196
-
Anti-microtubule "plinabulin' chemical probe KPU-244-B3 labeled both α- And β-tubulin
-
Yamazaki, Y.; Sumikura, M.; Hidaka, K.; Yasui, H.; Kiso, Y.; Yakushiji, F.; Hayashi, Y. Anti-microtubule "plinabulin' chemical probe KPU-244-B3 labeled both α- and β-tubulin Bioorg. Med. Chem. 2010, 18, 3169-3174 10.1016/j.bmc.2010.03.037
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 3169-3174
-
-
Yamazaki, Y.1
Sumikura, M.2
Hidaka, K.3
Yasui, H.4
Kiso, Y.5
Yakushiji, F.6
Hayashi, Y.7
-
87
-
-
78650751998
-
Tubulin photoaffinity labeling study with a plinabulin chemical probe possessing a biotin tag at the oxazole
-
Yamazaki, Y.; Kido, Y.; Hidaka, K.; Yasui, H.; Kiso, Y.; Yakushiji, F.; Hayashi, Y. Tubulin photoaffinity labeling study with a plinabulin chemical probe possessing a biotin tag at the oxazole Bioorg. Med. Chem. 2011, 19, 595-602 10.1016/j.bmc.2010.10.055
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 595-602
-
-
Yamazaki, Y.1
Kido, Y.2
Hidaka, K.3
Yasui, H.4
Kiso, Y.5
Yakushiji, F.6
Hayashi, Y.7
-
88
-
-
84961285450
-
Structures of a diverse set of colchicine binding site inhibitors in complex with tubulin provide a rationale for drug discovery
-
Wang, Y.; Zhang, H.; Gigant, B.; Yu, Y.; Wu, Y.; Chen, X.; Lai, Q.; Yang, Z.; Chen, Q.; Yang, J. Structures of a diverse set of colchicine binding site inhibitors in complex with tubulin provide a rationale for drug discovery FEBS J. 2016, 283, 102-111 10.1111/febs.13555
-
(2016)
FEBS J.
, vol.283
, pp. 102-111
-
-
Wang, Y.1
Zhang, H.2
Gigant, B.3
Yu, Y.4
Wu, Y.5
Chen, X.6
Lai, Q.7
Yang, Z.8
Chen, Q.9
Yang, J.10
-
89
-
-
84863158929
-
Synthesis and structure-activity relationship study of antimicrotubule agents phenylahistin derivatives with a didehydropiperazine-2,5-dione structure
-
Yamazaki, Y.; Tanaka, K.; Nicholson, B.; Deyanat-Yazdi, G.; Potts, B.; Yoshida, T.; Oda, A.; Kitagawa, T.; Orikasa, S.; Kiso, Y.; Yasui, H.; Akamatsu, M.; Chinen, T.; Usui, T.; Shinozaki, Y.; Yakushiji, F.; Miller, B. R.; Neuteboom, S.; Palladino, M.; Kanoh, K.; Lloyd, G. K.; Hayashi, Y. Synthesis and structure-activity relationship study of antimicrotubule agents phenylahistin derivatives with a didehydropiperazine-2,5-dione structure J. Med. Chem. 2012, 55, 1056-1071 10.1021/jm2009088
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1056-1071
-
-
Yamazaki, Y.1
Tanaka, K.2
Nicholson, B.3
Deyanat-Yazdi, G.4
Potts, B.5
Yoshida, T.6
Oda, A.7
Kitagawa, T.8
Orikasa, S.9
Kiso, Y.10
Yasui, H.11
Akamatsu, M.12
Chinen, T.13
Usui, T.14
Shinozaki, Y.15
Yakushiji, F.16
Miller, B.R.17
Neuteboom, S.18
Palladino, M.19
Kanoh, K.20
Lloyd, G.K.21
Hayashi, Y.22
more..
-
90
-
-
58149096782
-
Synthesis and structure-activity relationships of 2-amino-1-aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents
-
Reddy, G. R.; Kuo, C.-C.; Tan, U.-K.; Coumar, M. S.; Chang, C.-Y.; Chiang, Y.-K.; Lai, M.-J.; Yeh, J.-Y.; Wu, S.-Y.; Chang, J.-Y.; Liou, J.-P.; Hsieh, H.-P. Synthesis and structure-activity relationships of 2-amino-1-aroylnaphthalene and 2-hydroxy-1-aroylnaphthalenes as potent antitubulin agents J. Med. Chem. 2008, 51, 8163-8167 10.1021/jm8008635
-
(2008)
J. Med. Chem.
, vol.51
, pp. 8163-8167
-
-
Reddy, G.R.1
Kuo, C.-C.2
Tan, U.-K.3
Coumar, M.S.4
Chang, C.-Y.5
Chiang, Y.-K.6
Lai, M.-J.7
Yeh, J.-Y.8
Wu, S.-Y.9
Chang, J.-Y.10
Liou, J.-P.11
Hsieh, H.-P.12
-
91
-
-
67651112008
-
Discovery of CYT997: A structurally novel orally active microtubule targeting agent
-
Burns, C. J.; Harte, M. F.; Bu, X.; Fantino, E.; Joffe, M.; Sikanyika, H.; Su, S.; Tranberg, C. E.; Wilson, N.; Charman, S. A.; Shackleford, D. M.; Wilks, A. F. Discovery of CYT997: a structurally novel orally active microtubule targeting agent Bioorg. Med. Chem. Lett. 2009, 19, 4639-4642 10.1016/j.bmcl.2009.06.079
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4639-4642
-
-
Burns, C.J.1
Harte, M.F.2
Bu, X.3
Fantino, E.4
Joffe, M.5
Sikanyika, H.6
Su, S.7
Tranberg, C.E.8
Wilson, N.9
Charman, S.A.10
Shackleford, D.M.11
Wilks, A.F.12
-
92
-
-
70949094381
-
CYT997: A novel orally active tubulin polymerization inhibitor with potent cytotoxic and vascular disrupting activity in vitro and in vivo
-
Burns, C. J.; Fantino, E.; Phillips, I. D.; Su, S.; Harte, M. F.; Bukczynska, P. E.; Frazzetto, M.; Joffe, M.; Kruszelnicki, I.; Wang, B.; Wang, Y.; Wilson, N.; Dilley, R. J.; Wan, S. S.; Charman, S. A.; Shackleford, D. M.; Fida, R.; Malcontenti-Wilson, C.; Wilks, A. F. CYT997: a novel orally active tubulin polymerization inhibitor with potent cytotoxic and vascular disrupting activity in vitro and in vivo Mol. Cancer Ther. 2009, 8, 3036-3045 10.1158/1535-7163.MCT-09-0076
-
(2009)
Mol. Cancer Ther.
, vol.8
, pp. 3036-3045
-
-
Burns, C.J.1
Fantino, E.2
Phillips, I.D.3
Su, S.4
Harte, M.F.5
Bukczynska, P.E.6
Frazzetto, M.7
Joffe, M.8
Kruszelnicki, I.9
Wang, B.10
Wang, Y.11
Wilson, N.12
Dilley, R.J.13
Wan, S.S.14
Charman, S.A.15
Shackleford, D.M.16
Fida, R.17
Malcontenti-Wilson, C.18
Wilks, A.F.19
-
93
-
-
0035133804
-
D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity
-
Bacher, G.; Nickel, B.; Emig, P.; Vanhoefer, U.; Seeber, S.; Shandra, A.; Klenner, T.; Beckers, T. D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity Cancer Res. 2001, 61, 392-399
-
(2001)
Cancer Res.
, vol.61
, pp. 392-399
-
-
Bacher, G.1
Nickel, B.2
Emig, P.3
Vanhoefer, U.4
Seeber, S.5
Shandra, A.6
Klenner, T.7
Beckers, T.8
-
94
-
-
77952241570
-
Dose-finding and pharmacokinetic study of orally administered indibulin (D-24851) to patients with advanced solid tumors
-
Oostendorp, R. L.; Witteveen, P. O.; Schwartz, B.; Vainchtein, L. D.; Schot, M.; Nol, A.; Rosing, H.; Beijnen, J. H.; Voest, E. E.; Schellens, J. H. M. Dose-finding and pharmacokinetic study of orally administered indibulin (D-24851) to patients with advanced solid tumors Invest. New Drugs 2010, 28, 163-170 10.1007/s10637-009-9244-6
-
(2010)
Invest. New Drugs
, vol.28
, pp. 163-170
-
-
Oostendorp, R.L.1
Witteveen, P.O.2
Schwartz, B.3
Vainchtein, L.D.4
Schot, M.5
Nol, A.6
Rosing, H.7
Beijnen, J.H.8
Voest, E.E.9
Schellens, J.H.M.10
-
95
-
-
84949843853
-
An orally bioavailable, indole-3-glyoxylamide based series of tubulin polymerization inhibitors showing tumor growth inhibition in a mouse xenograft model of head and neck cancer
-
Colley, H. E.; Muthana, M.; Danson, S. J.; Jackson, L. V.; Brett, M. L.; Harrison, J.; Coole, S. F.; Mason, D. P.; Jennings, L. R.; Wong, M.; Tulasi, V.; Norman, D.; Lockey, P. M.; Williams, L.; Dossetter, A. G.; Griffen, E. J.; Thompson, M. J. An orally bioavailable, indole-3-glyoxylamide based series of tubulin polymerization inhibitors showing tumor growth inhibition in a mouse xenograft model of head and neck cancer J. Med. Chem. 2015, 58, 9309-9333 10.1021/acs.jmedchem.5b01312
-
(2015)
J. Med. Chem.
, vol.58
, pp. 9309-9333
-
-
Colley, H.E.1
Muthana, M.2
Danson, S.J.3
Jackson, L.V.4
Brett, M.L.5
Harrison, J.6
Coole, S.F.7
Mason, D.P.8
Jennings, L.R.9
Wong, M.10
Tulasi, V.11
Norman, D.12
Lockey, P.M.13
Williams, L.14
Dossetter, A.G.15
Griffen, E.J.16
Thompson, M.J.17
-
96
-
-
80054743497
-
A phase i study of MN-029 (denibulin), a novel vascular-disrupting agent, in patients with advanced solid tumors
-
Ricart, A. D.; Ashton, E. A.; Cooney, M. M.; Sarantopoulos, J.; Brell, J. M.; Feldman, M. A.; Ruby, K. E.; Matsuda, K.; Munsey, M. S.; Medina, G.; Zambito, A.; Tolcher, A. W.; Remick, S. C. A phase I study of MN-029 (denibulin), a novel vascular-disrupting agent, in patients with advanced solid tumors Cancer Chemother. Pharmacol. 2011, 68, 959-970 10.1007/s00280-011-1565-4
-
(2011)
Cancer Chemother. Pharmacol.
, vol.68
, pp. 959-970
-
-
Ricart, A.D.1
Ashton, E.A.2
Cooney, M.M.3
Sarantopoulos, J.4
Brell, J.M.5
Feldman, M.A.6
Ruby, K.E.7
Matsuda, K.8
Munsey, M.S.9
Medina, G.10
Zambito, A.11
Tolcher, A.W.12
Remick, S.C.13
-
97
-
-
34250859583
-
MPC-6827: A small-molecule inhibitor of microtubule formation that is not a substrate for multidrug resistance pumps
-
Kasibhatla, S.; Baichwal, V.; Cai, S. X.; Roth, B.; Skvortsova, I.; Skvortsov, S.; Lukas, P.; English, N. M.; Sirisoma, N.; Drewe, J.; Pervin, A.; Tseng, B.; Carlson, R. O.; Pleiman, C. M. MPC-6827: a small-molecule inhibitor of microtubule formation that is not a substrate for multidrug resistance pumps Cancer Res. 2007, 67, 5865-5871 10.1158/0008-5472.CAN-07-0127
-
(2007)
Cancer Res.
