-
1
-
-
84920703518
-
Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013
-
GBD 2013 Mortality and Causes of Death Collaborators. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2015; 385:117-171.
-
(2015)
Lancet
, vol.385
, pp. 117-171
-
-
-
2
-
-
84918815964
-
Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012
-
Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D, Bray F. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015; 136:E359-E386.
-
(2015)
Int J Cancer
, vol.136
, pp. E359-E386
-
-
Ferlay, J.1
Soerjomataram, I.2
Dikshit, R.3
Eser, S.4
Mathers, C.5
Rebelo, M.6
Parkin, D.M.7
Forman, D.8
Bray, F.9
-
3
-
-
84899484919
-
Annual Report to the Nation on the status of cancer, 1975-2010, featuring prevalence of comorbidity and impact on survival among persons with lung, colorectal, breast, or prostate cancer
-
Edwards BK, Noone AM, Mariotto AB, Simard EP, Boscoe FP, Henley SJ, Jemal A, Cho H, Anderson RN, Kohler BA, Eheman CR, Ward EM. Annual Report to the Nation on the status of cancer, 1975-2010, featuring prevalence of comorbidity and impact on survival among persons with lung, colorectal, breast, or prostate cancer. Cancer. 2014; 120:1290-1314.
-
(2014)
Cancer
, vol.120
, pp. 1290-1314
-
-
Edwards, B.K.1
Noone, A.M.2
Mariotto, A.B.3
Simard, E.P.4
Boscoe, F.P.5
Henley, S.J.6
Jemal, A.7
Cho, H.8
Anderson, R.N.9
Kohler, B.A.10
Eheman, C.R.11
Ward, E.M.12
-
4
-
-
84875404870
-
How can attrition rates be reduced in cancer drug discovery?
-
Moreno L, Pearson AD. How can attrition rates be reduced in cancer drug discovery? Expert Opin Drug Discov. 2013; 8:363-368.
-
(2013)
Expert Opin Drug Discov
, vol.8
, pp. 363-368
-
-
Moreno, L.1
Pearson, A.D.2
-
5
-
-
84877579534
-
Drug attrition during pre-clinical and clinical development: understanding and managing drug-induced cardiotoxicity
-
Ferri N, Siegl P, Corsini A, Herrmann J, Lerman A, Benghozi R. Drug attrition during pre-clinical and clinical development: understanding and managing drug-induced cardiotoxicity. Pharmacol Ther. 2013; 138:470-484.
-
(2013)
Pharmacol Ther
, vol.138
, pp. 470-484
-
-
Ferri, N.1
Siegl, P.2
Corsini, A.3
Herrmann, J.4
Lerman, A.5
Benghozi, R.6
-
6
-
-
73449101512
-
Lessons from 60 years of pharmaceutical innovation
-
Munos B. Lessons from 60 years of pharmaceutical innovation. Nat Rev Drug Discov. 2009; 8:959-968.
-
(2009)
Nat Rev Drug Discov
, vol.8
, pp. 959-968
-
-
Munos, B.1
-
7
-
-
0032748385
-
Antitumor activity of thalidomide in refractory multiple myeloma.[Erratum appears in N Engl J Med 2000 Feb 3;342:364]
-
Singhal S, Mehta J, Desikan R, Ayers D, Roberson P, Eddlemon P, Munshi N, Anaissie E, Wilson C, Dhodapkar M, Zeddis J, Barlogie B. Antitumor activity of thalidomide in refractory multiple myeloma.[Erratum appears in N Engl J Med 2000 Feb 3;342:364]. N Engl J Med. 1999; 341:1565-1571.
-
(1999)
N Engl J Med
, vol.341
, pp. 1565-1571
-
-
Singhal, S.1
Mehta, J.2
Desikan, R.3
Ayers, D.4
Roberson, P.5
Eddlemon, P.6
Munshi, N.7
Anaissie, E.8
Wilson, C.9
Dhodapkar, M.10
Zeddis, J.11
Barlogie, B.12
-
8
-
-
84919363339
-
Repurposing of bisphosphonates for the prevention and therapy of nonsmall cell lung and breast cancer
-
Stachnik A, Yuen T, Iqbal J, Sgobba M, Gupta Y, Lu P, Colaianni G, Ji Y, Zhu LL, Kim SM, Li J, Liu P, Izadmehr S, et al. Repurposing of bisphosphonates for the prevention and therapy of nonsmall cell lung and breast cancer. Proc Natl Acad Sci USA. 2014; 111:17995-18000.