, vol.67
, pp. 5865-5871
-
-
Kasibhatla, S.1
Baichwal, V.2
Cai, S.X.3
Roth, B.4
Skvortsova, I.5
Skvortsov, S.6
Lukas, P.7
English, N.M.8
Sirisoma, N.9
Drewe, J.10
Pervin, A.11
Tseng, B.12
Carlson, R.O.13
Pleiman, C.M.14
-
98
-
-
65149091722
-
Discovery of N-(4-methoxyphenyl)-N,2-dimethylquinazolin-4-amine, a potent apoptosis inducer and efficacious anticancer agent with high blood brain barrier penetration
-
Sirisoma, N.; Pervin, A.; Zhang, H.; Jiang, S.; Willardsen, J. A.; Anderson, M. B.; Mather, G.; Pleiman, C. M.; Kasibhatla, S.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of N-(4-methoxyphenyl)-N,2-dimethylquinazolin-4-amine, a potent apoptosis inducer and efficacious anticancer agent with high blood brain barrier penetration J. Med. Chem. 2009, 52, 2341-2351 10.1021/jm801315b
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2341-2351
-
-
Sirisoma, N.1
Pervin, A.2
Zhang, H.3
Jiang, S.4
Willardsen, J.A.5
Anderson, M.B.6
Mather, G.7
Pleiman, C.M.8
Kasibhatla, S.9
Tseng, B.10
Drewe, J.11
Cai, S.X.12
-
99
-
-
84907848614
-
Synthesis and antiproliferative activity of 6-phenylaminopurines
-
Canela, M. D.; Liekens, S.; Camarasa, M. J.; Priego, E. M.; Pérez-Pérez, M. J. Synthesis and antiproliferative activity of 6-phenylaminopurines Eur. J. Med. Chem. 2014, 87, 421-428 10.1016/j.ejmech.2014.09.093
-
(2014)
Eur. J. Med. Chem.
, vol.87
, pp. 421-428
-
-
Canela, M.D.1
Liekens, S.2
Camarasa, M.J.3
Priego, E.M.4
Pérez-Pérez, M.J.5
-
100
-
-
78649509037
-
Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance
-
Gangjee, A.; Zhao, Y.; Lin, L.; Raghavan, S.; Roberts, E. G.; Risinger, A. L.; Hamel, E.; Mooberry, S. L. Synthesis and discovery of water-soluble microtubule targeting agents that bind to the colchicine site on tubulin and circumvent Pgp mediated resistance J. Med. Chem. 2010, 53, 8116-8128 10.1021/jm101010n
-
(2010)
J. Med. Chem.
, vol.53
, pp. 8116-8128
-
-
Gangjee, A.1
Zhao, Y.2
Lin, L.3
Raghavan, S.4
Roberts, E.G.5
Risinger, A.L.6
Hamel, E.7
Mooberry, S.L.8
-
101
-
-
84902536299
-
The design and discovery of water soluble 4-substituted-2,6-dimethylfuro[2, 3-d]pyrimidines as multitargeted receptor tyrosine kinase inhibitors and microtubule targeting antitumor agents
-
Zhang, X.; Raghavan, S.; Ihnat, M.; Thorpe, J. E.; Disch, B. C.; Bastian, A.; Bailey-Downs, L. C.; Dybdal-Hargreaves, N. F.; Rohena, C. C.; Hamel, E.; Mooberry, S. L.; Gangjee, A. The design and discovery of water soluble 4-substituted-2,6-dimethylfuro[2, 3-d]pyrimidines as multitargeted receptor tyrosine kinase inhibitors and microtubule targeting antitumor agents Bioorg. Med. Chem. 2014, 22, 3753-3772 10.1016/j.bmc.2014.04.049
-
(2014)
Bioorg. Med. Chem.
, vol.22
, pp. 3753-3772
-
-
Zhang, X.1
Raghavan, S.2
Ihnat, M.3
Thorpe, J.E.4
Disch, B.C.5
Bastian, A.6
Bailey-Downs, L.C.7
Dybdal-Hargreaves, N.F.8
Rohena, C.C.9
Hamel, E.10
Mooberry, S.L.11
Gangjee, A.12
-
102
-
-
0028331925
-
2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site
-
D'Amato, R. J.; Lin, C. M.; Flynn, E.; Folkman, J.; Hamel, E. 2-Methoxyestradiol, an endogenous mammalian metabolite, inhibits tubulin polymerization by interacting at the colchicine site Proc. Natl. Acad. Sci. U. S. A. 1994, 91, 3964-3968 10.1073/pnas.91.9.3964
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 3964-3968
-
-
D'Amato, R.J.1
Lin, C.M.2
Flynn, E.3
Folkman, J.4
Hamel, E.5
-
103
-
-
33845953699
-
2-Substituted estradiol bis-sulfamates, multitargeted antitumor agents: Synthesis, in vitro SAR, protein crystallography, and in vivo activity
-
Leese, M. P.; Leblond, B.; Smith, A.; Newman, S. P.; Di Fiore, A.; De Simone, G.; Supuran, C. T.; Purohit, A.; Reed, M. J.; Potter, B. V. L. 2-Substituted estradiol bis-sulfamates, multitargeted antitumor agents: synthesis, in vitro SAR, protein crystallography, and in vivo activity J. Med. Chem. 2006, 49, 7683-7696 10.1021/jm060705x
-
(2006)
J. Med. Chem.
, vol.49
, pp. 7683-7696
-
-
Leese, M.P.1
Leblond, B.2
Smith, A.3
Newman, S.P.4
Di Fiore, A.5
De Simone, G.6
Supuran, C.T.7
Purohit, A.8
Reed, M.J.9
Potter, B.V.L.10
-
104
-
-
84942800995
-
The in vitro and in vivo activity of the microtubule disruptor STX140 is mediated by HIF-1 alpha and CAIX expression
-
Stengel, C.; Newman, S. P.; Leese, M. P.; Thomas, M. P.; Potter, B. V. L; Reed, M. J.; Purohit, A.; Foster, P. A. The in vitro and in vivo activity of the microtubule disruptor STX140 is mediated by HIF-1 alpha and CAIX expression Anticancer Res. 2015, 35, 5249-5262
-
(2015)
Anticancer Res.
, vol.35
, pp. 5249-5262
-
-
Stengel, C.1
Newman, S.P.2
Leese, M.P.3
Thomas, M.P.4
Potter, B.V.L.5
Reed, M.J.6
Purohit, A.7
Foster, P.A.8
-
105
-
-
84863422019
-
Steroidomimetic tetrahydroisoquinolines for the design of new microtubule disruptors
-
Leese, M. P.; Jourdan, F.; Dohle, W.; Kimberley, M. R.; Thomas, M. P.; Bai, R.; Hamel, E.; Ferrandis, E.; Potter, B. V. L. Steroidomimetic tetrahydroisoquinolines for the design of new microtubule disruptors ACS Med. Chem. Lett. 2012, 3, 5-9 10.1021/ml200232c
-
(2012)
ACS Med. Chem. Lett.
, vol.3
, pp. 5-9
-
-
Leese, M.P.1
Jourdan, F.2
Dohle, W.3
Kimberley, M.R.4
Thomas, M.P.5
Bai, R.6
Hamel, E.7
Ferrandis, E.8
Potter, B.V.L.9
-
106
-
-
77952123093
-
ENMD-1198, a new analogue of 2-methoxyestradiol, displays both antiangiogenic and vascular-disrupting properties
-
Pasquier, E.; Sinnappan, S.; Munoz, M. A.; Kavallaris, M. ENMD-1198, a new analogue of 2-methoxyestradiol, displays both antiangiogenic and vascular-disrupting properties Mol. Cancer Ther. 2010, 9, 1408-1418 10.1158/1535-7163.MCT-09-0894
-
(2010)
Mol. Cancer Ther.
, vol.9
, pp. 1408-1418
-
-
Pasquier, E.1
Sinnappan, S.2
Munoz, M.A.3
Kavallaris, M.4
-
107
-
-
0032495513
-
Structure of the αβ tubulin dimer by electron crystallography
-
Nogales, E.; Wolf, S. G.; Downing, K. H. Structure of the αβ tubulin dimer by electron crystallography Nature 1998, 391, 199-203 10.1038/34465
-
(1998)
Nature
, vol.391
, pp. 199-203
-
-
Nogales, E.1
Wolf, S.G.2
Downing, K.H.3
-
108
-
-
0035834521
-
Refined structure of α,β-tubulin at 3.5 Å resolution
-
Löwe, J.; Li, H.; Downing, K. H.; Nogales, E. Refined structure of α,β-tubulin at 3.5 Å resolution J. Mol. Biol. 2001, 313, 1045-1057 10.1006/jmbi.2001.5077
-
(2001)
J. Mol. Biol.
, vol.313
, pp. 1045-1057
-
-
Löwe, J.1
Li, H.2
Downing, K.H.3
Nogales, E.4
-
109
-
-
84906491034
-
The tubulin code Molecular components, readout mechanisms, and functions
-
Janke, C. The tubulin code Molecular components, readout mechanisms, and functions J. Cell Biol. 2014, 206, 461-472 10.1083/jcb.201406055
-
(2014)
J. Cell Biol.
, vol.206
, pp. 461-472
-
-
Janke, C.1
-
110
-
-
0034664244
-
The 4 Å X-Ray structure of a tubulin:stathmin-like domain complex
-
Gigant, B.; Curmi, P. A.; Martin-Barbey, C.; Charbaut, E.; Lachkar, S.; Lebeau, L.; Siavoshian, S.; Sobel, A.; Knossow, M. The 4 Å X-Ray structure of a tubulin:stathmin-like domain complex Cell 2000, 102, 809-816 10.1016/S0092-8674(00)00069-6
-
(2000)
Cell
, vol.102
, pp. 809-816
-
-
Gigant, B.1
Curmi, P.A.2
Martin-Barbey, C.3
Charbaut, E.4
Lachkar, S.5
Lebeau, L.6
Siavoshian, S.7
Sobel, A.8
Knossow, M.9
-
111
-
-
77957763787
-
Stathmin and interfacial microtubule inhibitors recognize a naturally curved conformation of tubulin dimers
-
Barbier, P.; Dorléans, A.; Devred, F.; Sanz, L.; Allegro, D.; Alfonso, C.; Knossow, M.; Peyrot, V.; Andreu, J. M. Stathmin and interfacial microtubule inhibitors recognize a naturally curved conformation of tubulin dimers J. Biol. Chem. 2010, 285, 31672-31681 10.1074/jbc.M110.141929
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 31672-31681
-
-
Barbier, P.1
Dorléans, A.2
Devred, F.3
Sanz, L.4
Allegro, D.5
Alfonso, C.6
Knossow, M.7
Peyrot, V.8
Andreu, J.M.9
-
112
-
-
0016816834
-
Incorporation of L-tyrosine, L-phenylalanine and L-3,4-dihydroxyphenylalanine as single units into rat-brain tubulin
-
Arce, C. A.; Rodriguez, J. A.; Barra, H. S.; Caputto, R. Incorporation of L-tyrosine, L-phenylalanine and L-3,4-dihydroxyphenylalanine as single units into rat-brain tubulin Eur. J. Biochem. 1975, 59, 145-149 10.1111/j.1432-1033.1975.tb02435.x
-
(1975)
Eur. J. Biochem.
, vol.59
, pp. 145-149
-
-
Arce, C.A.1
Rodriguez, J.A.2
Barra, H.S.3
Caputto, R.4
-
113
-
-
84874362901
-
Structural basis of tubulin tyrosination by tubulin tyrosine ligase
-
Prota, A. E.; Magiera, M. M.; Kuijpers, M.; Bargsten, K.; Frey, D.; Wieser, M.; Jaussi, R.; Hoogenraad, C. C.; Kammerer, R. A.; Janke, C.; Steinmetz, M. O. Structural basis of tubulin tyrosination by tubulin tyrosine ligase J. Cell Biol. 2013, 200, 259-270 10.1083/jcb.201211017
-
(2013)
J. Cell Biol.
, vol.200
, pp. 259-270
-
-
Prota, A.E.1
Magiera, M.M.2
Kuijpers, M.3
Bargsten, K.4
Frey, D.5
Wieser, M.6
Jaussi, R.7
Hoogenraad, C.C.8
Kammerer, R.A.9
Janke, C.10
Steinmetz, M.O.11
-
114
-
-
84873090491
-
Molecular mechanism of action of microtubule-stabilizing anticancer agents
-
Prota, A. E.; Bargsten, K.; Zurwerra, D.; Field, J. J.; Diaz, J. F.; Altmann, K.-H.; Steinmetz, M. O. Molecular mechanism of action of microtubule-stabilizing anticancer agents Science 2013, 339, 587-590 10.1126/science.1230582
-
(2013)
Science
, vol.339
, pp. 587-590
-
-
Prota, A.E.1
Bargsten, K.2
Zurwerra, D.3
Field, J.J.4
Diaz, J.F.5
Altmann, K.-H.6
Steinmetz, M.O.7
-
115
-
-
84897109910
-
The novel microtubule-destabilizing drug BAL27862 binds to the colchicine site of tubulin with distinct effects on microtubule organization
-
Prota, A. E.; Danel, F.; Bachmann, F.; Bargsten, K.; Buey, R. M.; Pohlmann, J.; Reinelt, S.; Lane, H.; Steinmetz, M. O. The novel microtubule-destabilizing drug BAL27862 binds to the colchicine site of tubulin with distinct effects on microtubule organization J. Mol. Biol. 2014, 426, 1848-1860 10.1016/j.jmb.2014.02.005
-
(2014)
J. Mol. Biol.
, vol.426
, pp. 1848-1860
-
-
Prota, A.E.1
Danel, F.2
Bachmann, F.3
Bargsten, K.4
Buey, R.M.5
Pohlmann, J.6
Reinelt, S.7
Lane, H.8
Steinmetz, M.O.9
-
116
-
-
84907270556
-
A new tubulin-binding site and pharmacophore for microtubule-destabilizing anticancer drugs
-
Prota, A. E.; Bargsten, K.; Diaz, J. F.; Marsh, M.; Cuevas, C.; Liniger, M.; Neuhaus, C.; Andreu, J. M.; Altmann, K.-H.; Steinmetz, M. O. A new tubulin-binding site and pharmacophore for microtubule-destabilizing anticancer drugs Proc. Natl. Acad. Sci. U. S. A. 2014, 111, 13817-13821 10.1073/pnas.1408124111
-
(2014)
Proc. Natl. Acad. Sci. U. S. A.
, vol.111
, pp. 13817-13821
-
-
Prota, A.E.1
Bargsten, K.2
Diaz, J.F.3
Marsh, M.4
Cuevas, C.5
Liniger, M.6
Neuhaus, C.7
Andreu, J.M.8
Altmann, K.-H.9
Steinmetz, M.O.10
-
117
-
-
84946012049
-
Structures of potent anticancer compounds bound to tubulin
-
McNamara, D. E.; Senese, S.; Yeates, T. O.; Torres, J. Z. Structures of potent anticancer compounds bound to tubulin Protein Sci. 2015, 24, 1164-1172 10.1002/pro.2704
-
(2015)
Protein Sci.
, vol.24
, pp. 1164-1172
-
-
McNamara, D.E.1
Senese, S.2
Yeates, T.O.3
Torres, J.Z.4
-
118
-
-
0346962971
-
Structural interaction fingerprint (SIFt): A novel method for analyzing three-dimensional protein-ligand binding interactions
-
Deng, Z.; Chuaqui, C.; Singh, J. Structural interaction fingerprint (SIFt): a novel method for analyzing three-dimensional protein-ligand binding interactions J. Med. Chem. 2004, 47, 337-344 10.1021/jm030331x
-
(2004)
J. Med. Chem.
, vol.47
, pp. 337-344
-
-
Deng, Z.1
Chuaqui, C.2
Singh, J.3
-
119
-
-
84864343828
-
A designed ankyrin repeat protein selected to bind to tubulin caps the microtubule plus end
-
Pecqueur, L.; Duellberg, C.; Dreier, B.; Jiang, Q.; Wang, C.; Plueckthun, A.; Surrey, T.; Gigant, B.; Knossow, M. A designed ankyrin repeat protein selected to bind to tubulin caps the microtubule plus end Proc. Natl. Acad. Sci. U. S. A. 2012, 109, 12011-12016 10.1073/pnas.1204129109
-
(2012)
Proc. Natl. Acad. Sci. U. S. A.
, vol.109
, pp. 12011-12016
-
-
Pecqueur, L.1
Duellberg, C.2
Dreier, B.3
Jiang, Q.4
Wang, C.5
Plueckthun, A.6
Surrey, T.7
Gigant, B.8
Knossow, M.9
-
120
-
-
84865074275
-
A TOG:alpha beta-tubulin complex structure reveals conformation-based mechanisms for a microtubule polymerase
-
Ayaz, P.; Ye, X.; Huddleston, P.; Brautigam, C. A.; Rice, L. M. A TOG:alpha beta-tubulin complex structure reveals conformation-based mechanisms for a microtubule polymerase Science 2012, 337, 857-860 10.1126/science.1221698
-
(2012)
Science
, vol.337
, pp. 857-860
-
-
Ayaz, P.1
Ye, X.2
Huddleston, P.3
Brautigam, C.A.4
Rice, L.M.5
-
121
-
-
0026558326
-
Mechanism of inhibition of microtubule polymerization by colchicine - Inhibitory potencies of unliganded colchicine and tubulin colchicine complexes
-
Skoufias, D. A.; Wilson, L. Mechanism of inhibition of microtubule polymerization by colchicine-inhibitory potencies of unliganded colchicine and tubulin colchicine complexes Biochemistry 1992, 31, 738-746 10.1021/bi00118a015
-
(1992)
Biochemistry
, vol.31
, pp. 738-746
-
-
Skoufias, D.A.1
Wilson, L.2
-
122
-
-
84948115174
-
Control of microtubule organization and dynamics: Two ends in the limelight
-
Akhmanova, A.; Steinmetz, M. O. Control of microtubule organization and dynamics: two ends in the limelight Nat. Rev. Mol. Cell Biol. 2015, 16, 711-726 10.1038/nrm4084
-
(2015)
Nat. Rev. Mol. Cell Biol.
, vol.16
, pp. 711-726
-
-
Akhmanova, A.1
Steinmetz, M.O.2
-
123
-
-
84876006690
-
Synthesis and biochemical activities of antiproliferative amino acid and phosphate derivatives of microtubule-disrupting β-lactam combretastatins
-
O'Boyle, N. M.; Greene, L. M.; Keely, N. O.; Wang, S.; Cotter, T. S.; Zisterer, D. M.; Meegan, M. J. Synthesis and biochemical activities of antiproliferative amino acid and phosphate derivatives of microtubule-disrupting β-lactam combretastatins Eur. J. Med. Chem. 2013, 62, 705-721 10.1016/j.ejmech.2013.01.016
-
(2013)
Eur. J. Med. Chem.
, vol.62
, pp. 705-721
-
-
O'Boyle, N.M.1
Greene, L.M.2
Keely, N.O.3
Wang, S.4
Cotter, T.S.5
Zisterer, D.M.6
Meegan, M.J.7
-
124
-
-
84875233542
-
Metabolic fate of combretastatin A-1: LC-DAD-MS/MS investigation and biological evaluation of its reactive metabolites
-
Aprile, S.; Zaninetti, R.; Del Grosso, E.; Genazzani, A. A.; Grosa, G. Metabolic fate of combretastatin A-1: LC-DAD-MS/MS investigation and biological evaluation of its reactive metabolites J. Pharm. Biomed. Anal. 2013, 78-79, 233-242 10.1016/j.jpba.2013.02.030
-
(2013)
J. Pharm. Biomed. Anal.
, vol.7879
, pp. 233-242
-
-
Aprile, S.1
Zaninetti, R.2
Del Grosso, E.3
Genazzani, A.A.4
Grosa, G.5
-
125
-
-
40149088986
-
Prodrugs: Design and clinical applications
-
Rautio, J.; Kumpulainen, H.; Heimbach, T.; Oliyai, R.; Oh, D.; Jarvinen, T.; Savolainen, J. Prodrugs: design and clinical applications Nat. Rev. Drug Discovery 2008, 7, 255-270 10.1038/nrd2468
-
(2008)
Nat. Rev. Drug Discovery
, vol.7
, pp. 255-270
-
-
Rautio, J.1
Kumpulainen, H.2
Heimbach, T.3
Oliyai, R.4
Oh, D.5
Jarvinen, T.6
Savolainen, J.7
-
126
-
-
84899956978
-
A phase i pharmacokinetic study of the vascular disrupting agent ombrabulin (AVE8062) and docetaxel in advanced solid tumours
-
Eskens, F. A. L. M.; Tresca, P.; Tosi, D.; Van Doorn, L.; Fontaine, H.; Van der Gaast, A.; Veyrat-Follet, C.; Oprea, C.; Hospitel, M.; Dieras, V. A phase I pharmacokinetic study of the vascular disrupting agent ombrabulin (AVE8062) and docetaxel in advanced solid tumours Br. J. Cancer 2014, 110, 2170-2177 10.1038/bjc.2014.137
-
(2014)
Br. J. Cancer
, vol.110
, pp. 2170-2177
-
-
Eskens, F.A.L.M.1
Tresca, P.2
Tosi, D.3
Van Doorn, L.4
Fontaine, H.5
Van Der Gaast, A.6
Veyrat-Follet, C.7
Oprea, C.8
Hospitel, M.9
Dieras, V.10
-
127
-
-
84918533922
-
Folate receptor-mediated enhanced and specific delivery of far-red light-activatable prodrugs of combretastatin A-4 to FR-positive tumor
-
Nkepang, G.; Bio, M.; Rajaputra, P.; Awuah, S. G.; You, Y. Folate receptor-mediated enhanced and specific delivery of far-red light-activatable prodrugs of combretastatin A-4 to FR-positive tumor Bioconjugate Chem. 2014, 25, 2175-2188 10.1021/bc500376j
-
(2014)
Bioconjugate Chem.
, vol.25
, pp. 2175-2188
-
-
Nkepang, G.1
Bio, M.2
Rajaputra, P.3
Awuah, S.G.4
You, Y.5
-
128
-
-
84855312255
-
Targeted delivery of a combination therapy consisting of combretastatin A4 and low-dose doxorubicin against tumor neovasculature
-
Yang, T.; Wang, Y.; Li, Z.; Dai, W.; Yin, J.; Liang, L.; Ying, X.; Zhou, S.; Wang, J.; Zhang, X.; Zhang, Q. Targeted delivery of a combination therapy consisting of combretastatin A4 and low-dose doxorubicin against tumor neovasculature Nanomedicine 2012, 8, 81-92 10.1016/j.nano.2011.05.003
-
(2012)
Nanomedicine
, vol.8
, pp. 81-92
-
-
Yang, T.1
Wang, Y.2
Li, Z.3
Dai, W.4
Yin, J.5
Liang, L.6
Ying, X.7
Zhou, S.8
Wang, J.9
Zhang, X.10
Zhang, Q.11
-
129
-
-
77649185057
-
Targeted delivery of RGD-modified liposomes encapsulating both combretastatin A-4 and doxorubicin for tumor therapy: In vitro and in vivo studies
-
Zhang, Y.; Wang, J.; Bian, D.; Zhang, X.; Zhang, Q. Targeted delivery of RGD-modified liposomes encapsulating both combretastatin A-4 and doxorubicin for tumor therapy: In vitro and in vivo studies Eur. J. Pharm. Biopharm. 2010, 74, 467-473 10.1016/j.ejpb.2010.01.002
-
(2010)
Eur. J. Pharm. Biopharm.