-
(2014)
Proc Natl Acad Sci USA
, vol.111
, pp. 17995-18000
-
-
Stachnik, A.1
Yuen, T.2
Iqbal, J.3
Sgobba, M.4
Gupta, Y.5
Lu, P.6
Colaianni, G.7
Ji, Y.8
Zhu, L.L.9
Kim, S.M.10
Li, J.11
Liu, P.12
Izadmehr, S.13
-
9
-
-
84929465568
-
Selective antitumor activity of ibrutinib in EGFR-mutant non-small cell lung cancer cells
-
Gao W, Wang M, Wang L, Lu H, Wu S, Dai B, Ou Z, Zhang L, Heymach JV, Gold KA, Minna J, Roth JA, Hofstetter WL, et al. Selective antitumor activity of ibrutinib in EGFR-mutant non-small cell lung cancer cells. J Natl Cancer Inst. 2014; 106:dju204-.
-
(2014)
J Natl Cancer Inst
, vol.106
-
-
Gao, W.1
Wang, M.2
Wang, L.3
Lu, H.4
Wu, S.5
Dai, B.6
Ou, Z.7
Zhang, L.8
Heymach, J.V.9
Gold, K.A.10
Minna, J.11
Roth, J.A.12
Hofstetter, W.L.13
-
10
-
-
84890027846
-
A drug repositioning approach identifies tricyclic antidepressants as inhibitors of small cell lung cancer and other neuroendocrine tumors
-
Jahchan NS, Dudley JT, Mazur PK, Flores N, Yang D, Palmerton A, Zmoos AF, Vaka D, Tran KQ, Zhou M, Krasinska K, Riess JW, Neal JW, et al. A drug repositioning approach identifies tricyclic antidepressants as inhibitors of small cell lung cancer and other neuroendocrine tumors. Cancer Discov. 2013; 3:1364-1377.
-
(2013)
Cancer Discov
, vol.3
, pp. 1364-1377
-
-
Jahchan, N.S.1
Dudley, J.T.2
Mazur, P.K.3
Flores, N.4
Yang, D.5
Palmerton, A.6
Zmoos, A.F.7
Vaka, D.8
Tran, K.Q.9
Zhou, M.10
Krasinska, K.11
Riess, J.W.12
Neal, J.W.13
-
11
-
-
84883471209
-
KEAP1-dependent synthetic lethality induced by AKT and TXNRD1 inhibitors in lung cancer
-
Dai B, Yoo SY, Bartholomeusz G, Graham RA, Majidi M, Yan S, Meng J, Ji L, Coombes K, Minna JD, Fang B, Roth JA. KEAP1-dependent synthetic lethality induced by AKT and TXNRD1 inhibitors in lung cancer. Cancer Res. 2013; 73:5532-5543.
-
(2013)
Cancer Res
, vol.73
, pp. 5532-5543
-
-
Dai, B.1
Yoo, S.Y.2
Bartholomeusz, G.3
Graham, R.A.4
Majidi, M.5
Yan, S.6
Meng, J.7
Ji, L.8
Coombes, K.9
Minna, J.D.10
Fang, B.11
Roth, J.A.12
-
12
-
-
0021257099
-
Auranofin. A preliminary review of its pharmacological properties and therapeutic use in rheumatoid arthritis
-
Chaffman M, Brogden RN, Heel RC, Speight TM, Avery GS. Auranofin. A preliminary review of its pharmacological properties and therapeutic use in rheumatoid arthritis. Drugs. 1984; 27:378-424.
-
(1984)
Drugs
, vol.27
, pp. 378-424
-
-
Chaffman, M.1
Brogden, R.N.2
Heel, R.C.3
Speight, T.M.4
Avery, G.S.5
-
13
-
-
0023695479
-
The efficacy and safety of auranofin in the treatment of juvenile rheumatoid arthritis. A long-term open study
-
Marcolongo R, Mathieu A, Pala R, Giordano N, Fioravanti A, Panzarasa R. The efficacy and safety of auranofin in the treatment of juvenile rheumatoid arthritis. A long-term open study. Arthritis Rheumatism. 1988; 31:979-983.