, vol.74
, pp. 467-473
-
-
Zhang, Y.1
Wang, J.2
Bian, D.3
Zhang, X.4
Zhang, Q.5
-
130
-
-
84863913286
-
Multifunctional dendrimer/combretastatin A4 inclusion complexes enable in vitro targeted cancer therapy
-
Zhang, M.; Guo, R.; Wang, Y.; Cao, X.; Shen, M.; Shi, X. Multifunctional dendrimer/combretastatin A4 inclusion complexes enable in vitro targeted cancer therapy Int. J. Nanomed. 2011, 6, 2337-2349 10.2147/IJN.S24705
-
(2011)
Int. J. Nanomed.
, vol.6
, pp. 2337-2349
-
-
Zhang, M.1
Guo, R.2
Wang, Y.3
Cao, X.4
Shen, M.5
Shi, X.6
-
131
-
-
84879600243
-
PH-sensitive pullulan-based nanoparticle carrier of methotrexate and combretastatin A4 for the combination therapy against hepatocellular carcinoma
-
Wang, Y.; Chen, H.; Liu, Y.; Wu, J.; Zhou, P.; Wang, Y.; Li, R.; Yang, X.; Zhang, N. pH-sensitive pullulan-based nanoparticle carrier of methotrexate and combretastatin A4 for the combination therapy against hepatocellular carcinoma Biomaterials 2013, 34, 7181-7190 10.1016/j.biomaterials.2013.05.081
-
(2013)
Biomaterials
, vol.34
, pp. 7181-7190
-
-
Wang, Y.1
Chen, H.2
Liu, Y.3
Wu, J.4
Zhou, P.5
Wang, Y.6
Li, R.7
Yang, X.8
Zhang, N.9
-
132
-
-
23144456813
-
Temporal targeting of tumour cells and neovasculature with a nanoscale delivery system
-
Sengupta, S.; Eavarone, D.; Capila, I.; Zhao, G.; Watson, N.; Kiziltepe, T.; Sasisekharan, R. Temporal targeting of tumour cells and neovasculature with a nanoscale delivery system Nature 2005, 436, 568-572 10.1038/nature03794
-
(2005)
Nature
, vol.436
, pp. 568-572
-
-
Sengupta, S.1
Eavarone, D.2
Capila, I.3
Zhao, G.4
Watson, N.5
Kiziltepe, T.6
Sasisekharan, R.7
-
133
-
-
84946426670
-
A chimeric cetuximab-functionalized corona as a potent delivery system for microtubule-destabilizing nanocomplexes to hepatocellular carcinoma cells: A focus on EGFR and tubulin intracellular dynamics
-
Poojari, R.; Kini, S.; Srivastava, R.; Panda, D. A chimeric cetuximab-functionalized corona as a potent delivery system for microtubule-destabilizing nanocomplexes to hepatocellular carcinoma cells: a focus on EGFR and tubulin intracellular dynamics Mol. Pharmaceutics 2015, 12, 3908-3923 10.1021/acs.molpharmaceut.5b00337
-
(2015)
Mol. Pharmaceutics
, vol.12
, pp. 3908-3923
-
-
Poojari, R.1
Kini, S.2
Srivastava, R.3
Panda, D.4
-
134
-
-
84939267405
-
Coadministration of vascular disrupting agents and nanomedicines to eradicate tumors from peripheral and central regions
-
Song, W.; Tang, Z.; Zhang, D.; Yu, H.; Chen, X. Coadministration of vascular disrupting agents and nanomedicines to eradicate tumors from peripheral and central regions Small 2015, 11, 3755-3761 10.1002/smll.201500324
-
(2015)
Small
, vol.11
, pp. 3755-3761
-
-
Song, W.1
Tang, Z.2
Zhang, D.3
Yu, H.4
Chen, X.5
-
135
-
-
84947494942
-
Pharmacokinetic strategies to improve drug penetration and entrapment within solid tumors
-
Al-Abd, A. M.; Aljehani, Z. K.; Gazzaz, R. W.; Fakhri, S. H.; Jabbad, A. H.; Alahdal, A. M.; Torchilin, V. P. Pharmacokinetic strategies to improve drug penetration and entrapment within solid tumors J. Controlled Release 2015, 219, 269-277 10.1016/j.jconrel.2015.08.055
-
(2015)
J. Controlled Release
, vol.219
, pp. 269-277
-
-
Al-Abd, A.M.1
Aljehani, Z.K.2
Gazzaz, R.W.3
Fakhri, S.H.4
Jabbad, A.H.5
Alahdal, A.M.6
Torchilin, V.P.7
-
136
-
-
0035417875
-
Mechanisms associated with tumor vascular shut-down induced by combretastatin A-4 phosphate: Intravital microscopy and measurement of vascular permeability
-
Tozer, G. M.; Prise, V. E.; Wilso, J.; Cemazar, M.; Shan, S.; Dewhirst, M. W.; Barber, P. R.; Vojnovic, B.; Chaplin, D. J. Mechanisms associated with tumor vascular shut-down induced by combretastatin A-4 phosphate: Intravital microscopy and measurement of vascular permeability Cancer Res. 2001, 61, 6413-6422
-
(2001)
Cancer Res.
, vol.61
, pp. 6413-6422
-
-
Tozer, G.M.1
Prise, V.E.2
Wilso, J.3
Cemazar, M.4
Shan, S.5
Dewhirst, M.W.6
Barber, P.R.7
Vojnovic, B.8
Chaplin, D.J.9
-
137
-
-
35448952260
-
Assessment of tumor response to the vascular disrupting agents 5,6-dimethylxanthenone-4-acetic acid or combretastatin-A4-phosphate by intrinsic susceptibility magnetic resonance imaging
-
McPhail, L. D.; Griffiths, J. R.; Robinson, S. P. Assessment of tumor response to the vascular disrupting agents 5,6-dimethylxanthenone-4-acetic acid or combretastatin-A4-phosphate by intrinsic susceptibility magnetic resonance imaging Int. J. Radiat. Oncol., Biol., Phys. 2007, 69, 1238-1245 10.1016/j.ijrobp.2007.08.025
-
(2007)
Int. J. Radiat. Oncol., Biol., Phys.
, vol.69
, pp. 1238-1245
-
-
McPhail, L.D.1
Griffiths, J.R.2
Robinson, S.P.3
-
138
-
-
51149108751
-
The effect of combretastatin A4 disodium phosphate and 5,6- dimethylxanthenone-4-acetic acid on water diffusion and blood perfusion in tumours
-
Chen, G.; Horsman, M. R.; Pedersen, M.; Pang, Q.; Stødkilde-Jørgensen, H. The effect of combretastatin A4 disodium phosphate and 5,6- dimethylxanthenone-4-acetic acid on water diffusion and blood perfusion in tumours Acta Oncol. 2008, 47, 1071-1076 10.1080/02841860701769750
-
(2008)
Acta Oncol.
, vol.47
, pp. 1071-1076
-
-
Chen, G.1
Horsman, M.R.2
Pedersen, M.3
Pang, Q.4
Stødkilde-Jørgensen, H.5
-
139
-
-
46749103224
-
Antivascular effects of combretastatin A4 phosphate in breast cancer xenograft assessed using dynamic bioluminescence imaging and confirmed by MRI
-
Zhao, D.; Richer, E.; Antich, P. P.; Mason, R. P. Antivascular effects of combretastatin A4 phosphate in breast cancer xenograft assessed using dynamic bioluminescence imaging and confirmed by MRI FASEB J. 2008, 22, 2445-2451 10.1096/fj.07-103713
-
(2008)
FASEB J.
, vol.22
, pp. 2445-2451
-
-
Zhao, D.1
Richer, E.2
Antich, P.P.3
Mason, R.P.4
-
140
-
-
84870332928
-
Combretastatin A-4 phosphate affects tumor vessel volume and size distribution as assessed using MRI-based vessel size imaging
-
Nielsen, T.; Bentzen, L.; Pedersen, M.; Tramm, T.; Rijken, P. F. J. W.; Bussink, J.; Horsman, M. R.; Ostergaard, L. Combretastatin A-4 phosphate affects tumor vessel volume and size distribution as assessed using MRI-based vessel size imaging Clin. Cancer Res. 2012, 18, 6469-6477 10.1158/1078-0432.CCR-12-2014
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 6469-6477
-
-
Nielsen, T.1
Bentzen, L.2
Pedersen, M.3
Tramm, T.4
Rijken, P.F.J.W.5
Bussink, J.6
Horsman, M.R.7
Ostergaard, L.8
-
141
-
-
0034472914
-
Combretastatins novel vascular targeting drugs for improving anti-cancer therapy: Combretastatins and conventional therapy
-
Horsman, M. R.; Murata, R.; Breidahl, T.; Nielsen, F. U.; Maxwell, R. J.; Stødkiled-Jørgensen, H.; Overgaard, J. Combretastatins novel vascular targeting drugs for improving anti-cancer therapy: Combretastatins and conventional therapy Adv. Exp. Med. Biol. 2000, 476, 311-323 10.1007/978-1-4615-4221-6-26
-
(2000)
Adv. Exp. Med. Biol.
, vol.476
, pp. 311-323
-
-
Horsman, M.R.1
Murata, R.2
Breidahl, T.3
Nielsen, F.U.4
Maxwell, R.J.5
Stødkiled-Jørgensen, H.6
Overgaard, J.7
-
142
-
-
80052026194
-
Vascular effects dominate solid tumor response to treatment with combretastatin A-4-phosphate
-
Lunt, S. J.; Akerman, S.; Hill, S. A.; Fisher, M.; Wright, V. J.; Reyes-Aldasoro, C. C.; Tozer, G. M.; Kanthou, C. Vascular effects dominate solid tumor response to treatment with combretastatin A-4-phosphate Int. J. Cancer 2011, 129, 1979-1989 10.1002/ijc.25848
-
(2011)
Int. J. Cancer
, vol.129
, pp. 1979-1989
-
-
Lunt, S.J.1
Akerman, S.2
Hill, S.A.3
Fisher, M.4
Wright, V.J.5
Reyes-Aldasoro, C.C.6
Tozer, G.M.7
Kanthou, C.8
-
143
-
-
33847322988
-
Early effects of combretastatin-A4 disodium phosphate on tumor perfusion and interstitial fluid pressure
-
Ley, C. D.; Horsman, M. R.; Kristjansen, P. E. G. Early effects of combretastatin-A4 disodium phosphate on tumor perfusion and interstitial fluid pressure Neoplasia 2007, 9, 108-112 10.1593/neo.06733
-
(2007)
Neoplasia
, vol.9
, pp. 108-112
-
-
Ley, C.D.1
Horsman, M.R.2
Kristjansen, P.E.G.3
-
144
-
-
84919371931
-
An in vivo role for Rho kinase activation in the tumour vascular disrupting activity of combretastatin A-4 3-O-phosphate
-
Williams, L. J.; Mukherjee, D.; Fisher, M.; Reyes-Aldasoro, C. C.; Akerman, S.; Kanthou, C.; Tozer, G. M. An in vivo role for Rho kinase activation in the tumour vascular disrupting activity of combretastatin A-4 3-O-phosphate Br. J. Pharmacol. 2014, 171, 4902-4913 10.1111/bph.12817
-
(2014)
Br. J. Pharmacol.
, vol.171
, pp. 4902-4913
-
-
Williams, L.J.1
Mukherjee, D.2
Fisher, M.3
Reyes-Aldasoro, C.C.4
Akerman, S.5
Kanthou, C.6
Tozer, G.M.7
-
145
-
-
27644466314
-
Combretastatin A4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-cadherin signaling
-
Vincent, L.; Kermani, P.; Young, L. M.; Cheng, J.; Zhang, F.; Shido, K.; Lam, G.; Bompais-Vincent, H.; Zhu, Z.; Hicklin, D. J.; Bohlen, P.; Chaplin, D. J.; May, C.; Rafii, S. Combretastatin A4 phosphate induces rapid regression of tumor neovessels and growth through interference with vascular endothelial-cadherin signaling J. Clin. Invest. 2005, 115, 2992-3006 10.1172/JCI24586
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 2992-3006
-
-
Vincent, L.1
Kermani, P.2
Young, L.M.3
Cheng, J.4
Zhang, F.5
Shido, K.6
Lam, G.7
Bompais-Vincent, H.8
Zhu, Z.9
Hicklin, D.J.10
Bohlen, P.11
Chaplin, D.J.12
May, C.13
Rafii, S.14
-
146
-
-
84860250385
-
The vascular-disrupting agent combretastatin impairs splitting and sprouting forms of physiological angiogenesis
-
Hussain, A.; Steimle, M.; Hoppeler, H.; Baum, O.; Egginton, S. The vascular-disrupting agent combretastatin impairs splitting and sprouting forms of physiological angiogenesis Microcirculation 2012, 19, 296-305 10.1111/j.1549-8719.2012.00160.x
-
(2012)
Microcirculation
, vol.19
, pp. 296-305
-
-
Hussain, A.1
Steimle, M.2
Hoppeler, H.3
Baum, O.4
Egginton, S.5
-
147
-
-
84884884580
-
Deoxypodophyllotoxin exerts both anti-angiogenic and vascular disrupting effects
-
Jiang, Z.; Wu, M.; Miao, J.; Duan, H.; Zhang, S.; Chen, M.; Sun, L.; Wang, Y.; Zhang, X.; Zhu, X.; Zhang, L. Deoxypodophyllotoxin exerts both anti-angiogenic and vascular disrupting effects Int. J. Biochem. Cell Biol. 2013, 45, 1710-1719 10.1016/j.biocel.2013.04.030
-
(2013)
Int. J. Biochem. Cell Biol.
, vol.45
, pp. 1710-1719
-
-
Jiang, Z.1
Wu, M.2
Miao, J.3
Duan, H.4
Zhang, S.5
Chen, M.6
Sun, L.7
Wang, Y.8
Zhang, X.9
Zhu, X.10
Zhang, L.11
-
148
-
-
0037457666
-
Vascular targeting effect of combretastatin A-4 phosphate dominates the inherent angiogenesis inhibitory activity
-
Ahmed, B.; Van Eijk, L. I.; Bouma-ter Steege, J. C. A.; Van Der Schaft, D. W. J.; Van Esch, A. M.; Joosten-Achjanie, S. R.; Lambin, P.; Landuyt, W.; Griffioen, A. W. Vascular targeting effect of combretastatin A-4 phosphate dominates the inherent angiogenesis inhibitory activity Int. J. Cancer 2003, 105, 20-25 10.1002/ijc.11010
-
(2003)
Int. J. Cancer
, vol.105
, pp. 20-25
-
-
Ahmed, B.1
Van Eijk, L.I.2
Bouma-Ter Steege, J.C.A.3
Van Der Schaft, D.W.J.4
Van Esch, A.M.5
Joosten-Achjanie, S.R.6
Lambin, P.7
Landuyt, W.8
Griffioen, A.W.9
-
149
-
-
84879209616
-
TR-644 a novel potent tubulin binding agent induces impairment of endothelial cells function and inhibits angiogenesis
-
Porcù, E.; Viola, G.; Bortolozzi, R.; Persano, L.; Mitola, S.; Ronca, R.; Presta, M.; Romagnoli, R.; Baraldi, P. G.; Basso, G. TR-644 a novel potent tubulin binding agent induces impairment of endothelial cells function and inhibits angiogenesis Angiogenesis 2013, 16, 647-662 10.1007/s10456-013-9343-z
-
(2013)
Angiogenesis
, vol.16
, pp. 647-662
-
-
Porcù, E.1
Viola, G.2
Bortolozzi, R.3
Persano, L.4
Mitola, S.5
Ronca, R.6
Presta, M.7
Romagnoli, R.8
Baraldi, P.G.9
Basso, G.10
-
150
-
-
61349094787
-
Up-regulation of connective tissue growth factor in endothelial cells by the microtubule-destabilizing agent combretastatin A-4
-
Samarin, J.; Rehm, M.; Krueger, B.; Waschke, J.; Goppelt-Struebe, M. Up-regulation of connective tissue growth factor in endothelial cells by the microtubule-destabilizing agent combretastatin A-4 Mol. Cancer Res. 2009, 7, 180-188 10.1158/1541-7786.MCR-08-0292
-
(2009)
Mol. Cancer Res.
, vol.7
, pp. 180-188
-
-
Samarin, J.1
Rehm, M.2
Krueger, B.3
Waschke, J.4
Goppelt-Struebe, M.5
-
151
-
-
84888863628
-
Stilbene 5c, a microtubule poison with vascular disrupting properties that induces multiple modes of growth arrest and cell death
-
Alotaibi, M. R.; Asnake, B.; Di, X.; Beckman, M. J.; Durrant, D.; Simoni, D.; Baruchello, R.; Lee, R. M.; Schwartz, E. L.; Gewirtz, D. A. Stilbene 5c, a microtubule poison with vascular disrupting properties that induces multiple modes of growth arrest and cell death Biochem. Pharmacol. 2013, 86, 1688-1698 10.1016/j.bcp.2013.10.007
-
(2013)
Biochem. Pharmacol.
, vol.86
, pp. 1688-1698
-
-
Alotaibi, M.R.1
Asnake, B.2
Di, X.3
Beckman, M.J.4
Durrant, D.5
Simoni, D.6
Baruchello, R.7
Lee, R.M.8
Schwartz, E.L.9
Gewirtz, D.A.10
-
152
-
-
77954882234
-
Combretastatin A-4 inhibits cell growth and metastasis in bladder cancer cells and retards tumour growth in a murine orthotopic bladder tumour model
-
Shen, C. H.; Shee, J. J.; Wu, J. Y.; Lin, Y. W.; Wu, J. D.; Liu, Y. W. Combretastatin A-4 inhibits cell growth and metastasis in bladder cancer cells and retards tumour growth in a murine orthotopic bladder tumour model Br. J. Pharmacol. 2010, 160, 2008-2027 10.1111/j.1476-5381.2010.00861.x
-
(2010)
Br. J. Pharmacol.
, vol.160
, pp. 2008-2027
-
-
Shen, C.H.1
Shee, J.J.2
Wu, J.Y.3
Lin, Y.W.4
Wu, J.D.5
Liu, Y.W.6
-
153
-
-
4644316617
-
The tubulin-binding agent combretastatin A-4-phosphate arrests endothelial cells in mitosis and induces mitotic cell death
-
Kanthou, C.; Greco, O.; Stratford, A.; Cook, I.; Knight, R.; Benzakour, O.; Tozer, G. The tubulin-binding agent combretastatin A-4-phosphate arrests endothelial cells in mitosis and induces mitotic cell death Am. J. Pathol. 2004, 165, 1401-1411 10.1016/S0002-9440(10)63398-6
-
(2004)
Am. J. Pathol.
, vol.165
, pp. 1401-1411
-
-
Kanthou, C.1
Greco, O.2
Stratford, A.3
Cook, I.4
Knight, R.5
Benzakour, O.6
Tozer, G.7
-
154
-
-
0036023440
-
Combretastatin-A4 prodrug induces mitotic catastrophe in chronic lymphocytic leukemia cell line independent of caspase activation and poly(ADP-ribose) polymerase cleavage
-
Nabha, S. M.; Mohammad, R. M.; Dandashi, M. H.; Coupaye-Gerard, B.; Aboukameel, A.; Pettit, G. R.; Al-Katib, A. M. Combretastatin-A4 prodrug induces mitotic catastrophe in chronic lymphocytic leukemia cell line independent of caspase activation and poly(ADP-ribose) polymerase cleavage Clin. Cancer Res. 2002, 8, 2735-2741
-
(2002)
Clin. Cancer Res.
, vol.8
, pp. 2735-2741
-
-
Nabha, S.M.1
Mohammad, R.M.2
Dandashi, M.H.3
Coupaye-Gerard, B.4
Aboukameel, A.5
Pettit, G.R.6
Al-Katib, A.M.7
-
155
-
-
79960957085
-
Mitotic catastrophe: A mechanism for avoiding genomic instability
-
Vitale, I.; Galluzzi, L.; Castedo, M.; Kroemer, G. Mitotic catastrophe: a mechanism for avoiding genomic instability Nat. Rev. Mol. Cell Biol. 2011, 12, 385-392 10.1038/nrm3115
-
(2011)
Nat. Rev. Mol. Cell Biol.
, vol.12
, pp. 385-392
-
-
Vitale, I.1
Galluzzi, L.2
Castedo, M.3
Kroemer, G.4
-
156
-
-
0033941680
-
Effects of Combretastatin A-4 prodrug against a panel of malignant human B-lymphoid cell lines
-
Nabha, S. M.; Wall, N. R.; Mohammad, R. M.; Pettit, G. R.; Al-Katib, A. M. Effects of Combretastatin A-4 prodrug against a panel of malignant human B-lymphoid cell lines Anti-Cancer Drugs 2000, 11, 385-392 10.1097/00001813-200006000-00009
-
(2000)
Anti-Cancer Drugs
, vol.11
, pp. 385-392
-
-
Nabha, S.M.1
Wall, N.R.2
Mohammad, R.M.3
Pettit, G.R.4
Al-Katib, A.M.5
-
157
-
-
42149153777
-
The tubulin-depolymerising agent combretastatin-4 induces ectopic aster assembly and mitotic catastrophe in lung cancer cells H460
-
Cenciarelli, C.; Tanzarella, C.; Vitale, I.; Pisano, C.; Crateri, P.; Meschini, S.; Arancia, G.; Antoccia, A. The tubulin-depolymerising agent combretastatin-4 induces ectopic aster assembly and mitotic catastrophe in lung cancer cells H460 Apoptosis 2008, 13, 659-669 10.1007/s10495-008-0200-2
-
(2008)
Apoptosis
, vol.13
, pp. 659-669
-
-
Cenciarelli, C.1
Tanzarella, C.2
Vitale, I.3
Pisano, C.4
Crateri, P.5
Meschini, S.6
Arancia, G.7
Antoccia, A.8
-
158
-
-
33845758418
-
Combretastatin CA-4 and combretastatin derivative induce mitotic catastrophe dependent on spindle checkpoint and caspase-3 activation in non-small cell lung cancer cells
-
Vitale, I.; Antoccia, A.; Cenciarelli, C.; Crateri, P.; Meschini, S.; Arancia, G.; Pisano, C.; Tanzarella, C. Combretastatin CA-4 and combretastatin derivative induce mitotic catastrophe dependent on spindle checkpoint and caspase-3 activation in non-small cell lung cancer cells Apoptosis 2007, 12, 155-166 10.1007/s10495-006-0491-0
-
(2007)
Apoptosis
, vol.12
, pp. 155-166
-
-
Vitale, I.1
Antoccia, A.2
Cenciarelli, C.3
Crateri, P.4
Meschini, S.5
Arancia, G.6
Pisano, C.7
Tanzarella, C.8
-
159
-
-
80052949837
-
Synthesis, biochemical and molecular modelling studies of antiproliferative azetidinones causing microtubule disruption and mitotic catastrophe
-
O'Boyle, N. M.; Carr, M.; Greene, L. M.; Keely, N. O.; Knox, A. J. S.; McCabe, T.; Lloyd, D. G.; Zisterer, D. M.; Meegan, M. J. Synthesis, biochemical and molecular modelling studies of antiproliferative azetidinones causing microtubule disruption and mitotic catastrophe Eur. J. Med. Chem. 2011, 46, 4595-4607 10.1016/j.ejmech.2011.07.039
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 4595-4607
-
-
O'Boyle, N.M.1
Carr, M.2
Greene, L.M.3
Keely, N.O.4
Knox, A.J.S.5
McCabe, T.6
Lloyd, D.G.7
Zisterer, D.M.8
Meegan, M.J.9
-
161
-
-
0032532391
-
Induction of apoptosis in proliferating human endothelial cells by the tumor-specific antiangiogenesis agent combretastatin A-4
-
Iyer, S.; Chaplin, D. J.; Rosenthal, D. S.; Boulares, A. H.; Li, L. Y.; Smulson, M. E. Induction of apoptosis in proliferating human endothelial cells by the tumor-specific antiangiogenesis agent combretastatin A-4 Cancer Res. 1998, 58, 4510-4514
-
(1998)
Cancer Res.