-
(1988)
Arthritis Rheumatism
, vol.31
, pp. 979-983
-
-
Marcolongo, R.1
Mathieu, A.2
Pala, R.3
Giordano, N.4
Fioravanti, A.5
Panzarasa, R.6
-
15
-
-
0030855880
-
Auranofin is safe and superior to placebo in elderly-onset rheumatoid arthritis
-
Glennas A, Kvien TK, Andrup O, Clarke-Jenssen O, Karstensen B, Brodin U. Auranofin is safe and superior to placebo in elderly-onset rheumatoid arthritis. Br J Rheumatol. 1997; 36:870-877.
-
(1997)
Br J Rheumatol
, vol.36
, pp. 870-877
-
-
Glennas, A.1
Kvien, T.K.2
Andrup, O.3
Clarke-Jenssen, O.4
Karstensen, B.5
Brodin, U.6
-
17
-
-
84862015314
-
A highthroughput drug screen for Entamoeba histolytica identifies a new lead and target
-
Debnath A, Parsonage D, Andrade RM, He C, Cobo ER, Hirata K, Chen S, Garcia-Rivera G, Orozco E, Martinez MB, Gunatilleke SS, Barrios AM, Arkin MR, et al. A highthroughput drug screen for Entamoeba histolytica identifies a new lead and target. Nat Med. 2012; 18:956-960.
-
(2012)
Nat Med
, vol.18
, pp. 956-960
-
-
Debnath, A.1
Parsonage, D.2
Andrade, R.M.3
He, C.4
Cobo, E.R.5
Hirata, K.6
Chen, S.7
Garcia-Rivera, G.8
Orozco, E.9
Martinez, M.B.10
Gunatilleke, S.S.11
Barrios, A.M.12
Arkin, M.R.13
-
18
-
-
71749083138
-
Cancer cell death induced by phosphine gold(I) compounds targeting thioredoxin reductase
-
Gandin V, Fernandes AP, Rigobello MP, Dani B, Sorrentino F, Tisato F, Bjornstedt M, Bindoli A, Sturaro A, Rella R, Marzano C. Cancer cell death induced by phosphine gold(I) compounds targeting thioredoxin reductase. Biochem Pharmacol. 2010; 79:90-101.
-
(2010)
Biochem Pharmacol
, vol.79
, pp. 90-101
-
-
Gandin, V.1
Fernandes, A.P.2
Rigobello, M.P.3
Dani, B.4
Sorrentino, F.5
Tisato, F.6
Bjornstedt, M.7
Bindoli, A.8
Sturaro, A.9
Rella, R.10
Marzano, C.11
-
19
-
-
84862282802
-
Gold(I) carbene complexes causing thioredoxin 1 and thioredoxin 2 oxidation as potential anticancer agents
-
Schuh E, Pfluger C, Citta A, Folda A, Rigobello MP, Bindoli A, Casini A, Mohr F. Gold(I) carbene complexes causing thioredoxin 1 and thioredoxin 2 oxidation as potential anticancer agents. J Med Chem. 2012; 55:5518-5528.
-
(2012)
J Med Chem
, vol.55
, pp. 5518-5528
-
-
Schuh, E.1
Pfluger, C.2
Citta, A.3
Folda, A.4
Rigobello, M.P.5
Bindoli, A.6
Casini, A.7
Mohr, F.8
-
20
-
-
84880073554
-
Drug repurposing for gastrointestinal stromal tumor
-
Pessetto ZY, Weir SJ, Sethi G, Broward MA, Godwin AK. Drug repurposing for gastrointestinal stromal tumor. Mol Cancer Ther. 2013; 12:1299-1309.
-
(2013)
Mol Cancer Ther
, vol.12
, pp. 1299-1309
-
-
Pessetto, Z.Y.1
Weir, S.J.2
Sethi, G.3
Broward, M.A.4
Godwin, A.K.5
-
21
-
-
84857720818
-
Repurposing approved and abandoned drugs for the treatment and prevention of cancer through public-private partnership
-
Weir SJ, DeGennaro LJ, Austin CP. Repurposing approved and abandoned drugs for the treatment and prevention of cancer through public-private partnership. Cancer Res. 2012; 72:1055-1058.