, vol.58
, pp. 4510-4514
-
-
Iyer, S.1
Chaplin, D.J.2
Rosenthal, D.S.3
Boulares, A.H.4
Li, L.Y.5
Smulson, M.E.6
-
162
-
-
41349118110
-
The microtubule-targeting agent CA4P regresses leukemic xenografts by disrupting interaction with vascular cells and mitochondrial-dependent cell death
-
Petit, I.; Karajannis, M. A.; Vincent, L.; Young, L.; Butler, J.; Hooper, A. T.; Shido, K.; Steller, H.; Chaplin, D. J.; Feldman, E.; Rafii, S. The microtubule-targeting agent CA4P regresses leukemic xenografts by disrupting interaction with vascular cells and mitochondrial-dependent cell death Blood 2008, 111, 1951-1961 10.1182/blood-2007-05-089219
-
(2008)
Blood
, vol.111
, pp. 1951-1961
-
-
Petit, I.1
Karajannis, M.A.2
Vincent, L.3
Young, L.4
Butler, J.5
Hooper, A.T.6
Shido, K.7
Steller, H.8
Chaplin, D.J.9
Feldman, E.10
Rafii, S.11
-
163
-
-
80052508953
-
Role of Bim in apoptosis induced in H460 lung tumor cells by the spindle poison combretastatin-A4
-
Mendez, G.; Policarpi, C.; Cenciarelli, C.; Tanzarella, C.; Antoccia, A. Role of Bim in apoptosis induced in H460 lung tumor cells by the spindle poison combretastatin-A4 Apoptosis 2011, 16, 940-949 10.1007/s10495-011-0619-8
-
(2011)
Apoptosis
, vol.16
, pp. 940-949
-
-
Mendez, G.1
Policarpi, C.2
Cenciarelli, C.3
Tanzarella, C.4
Antoccia, A.5
-
164
-
-
84896314503
-
Combretastatin A-4 induces p53 mitochondrial-relocalisation independent-apoptosis in non-small lung cancer cells
-
Méndez-Callejas, G. M.; Leone, S.; Tanzarella, C.; Antoccia, A. Combretastatin A-4 induces p53 mitochondrial-relocalisation independent-apoptosis in non-small lung cancer cells Cell Biol. Int. 2014, 38, 296-308 10.1002/cbin.10199
-
(2014)
Cell Biol. Int.
, vol.38
, pp. 296-308
-
-
Méndez-Callejas, G.M.1
Leone, S.2
Tanzarella, C.3
Antoccia, A.4
-
165
-
-
84947612647
-
Role of JNK and NF-κB in mediating the effect of combretastatin A-4 and brimamin on endothelial and carcinoma cells
-
Mahal, K.; Ahmad, A.; Sethi, S.; Resch, M.; Ficner, R.; Sarkar, F. H.; Schobert, R.; Biersack, B. Role of JNK and NF-κB in mediating the effect of combretastatin A-4 and brimamin on endothelial and carcinoma cells Cell. Oncol. 2015, 38, 463-478 10.1007/s13402-015-0243-7
-
(2015)
Cell. Oncol.
, vol.38
, pp. 463-478
-
-
Mahal, K.1
Ahmad, A.2
Sethi, S.3
Resch, M.4
Ficner, R.5
Sarkar, F.H.6
Schobert, R.7
Biersack, B.8
-
166
-
-
34548837788
-
Combretastatin A4-induced differential cytotoxicity and reduced metastatic ability by inhibition of AKT function in human gastric cancer cells
-
Lin, H. L.; Chiou, S. H.; Wu, C. W.; Lin, W. B.; Chen, L. H.; Yang, Y. P.; Tsai, M. L.; Uen, Y. H.; Liou, J. P.; Chi, C. W. Combretastatin A4-induced differential cytotoxicity and reduced metastatic ability by inhibition of AKT function in human gastric cancer cells J. Pharmacol. Exp. Ther. 2007, 323, 365-373 10.1124/jpet.107.124966
-
(2007)
J. Pharmacol. Exp. Ther.
, vol.323
, pp. 365-373
-
-
Lin, H.L.1
Chiou, S.H.2
Wu, C.W.3
Lin, W.B.4
Chen, L.H.5
Yang, Y.P.6
Tsai, M.L.7
Uen, Y.H.8
Liou, J.P.9
Chi, C.W.10
-
167
-
-
84912535573
-
Combretastatin (CA)-4 and its novel analogue CA-432 impair T-cell migration through the Rho/ROCK signalling pathway
-
Pollock, J. K.; Verma, N. K.; O'Boyle, N. M.; Carr, M.; Meegan, M. J.; Zisterer, D. M. Combretastatin (CA)-4 and its novel analogue CA-432 impair T-cell migration through the Rho/ROCK signalling pathway Biochem. Pharmacol. 2014, 92, 544-557 10.1016/j.bcp.2014.10.002
-
(2014)
Biochem. Pharmacol.
, vol.92
, pp. 544-557
-
-
Pollock, J.K.1
Verma, N.K.2
O'Boyle, N.M.3
Carr, M.4
Meegan, M.J.5
Zisterer, D.M.6
-
168
-
-
0037141466
-
A novel combretastatin A-4 derivative, AC7700, strongly stanches tumour blood flow and inhibits growth of tumours developing in various tissues and organs
-
Hori, K.; Saito, S.; Kubota, K. A novel combretastatin A-4 derivative, AC7700, strongly stanches tumour blood flow and inhibits growth of tumours developing in various tissues and organs Br. J. Cancer 2002, 86, 1604-1614 10.1038/sj.bjc.6600296
-
(2002)
Br. J. Cancer
, vol.86
, pp. 1604-1614
-
-
Hori, K.1
Saito, S.2
Kubota, K.3
-
169
-
-
84941283246
-
Rho GTPase signalling in cell migration
-
Ridley, A. J. Rho GTPase signalling in cell migration Curr. Opin. Cell Biol. 2015, 36, 103-112 10.1016/j.ceb.2015.08.005
-
(2015)
Curr. Opin. Cell Biol.
, vol.36
, pp. 103-112
-
-
Ridley, A.J.1
-
170
-
-
0037085753
-
The tumor vascular targeting agent combretastatin A-4-phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells
-
Kanthou, C.; Tozer, G. M. The tumor vascular targeting agent combretastatin A-4-phosphate induces reorganization of the actin cytoskeleton and early membrane blebbing in human endothelial cells Blood 2002, 99, 2060-2069 10.1182/blood.V99.6.2060
-
(2002)
Blood
, vol.99
, pp. 2060-2069
-
-
Kanthou, C.1
Tozer, G.M.2
-
171
-
-
84945151355
-
Deoxypodophyllotoxin suppresses tumor vasculature in HUVECs by promoting cytoskeleton remodeling through LKB1-AMPK dependent Rho A activation
-
Wang, Y.; Wang, B.; Guerram, M.; Sun, L.; Shi, W.; Tian, C.; Zhu, X.; Jiang, Z.; Zhang, L. Deoxypodophyllotoxin suppresses tumor vasculature in HUVECs by promoting cytoskeleton remodeling through LKB1-AMPK dependent Rho A activation Oncotarget 2015, 6, 29497-29512 10.18632/oncotarget.4985
-
(2015)
Oncotarget
, vol.6
, pp. 29497-29512
-
-
Wang, Y.1
Wang, B.2
Guerram, M.3
Sun, L.4
Shi, W.5
Tian, C.6
Zhu, X.7
Jiang, Z.8
Zhang, L.9
-
172
-
-
84909997138
-
Prevention of cancer recurrence in tumor margins by stopping microcirculation in the tumor and tumor-host interface
-
Hori, K.; Akita, H.; Nonaka, H.; Sumiyoshi, A.; Taki, Y. Prevention of cancer recurrence in tumor margins by stopping microcirculation in the tumor and tumor-host interface Cancer Sci. 2014, 105, 1196-1204 10.1111/cas.12477
-
(2014)
Cancer Sci.
, vol.105
, pp. 1196-1204
-
-
Hori, K.1
Akita, H.2
Nonaka, H.3
Sumiyoshi, A.4
Taki, Y.5
-
173
-
-
84949089411
-
Combretastatin A4 phosphate treatment induces vasculogenic mimicry formation of W256 breast carcinoma tumor in vitro and in vivo
-
Yao, N.; Ren, K.; Jiang, C.; Gao, M.; Huang, D.; Lu, X.; Lou, B.; Peng, F.; Yang, A.; Wang, X.; Ni, Y.; Zhang, J. Combretastatin A4 phosphate treatment induces vasculogenic mimicry formation of W256 breast carcinoma tumor in vitro and in vivo Tumor Biol. 2015, 36, 8499-8510 10.1007/s13277-015-3508-x
-
(2015)
Tumor Biol.