-
(2012)
Cancer Res
, vol.72
, pp. 1055-1058
-
-
Weir, S.J.1
DeGennaro, L.J.2
Austin, C.P.3
-
22
-
-
84900019686
-
Auranofin induces lethal oxidative and endoplasmic reticulum stress and exerts potent preclinical activity against chronic lymphocytic leukemia
-
Fiskus W, Saba N, Shen M, Ghias M, Liu J, Gupta SD, Chauhan L, Rao R, Gunewardena S, Schorno K, Austin CP, Maddocks K, Byrd J, et al. Auranofin induces lethal oxidative and endoplasmic reticulum stress and exerts potent preclinical activity against chronic lymphocytic leukemia. Cancer Res. 2014; 74:2520-2532.
-
(2014)
Cancer Res
, vol.74
, pp. 2520-2532
-
-
Fiskus, W.1
Saba, N.2
Shen, M.3
Ghias, M.4
Liu, J.5
Gupta, S.D.6
Chauhan, L.7
Rao, R.8
Gunewardena, S.9
Schorno, K.10
Austin, C.P.11
Maddocks, K.12
Byrd, J.13
-
23
-
-
0021927358
-
Cancer in rheumatoid arthritis: a prospective long-term study of mortality
-
Fries JF, Bloch D, Spitz P, Mitchell DM. Cancer in rheumatoid arthritis: a prospective long-term study of mortality. Am J Med. 1985; 78:56-59.
-
(1985)
Am J Med
, vol.78
, pp. 56-59
-
-
Fries, J.F.1
Bloch, D.2
Spitz, P.3
Mitchell, D.M.4
-
24
-
-
84890541429
-
IGFBP2/FAK pathway is causally associated with dasatinib resistance in non-small cell lung cancer cells
-
Lu H, Wang L, Gao W, Meng J, Dai B, Wu S, Minna J, Roth JA, Hofstetter WL, Swisher SG, Fang B. IGFBP2/FAK pathway is causally associated with dasatinib resistance in non-small cell lung cancer cells. Mol Cancer Ther. 2013; 12:2864-2873.
-
(2013)
Mol Cancer Ther
, vol.12
, pp. 2864-2873
-
-
Lu, H.1
Wang, L.2
Gao, W.3
Meng, J.4
Dai, B.5
Wu, S.6
Minna, J.7
Roth, J.A.8
Hofstetter, W.L.9
Swisher, S.G.10
Fang, B.11
-
26
-
-
84898027331
-
Mixed lineage kinase domain-like protein MLKL causes necrotic membrane disruption upon phosphorylation by RIP3
-
Wang H, Sun L, Su L, Rizo J, Liu L, Wang LF, Wang FS, Wang X. Mixed lineage kinase domain-like protein MLKL causes necrotic membrane disruption upon phosphorylation by RIP3. Mol Cell. 2014; 54:133-146.
-
(2014)
Mol Cell
, vol.54
, pp. 133-146
-
-
Wang, H.1
Sun, L.2
Su, L.3
Rizo, J.4
Liu, L.5
Wang, L.F.6
Wang, F.S.7
Wang, X.8
-
27
-
-
33751178410
-
The thioredoxin system in cancer
-
Arner ES, Holmgren A. The thioredoxin system in cancer. Semin Cancer Biol. 2006; 16:420-426.
-
(2006)
Semin Cancer Biol
, vol.16
, pp. 420-426
-
-
Arner, E.S.1
Holmgren, A.2
-
28
-
-
67349120863
-
Focus on mammalian thioredoxin reductases-important selenoproteins with versatile functions
-
Arner ES. Focus on mammalian thioredoxin reductases-important selenoproteins with versatile functions. Biochim Biophys Acta. 2009; 1790:495-526.
-
(2009)
Biochim Biophys Acta
, vol.1790
, pp. 495-526
-
-
Arner, E.S.1
-
29
-
-
84872151251
-
The biological activity of auranofin: implications for novel treatment of diseases
-
Madeira JM, Gibson DL, Kean WF, Klegeris A. The biological activity of auranofin: implications for novel treatment of diseases. Inflammopharmacology. 2012; 20:297-306.