, vol.36
, pp. 8499-8510
-
-
Yao, N.1
Ren, K.2
Jiang, C.3
Gao, M.4
Huang, D.5
Lu, X.6
Lou, B.7
Peng, F.8
Yang, A.9
Wang, X.10
Ni, Y.11
Zhang, J.12
-
174
-
-
14844325322
-
Tumour parameters affected by combretastatin A-4 phosphate therapy in a human colorectal xenograft model in nude mice
-
El-Emir, E.; Boxer, G. M.; Petrie, I. A.; Boden, R. W.; Dearling, J. L. J.; Begent, R. H. J.; Pedley, R. B. Tumour parameters affected by combretastatin A-4 phosphate therapy in a human colorectal xenograft model in nude mice Eur. J. Cancer 2005, 41, 799-806 10.1016/j.ejca.2005.01.001
-
(2005)
Eur. J. Cancer
, vol.41
, pp. 799-806
-
-
El-Emir, E.1
Boxer, G.M.2
Petrie, I.A.3
Boden, R.W.4
Dearling, J.L.J.5
Begent, R.H.J.6
Pedley, R.B.7
-
175
-
-
33845914327
-
Anti-vascular agent Combretastatin A-4-P modulates hypoxia inducible factor-1 and gene expression
-
Dachs, G. U.; Steele, A. J.; Coralli, C.; Kanthou, C.; Brooks, A. C.; Gunningham, S. P.; Currie, M. J.; Watson, A. I.; Robinson, B. A.; Tozer, G. M. Anti-vascular agent Combretastatin A-4-P modulates hypoxia inducible factor-1 and gene expression BMC Cancer 2006, 6, 280 10.1186/1471-2407-6-280
-
(2006)
BMC Cancer
, vol.6
, pp. 280
-
-
Dachs, G.U.1
Steele, A.J.2
Coralli, C.3
Kanthou, C.4
Brooks, A.C.5
Gunningham, S.P.6
Currie, M.J.7
Watson, A.I.8
Robinson, B.A.9
Tozer, G.M.10
-
176
-
-
12944253116
-
Expression of VEGFR-2 and AC133 by circulating human CD34+ cells identifies a population of functional endothelial precursors
-
Peichev, M.; Naiyer, A. J.; Pereira, D.; Zhu, Z.; Lane, W. J.; Williams, M.; Oz, M. C.; Hicklin, D. J.; Witte, L.; Moore, M. A. S.; Rafii, S. Expression of VEGFR-2 and AC133 by circulating human CD34+ cells identifies a population of functional endothelial precursors Blood 2000, 95, 952-958
-
(2000)
Blood
, vol.95
, pp. 952-958
-
-
Peichev, M.1
Naiyer, A.J.2
Pereira, D.3
Zhu, Z.4
Lane, W.J.5
Williams, M.6
Oz, M.C.7
Hicklin, D.J.8
Witte, L.9
Moore, M.A.S.10
Rafii, S.11
-
177
-
-
34250719709
-
Bone marrow-derived endothelial progenitor cells are a major determinant of nascent tumor neovascularization
-
Nolan, D. J.; Ciarrocchi, A.; Mellick, A. S.; Jaggi, J. S.; Bambino, K.; Gupta, S.; Heikamp, E.; McDevitt, M. R.; Scheinberg, D. A.; Benezra, R.; Mittal, V. Bone marrow-derived endothelial progenitor cells are a major determinant of nascent tumor neovascularization Genes Dev. 2007, 21, 1546-1558 10.1101/gad.436307
-
(2007)
Genes Dev.
, vol.21
, pp. 1546-1558
-
-
Nolan, D.J.1
Ciarrocchi, A.2
Mellick, A.S.3
Jaggi, J.S.4
Bambino, K.5
Gupta, S.6
Heikamp, E.7
McDevitt, M.R.8
Scheinberg, D.A.9
Benezra, R.10
Mittal, V.11
-
178
-
-
4043184065
-
Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1
-
Ceradini, D. J.; Kulkarni, A. R.; Callaghan, M. J.; Tepper, O. M.; Bastidas, N.; Kleinman, M. E.; Capla, J. M.; Galiano, R. D.; Levine, J. P.; Gurtner, G. C. Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1 Nat. Med. 2004, 10, 858-864 10.1038/nm1075
-
(2004)
Nat. Med.
, vol.10
, pp. 858-864
-
-
Ceradini, D.J.1
Kulkarni, A.R.2
Callaghan, M.J.3
Tepper, O.M.4
Bastidas, N.5
Kleinman, M.E.6
Capla, J.M.7
Galiano, R.D.8
Levine, J.P.9
Gurtner, G.C.10
-
179
-
-
84898959067
-
Role of endothelial progenitor cells in cancer progression
-
Moschetta, M.; Mishima, Y.; Sahin, I.; Manier, S.; Glavey, S.; Vacca, A.; Roccaro, A. M.; Ghobrial, I. M. Role of endothelial progenitor cells in cancer progression Biochim. Biophys. Acta, Rev. Cancer 2014, 1846, 26-39 10.1016/j.bbcan.2014.03.005
-
(2014)
Biochim. Biophys. Acta, Rev. Cancer
, vol.1846
, pp. 26-39
-
-
Moschetta, M.1
Mishima, Y.2
Sahin, I.3
Manier, S.4
Glavey, S.5
Vacca, A.6
Roccaro, A.M.7
Ghobrial, I.M.8
-
180
-
-
70350220627
-
Contribution of granulocyte colony-stimulating factor to the acute mobilization of endothelial precursor cells by vascular disrupting agents
-
Shaked, Y.; Tang, T.; Woloszynek, J.; Daenen, L. G.; Man, S.; Xu, P.; Cai, S. R.; Arbeit, J. M.; Voest, E. E.; Chaplin, D. J.; Smythe, J.; Harris, A.; Nathan, P.; Judson, I.; Rustin, G.; Bertolini, F.; Link, D. C.; Kerbel, R. S. Contribution of granulocyte colony-stimulating factor to the acute mobilization of endothelial precursor cells by vascular disrupting agents Cancer Res. 2009, 69, 7524-7528 10.1158/0008-5472.CAN-09-0381
-
(2009)
Cancer Res.
, vol.69
, pp. 7524-7528
-
-
Shaked, Y.1
Tang, T.2
Woloszynek, J.3
Daenen, L.G.4
Man, S.5
Xu, P.6
Cai, S.R.7
Arbeit, J.M.8
Voest, E.E.9
Chaplin, D.J.10
Smythe, J.11
Harris, A.12
Nathan, P.13
Judson, I.14
Rustin, G.15
Bertolini, F.16
Link, D.C.17
Kerbel, R.S.18
-
181
-
-
33749005405
-
Therapy-induced acute recruitment of circulating endothelial progenitor cells to tumors
-
Shaked, Y.; Ciarrocchi, A.; Franco, M.; Lee, C. R.; Man, S.; Cheung, A. M.; Hicklin, D. J.; Chaplin, D.; Foster, F. S.; Benezra, R.; Kerbel, R. S. Therapy-induced acute recruitment of circulating endothelial progenitor cells to tumors Science 2006, 313, 1785-1787 10.1126/science.1127592
-
(2006)
Science
, vol.313
, pp. 1785-1787
-
-
Shaked, Y.1
Ciarrocchi, A.2
Franco, M.3
Lee, C.R.4
Man, S.5
Cheung, A.M.6
Hicklin, D.J.7
Chaplin, D.8
Foster, F.S.9
Benezra, R.10
Kerbel, R.S.11
-
182
-
-
34548798765
-
Tie2-expressing monocytes and tumor angiogenesis: Regulation by hypoxia and angiopoietin-2
-
Lewis, C. E.; De Palma, M.; Naldini, L. Tie2-expressing monocytes and tumor angiogenesis: Regulation by hypoxia and angiopoietin-2 Cancer Res. 2007, 67, 8429-8432 10.1158/0008-5472.CAN-07-1684
-
(2007)
Cancer Res.
, vol.67
, pp. 8429-8432
-
-
Lewis, C.E.1
De Palma, M.2
Naldini, L.3
-
183
-
-
79955517032
-
TIE2-expressing macrophages limit the therapeutic efficacy of the vascular-disrupting agent combretastatin A4 phosphate in mice
-
Welford, A. F.; Biziato, D.; Coffelt, S. B.; Nucera, S.; Fisher, M.; Pucci, F.; Di Serio, C.; Naldini, L.; De Palma, M.; Tozer, G. M.; Lewis, C. E. TIE2-expressing macrophages limit the therapeutic efficacy of the vascular-disrupting agent combretastatin A4 phosphate in mice J. Clin. Invest. 2011, 121, 1969-1973 10.1172/JCI44562
-
(2011)
J. Clin. Invest.
, vol.121
, pp. 1969-1973
-
-
Welford, A.F.1
Biziato, D.2
Coffelt, S.B.3
Nucera, S.4
Fisher, M.5
Pucci, F.6
Di Serio, C.7
Naldini, L.8
De Palma, M.9
Tozer, G.M.10
Lewis, C.E.11
-
184
-
-
0033817283
-
Determinants of anti-vascular action by combretastatin A-4 phosphate: Role of nitric oxide
-
Parkins, C. S.; Holder, A. L.; Hill, S. A.; Chaplin, D. J.; Tozer, G. M. Determinants of anti-vascular action by combretastatin A-4 phosphate: Role of nitric oxide Br. J. Cancer 2000, 83, 811-816 10.1054/bjoc.2000.1361
-
(2000)
Br. J. Cancer
, vol.83
, pp. 811-816
-
-
Parkins, C.S.1
Holder, A.L.2
Hill, S.A.3
Chaplin, D.J.4
Tozer, G.M.5
-
185
-
-
84907856513
-
A combretastatin-mediated decrease in neutrophil concentration in peripheral blood and the impact on the anti-tumor activity of this drug in two different murine tumor models
-
Bohn, A. B.; Wittenborn, T.; Brems-Eskildsen, A. S.; Laurberg, T.; Bertelsen, L. B.; Nielsen, T.; Stødkilde-Jørgensen, H.; Møller, B. K.; Horsman, M. R. A combretastatin-mediated decrease in neutrophil concentration in peripheral blood and the impact on the anti-tumor activity of this drug in two different murine tumor models PLoS One 2014, 9, e110091 10.1371/journal.pone.0110091
-
(2014)
PLoS One
, vol.9
, pp. e110091
-
-
Bohn, A.B.1
Wittenborn, T.2
Brems-Eskildsen, A.S.3
Laurberg, T.4
Bertelsen, L.B.5
Nielsen, T.6
Stødkilde-Jørgensen, H.7
Møller, B.K.8
Horsman, M.R.9
-
186
-
-
84864408336
-
The vascular targeting agent Combretastatin-A4 directly induces autophagy in adenocarcinoma-derived colon cancer cells
-
Greene, L. M.; O'Boyle, N. M.; Nolan, D. P.; Meegan, M. J.; Zisterer, D. M. The vascular targeting agent Combretastatin-A4 directly induces autophagy in adenocarcinoma-derived colon cancer cells Biochem. Pharmacol. 2012, 84, 612-624 10.1016/j.bcp.2012.06.005
-
(2012)
Biochem. Pharmacol.
, vol.84
, pp. 612-624
-
-
Greene, L.M.1
O'Boyle, N.M.2
Nolan, D.P.3
Meegan, M.J.4
Zisterer, D.M.5
-
187
-
-
84891047905
-
Autophagy blockade sensitizes the anticancer activity of CA-4 via JNK-Bcl-2 pathway
-
Li, Y.; Luo, P.; Wang, J.; Dai, J.; Yang, X.; Wu, H.; Yang, B.; He, Q. Autophagy blockade sensitizes the anticancer activity of CA-4 via JNK-Bcl-2 pathway Toxicol. Appl. Pharmacol. 2014, 274, 319-327 10.1016/j.taap.2013.11.018
-
(2014)
Toxicol. Appl. Pharmacol.
, vol.274
, pp. 319-327
-
-
Li, Y.1
Luo, P.2
Wang, J.3
Dai, J.4
Yang, X.5
Wu, H.6
Yang, B.7
He, Q.8
-
188
-
-
84879554909
-
The vascular disrupting agent ombrabulin (AVE8062) enhances the efficacy of standard therapies in head and neck squamous cell carcinoma xenograft models
-
Clémenson, C.; Jouannot, E.; Merino-Trigo, A.; Rubin-Carrez, C.; Deutsch, E. The vascular disrupting agent ombrabulin (AVE8062) enhances the efficacy of standard therapies in head and neck squamous cell carcinoma xenograft models Invest. New Drugs 2013, 31, 273-284 10.1007/s10637-012-9852-4
-
(2013)
Invest. New Drugs
, vol.31
, pp. 273-284
-
-
Clémenson, C.1
Jouannot, E.2
Merino-Trigo, A.3
Rubin-Carrez, C.4
Deutsch, E.5
-
189
-
-
34948862788
-
Sequence dependent antitumour efficacy of the vascular disrupting agent ZD6126 in combination with paclitaxel
-
Martinelli, M.; Bonezzi, K.; Riccardi, E.; Kuhn, E.; Frapolli, R.; Zucchetti, M.; Ryan, A. J.; Taraboletti, G.; Giavazzi, R. Sequence dependent antitumour efficacy of the vascular disrupting agent ZD6126 in combination with paclitaxel Br. J. Cancer 2007, 97, 888-894 10.1038/sj.bjc.6603969
-
(2007)
Br. J. Cancer
, vol.97
, pp. 888-894
-
-
Martinelli, M.1
Bonezzi, K.2
Riccardi, E.3
Kuhn, E.4
Frapolli, R.5
Zucchetti, M.6
Ryan, A.J.7
Taraboletti, G.8
Giavazzi, R.9
-
190
-
-
84875399800
-
Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
-
Wu, X. Y.; Ma, W.; Gurung, K.; Guo, C. H. Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy J. Formosan Med. Assoc. 2013, 112, 115-124 10.1016/j.jfma.2012.09.017
-
(2013)
J. Formosan Med. Assoc.
, vol.112
, pp. 115-124
-
-
Wu, X.Y.1
Ma, W.2
Gurung, K.3
Guo, C.H.4
-
191
-
-
84862532904
-
Phase i trial of combretastatin A4 phosphate (CA4P) in combination with bevacizumab in patients with advanced cancer
-
Nathan, P.; Zweifel, M.; Padhani, A. R.; Koh, D. M.; Ng, M.; Collins, D. J.; Harris, A.; Carden, C.; Smythe, J.; Fisher, N.; Taylor, N. J.; Stirling, J. J.; Lu, S. P.; Leach, M. O.; Rustin, G. J. S.; Judson, I. Phase I trial of combretastatin A4 phosphate (CA4P) in combination with bevacizumab in patients with advanced cancer Clin. Cancer Res. 2012, 18, 3428-3439 10.1158/1078-0432.CCR-11-3376
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 3428-3439
-
-
Nathan, P.1
Zweifel, M.2
Padhani, A.R.3
Koh, D.M.4
Ng, M.5
Collins, D.J.6
Harris, A.7
Carden, C.8
Smythe, J.9
Fisher, N.10
Taylor, N.J.11
Stirling, J.J.12
Lu, S.P.13
Leach, M.O.14
Rustin, G.J.S.15
Judson, I.16
-
192
-
-
84907969444
-
The multifaceted activity of VEGF in angiogenesis - Implications for therapy responses
-
Moens, S.; Goveia, J.; Stapor, P. C.; Cantelmo, A. R.; Carmeliet, P. The multifaceted activity of VEGF in angiogenesis-Implications for therapy responses Cytokine Growth Factor Rev. 2014, 25, 473-482 10.1016/j.cytogfr.2014.07.009
-
(2014)
Cytokine Growth Factor Rev.
, vol.25
, pp. 473-482
-
-
Moens, S.1
Goveia, J.2
Stapor, P.C.3
Cantelmo, A.R.4
Carmeliet, P.5
-
193
-
-
84875998274
-
Markers of response for the antiangiogenic agent bevacizumab
-
Lambrechts, D.; Lenz, H. J.; De Haas, S.; Carmeliet, P.; Scherer, S. J. Markers of response for the antiangiogenic agent bevacizumab J. Clin. Oncol. 2013, 31, 1219-1230 10.1200/JCO.2012.46.2762
-
(2013)
J. Clin. Oncol.
, vol.31
, pp. 1219-1230
-
-
Lambrechts, D.1
Lenz, H.J.2
De Haas, S.3
Carmeliet, P.4
Scherer, S.J.5
-
194
-
-
79953648492
-
Phase II trial of combretastatin A4 phosphate, carboplatin, and paclitaxel in patients with platinum-resistant ovarian cancer
-
Zweifel, M.; Jayson, G. C.; Reed, N. S.; Osborne, R.; Hassan, B.; Ledermann, J.; Shreeves, G.; Poupard, L.; Lu, S. P.; Balkissoon, J.; Chaplin, D. J.; Rustin, G. J. S. Phase II trial of combretastatin A4 phosphate, carboplatin, and paclitaxel in patients with platinum-resistant ovarian cancer Ann. Oncol. 2011, 22, 2036-2041 10.1093/annonc/mdq708
-
(2011)
Ann. Oncol.
, vol.22
, pp. 2036-2041
-
-
Zweifel, M.1
Jayson, G.C.2
Reed, N.S.3
Osborne, R.4
Hassan, B.5
Ledermann, J.6
Shreeves, G.7
Poupard, L.8
Lu, S.P.9
Balkissoon, J.10
Chaplin, D.J.11
Rustin, G.J.S.12
-
195
-
-
84869399605
-
Thyroidectomy followed by fosbretabulin (CA4P) combination regimen appears to suggest improvement in patient survival in anaplastic thyroid cancer
-
Sosa, J. A.; Balkissoon, J.; Lu, S. P.; Langecker, P.; Elisei, R.; Jarzab, B.; Bal, C. S.; Marur, S.; Gramza, A.; Ondrey, F. Thyroidectomy followed by fosbretabulin (CA4P) combination regimen appears to suggest improvement in patient survival in anaplastic thyroid cancer Surgery 2012, 152, 1078-1087 10.1016/j.surg.2012.08.036
-
(2012)
Surgery
, vol.152
, pp. 1078-1087
-
-
Sosa, J.A.1
Balkissoon, J.2
Lu, S.P.3
Langecker, P.4
Elisei, R.5
Jarzab, B.6
Bal, C.S.7
Marur, S.8
Gramza, A.9
Ondrey, F.10
-
196
-
-
84904102075
-
DISRUPT: A randomised phase 2 trial of ombrabulin (AVE8062) plus a taxane-platinum regimen as first-line therapy for metastatic non-small cell lung cancer
-
von Pawel, J.; Gorbounova, V.; Reck, M.; Kowalski, D. M.; Allard, A.; Chadjaa, M.; Rey, A.; Bennouna, J.; Grossi, F. DISRUPT: A randomised phase 2 trial of ombrabulin (AVE8062) plus a taxane-platinum regimen as first-line therapy for metastatic non-small cell lung cancer Lung Cancer 2014, 85, 224-229 10.1016/j.lungcan.2014.05.013
-
(2014)
Lung Cancer
, vol.85
, pp. 224-229
-
-
Von Pawel, J.1
Gorbounova, V.2
Reck, M.3
Kowalski, D.M.4
Allard, A.5
Chadjaa, M.6
Rey, A.7
Bennouna, J.8
Grossi, F.9
-
197
-
-
0036568457
-
Vascular targeting agents enhance chemotherapeutic agent activities in solid tumor therapy
-
Siemann, D. W.; Mercer, E.; Lepler, S.; Rojiani, A. M. Vascular targeting agents enhance chemotherapeutic agent activities in solid tumor therapy Int. J. Cancer 2002, 99, 1-6 10.1002/ijc.10316
-
(2002)
Int. J. Cancer
, vol.99
, pp. 1-6
-
-
Siemann, D.W.1
Mercer, E.2
Lepler, S.3
Rojiani, A.M.4
-
198
-
-
20044395276
-
Phase i trial of combretastatin A-4 phosphate with carboplatin
-
Bilenker, J. H.; Flaherty, K. T.; Rosen, M.; Davis, L.; Gallagher, M.; Stevenson, J. P.; Sun, W.; Vaughn, D.; Giantonio, B.; Zimmer, R.; Schnall, M.; O'Dwyer, P. J. Phase I trial of combretastatin A-4 phosphate with carboplatin Clin. Cancer Res. 2005, 11, 1527-1533 10.1158/1078-0432.CCR-04-1434
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 1527-1533
-
-
Bilenker, J.H.1
Flaherty, K.T.2
Rosen, M.3
Davis, L.4
Gallagher, M.5
Stevenson, J.P.6
Sun, W.7
Vaughn, D.8
Giantonio, B.9
Zimmer, R.10
Schnall, M.11
O'Dwyer, P.J.12
-
199
-
-
84918514058
-
The contribution of αβ-tubulin curvature to microtubule dynamics
-
Brouhard, G. J.; Rice, L. M. The contribution of αβ-tubulin curvature to microtubule dynamics J. Cell Biol. 2014, 207, 323-334 10.1083/jcb.201407095
-
(2014)
J. Cell Biol.
, vol.207
, pp. 323-334
-
-
Brouhard, G.J.1
Rice, L.M.2
-
200
-
-
0033119771
-
Combretastatin A-4 phosphate as a tumor vascular-targeting agent: Early effects in tumors and normal tissues
-
Tozer, G. M.; Prise, V. E.; Wilson, J.; Locke, R. J.; Vojnovic, B.; Stratford, M. R. L.; Dennis, M. F.; Chaplin, D. J. Combretastatin A-4 phosphate as a tumor vascular-targeting agent: Early effects in tumors and normal tissues Cancer Res. 1999, 59, 1626-1634
-
(1999)
Cancer Res.
, vol.59
, pp. 1626-1634
-
-
Tozer, G.M.1
Prise, V.E.2
Wilson, J.3
Locke, R.J.4
Vojnovic, B.5
Stratford, M.R.L.6
Dennis, M.F.7
Chaplin, D.J.8
-
201
-
-
84892414410
-
Vascular RhoJ is an effective and selective target for tumor angiogenesis and vascular disruption
-
Kim, C.; Yang, H.; Fukushima, Y.; Saw, P.; Lee, J.; Park, J. S.; Park, I.; Jung, J.; Kataoka, H.; Lee, D.; DoHeo, W.; Kim, I.; Jon, S.; Adams, R. H.; Nishikawa, S. I.; Uemura, A.; Koh, G. Vascular RhoJ is an effective and selective target for tumor angiogenesis and vascular disruption Cancer Cell 2014, 25, 102-117 10.1016/j.ccr.2013.12.010
-
(2014)
Cancer Cell
, vol.25
, pp. 102-117
-
-
Kim, C.1
Yang, H.2
Fukushima, Y.3
Saw, P.4
Lee, J.5
Park, J.S.6
Park, I.7
Jung, J.8
Kataoka, H.9
Lee, D.10
DoHeo, W.11
Kim, I.12
Jon, S.13
Adams, R.H.14
Nishikawa, S.I.15
Uemura, A.16
Koh, G.17
-
202
-
-
40349091426
-
P38 MAPK, but not ERK1/2, is critically involved in the cytotoxicity of the novel vascular disrupting agent combretastatin A4
-
Quan, H.; Xu, Y.; Lou, L. p38 MAPK, but not ERK1/2, is critically involved in the cytotoxicity of the novel vascular disrupting agent combretastatin A4 Int. J. Cancer 2008, 122, 1730-1737 10.1002/ijc.23262
-
(2008)
Int. J. Cancer
, vol.122
, pp. 1730-1737
-
-
Quan, H.1
Xu, Y.2
Lou, L.3
-
203
-
-
84948411384
-
Smart nanosystems: Bio-inspired technologies that interact with the host environment
-
Kwon, E. J.; Lo, J. H.; Bhatia, S. N. Smart nanosystems: Bio-inspired technologies that interact with the host environment Proc. Natl. Acad. Sci. U. S. A. 2015, 112, 14460-14466 10.1073/pnas.1508522112
-
(2015)
Proc. Natl. Acad. Sci. U. S. A.
, vol.112
, pp. 14460-14466
-
-
Kwon, E.J.1
Lo, J.H.2
Bhatia, S.N.3
-
204
-
-
84915809304
-
Drug-induced amplification of nanoparticle targeting to tumors
-
Lin, K. Y.; Kwon, E. J.; Lo, J. H.; Bhatia, S. N. Drug-induced amplification of nanoparticle targeting to tumors Nano Today 2014, 9, 550-559 10.1016/j.nantod.2014.09.001
-
(2014)
Nano Today
, vol.9
, pp. 550-559
-
-
Lin, K.Y.1
Kwon, E.J.2
Lo, J.H.3
Bhatia, S.N.4
|