-
(2012)
Inflammopharmacology
, vol.20
, pp. 297-306
-
-
Madeira, J.M.1
Gibson, D.L.2
Kean, W.F.3
Klegeris, A.4
-
30
-
-
67650550815
-
Inhibiting JNK dephosphorylation and induction of apoptosis by novel anticancer agent NSC-741909 in cancer cells
-
Wei X, Guo W, Wu S, Wang L, Lu Y, Xu B, Liu J, Fang B. Inhibiting JNK dephosphorylation and induction of apoptosis by novel anticancer agent NSC-741909 in cancer cells. J Biol Chem. 2009; 284:16948-16955.
-
(2009)
J Biol Chem
, vol.284
, pp. 16948-16955
-
-
Wei, X.1
Guo, W.2
Wu, S.3
Wang, L.4
Lu, Y.5
Xu, B.6
Liu, J.7
Fang, B.8
-
31
-
-
84863076111
-
Aberrant expression of proteins involved in signal transduction and DNA repair pathways in lung cancer and their association with clinical parameters
-
He Y, Zhou Z, Hofstetter WL, Zhou Y, Hu W, Guo C, Wang L, Guo W, Pataer A, Correa AM, Lu Y, Wang J, Diao L, et al. Aberrant expression of proteins involved in signal transduction and DNA repair pathways in lung cancer and their association with clinical parameters. PLoS ONE. 2012; 7:e31087.
-
(2012)
PLoS ONE
, vol.7
-
-
He, Y.1
Zhou, Z.2
Hofstetter, W.L.3
Zhou, Y.4
Hu, W.5
Guo, C.6
Wang, L.7
Guo, W.8
Pataer, A.9
Correa, A.M.10
Lu, Y.11
Wang, J.12
Diao, L.13
-
32
-
-
78751705649
-
The gold compound auranofin induces apoptosis of human multiple myeloma cells through both down-regulation of STAT3 and inhibition of NF-kB activity
-
Nakaya A, Sagawa M, Muto A, Uchida H, Ikeda Y, Kizaki M. The gold compound auranofin induces apoptosis of human multiple myeloma cells through both down-regulation of STAT3 and inhibition of NF-kB activity. Leukemia Res. 2011; 35:243-249.
-
(2011)
Leukemia Res
, vol.35
, pp. 243-249
-
-
Nakaya, A.1
Sagawa, M.2
Muto, A.3
Uchida, H.4
Ikeda, Y.5
Kizaki, M.6
-
33
-
-
84907880426
-
Suppression of the pro-inflammatory NLRP3/interleukin-1beta pathway in macrophages by the thioredoxin reductase inhibitor auranofin
-
Isakov E, Weisman-Shomer P, Benhar M. Suppression of the pro-inflammatory NLRP3/interleukin-1beta pathway in macrophages by the thioredoxin reductase inhibitor auranofin. Biochim Biophys Acta. 2014; 1840: 3153-3161.
-
(2014)
Biochim Biophys Acta
, vol.1840
, pp. 3153-3161
-
-
Isakov, E.1
Weisman-Shomer, P.2
Benhar, M.3
-
34
-
-
84906249813
-
Clinically used antirheumatic agent auranofin is a proteasomal deubiquitinase inhibitor and inhibits tumor growth
-
Liu N, Li X, Huang H, Zhao C, Liao S, Yang C, Liu S, Song W, Lu X, Lan X, Chen X, Yi S, Xu L, et al. Clinically used antirheumatic agent auranofin is a proteasomal deubiquitinase inhibitor and inhibits tumor growth. Oncotarget. 2014; 5:5453-5471. doi: 10.18632/oncotarget.2113.
-
(2014)
Oncotarget
, vol.5
, pp. 5453-5471
-
-
Liu, N.1
Li, X.2
Huang, H.3
Zhao, C.4
Liao, S.5
Yang, C.6
Liu, S.7
Song, W.8
Lu, X.9
Lan, X.10
Chen, X.11
Yi, S.12
Xu, L.13
-
35
-
-
46249116457
-
Arsenic trioxide and auranofin inhibit selenoprotein synthesis: implications for chemotherapy for acute promyelocytic leukaemia
-
Talbot S, Nelson R, Self WT. Arsenic trioxide and auranofin inhibit selenoprotein synthesis: implications for chemotherapy for acute promyelocytic leukaemia. Br J Pharmacol. 2008; 154:940-948.
-
(2008)
Br J Pharmacol
, vol.154
, pp. 940-948
-
-
Talbot, S.1
Nelson, R.2
Self, W.T.3
-
36
-
-
84886787846
-
Systematic identification of molecular subtype-selective vulnerabilities in non-smallcell lung cancer
-
Kim HS, Mendiratta S, Kim J, Pecot CV, Larsen JE, Zubovych I, Seo BY, Kim J, Eskiocak B, Chung H, McMillan E, Wu S, De BJ, et al. Systematic identification of molecular subtype-selective vulnerabilities in non-smallcell lung cancer. Cell. 2013; 155:552-566.
-
(2013)
Cell
, vol.155
, pp. 552-566
-
-
Kim, H.S.1
Mendiratta, S.2
Kim, J.3
Pecot, C.V.4
Larsen, J.E.5
Zubovych, I.6
Seo, B.Y.7
Kim, J.8
Eskiocak, B.9
Chung, H.10
McMillan, E.11
Wu, S.12
De, B.J.13
-
37
-
-
84868628069
-
Mutations and deregulation of Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR cascades which alter therapy response
-
McCubrey JA, Steelman LS, Chappell WH, Abrams SL, Montalto G, Cervello M, Nicoletti F, Fagone P, Malaponte G, Mazzarino MC, Candido S, Libra M, Basecke J, et al. Mutations and deregulation of Ras/Raf/MEK/ERK and PI3K/PTEN/Akt/mTOR cascades which alter therapy response. Oncotarget. 2012; 3:954-987. doi: 10.18632/oncotarget.652.
-
(2012)
Oncotarget
, vol.3
, pp. 954-987
-
-
McCubrey, J.A.1
Steelman, L.S.2
Chappell, W.H.3
Abrams, S.L.4
Montalto, G.5
Cervello, M.6
Nicoletti, F.7
Fagone, P.8
Malaponte, G.9
Mazzarino, M.C.10
Candido, S.11
Libra, M.12
Basecke, J.13
-
38
-
-
84876988997
-
Everolimus vs. temsirolimus for advanced renal cell carcinoma: use and use of resources in the US Oncology Network
-
Vogelzang NJ, Bhor M, Liu Z, Dhanda R, Hutson TE. Everolimus vs. temsirolimus for advanced renal cell carcinoma: use and use of resources in the US Oncology Network. Clin Genitourin Cancer. 2013; 11:115-120.
-
(2013)
Clin Genitourin Cancer
, vol.11
, pp. 115-120
-
-
Vogelzang, N.J.1
Bhor, M.2
Liu, Z.3
Dhanda, R.4
Hutson, T.E.5
-
39
-
-
84863078767
-
Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer
-
Baselga J, Campone M, Piccart M, Burris HA, III, Rugo HS, Sahmoud T, Noguchi S, Gnant M, Pritchard KI, Lebrun F, Beck JT, Ito Y, Yardley D, et al. Everolimus in postmenopausal hormone-receptor-positive advanced breast cancer. N Engl J Med. 2012; 366:520-529.
-
(2012)
N Engl J Med
, vol.366
, pp. 520-529
-
-
Baselga, J.1
Campone, M.2
Piccart, M.3
Burris, H.A.4
Rugo, H.S.5
Sahmoud, T.6
Noguchi, S.7
Gnant, M.8
Pritchard, K.I.9
Lebrun, F.10
Beck, J.T.11
Ito, Y.12
Yardley, D.13
-
40
-
-
51349164790
-
Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer
-
Carracedo A, Ma L, Teruya-Feldstein J, Rojo F, Salmena L, Alimonti A, Egia A, Sasaki AT, Thomas G, Kozma SC, Papa A, Nardella C, Cantley LC, et al. Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer. J Clin Invest. 2008; 118:3065-3074.
-
(2008)
J Clin Invest
, vol.118
, pp. 3065-3074
-
-
Carracedo, A.1
Ma, L.2
Teruya-Feldstein, J.3
Rojo, F.4
Salmena, L.5
Alimonti, A.6
Egia, A.7
Sasaki, A.T.8
Thomas, G.9
Kozma, S.C.10
Papa, A.11
Nardella, C.12
Cantley, L.C.13
-
41
-
-
84857417355
-
Feedback upregulation of HER3 (ErbB3) expression and activity attenuates antitumor effect of PI3K inhibitors
-
Chakrabarty A, Sanchez V, Kuba MG, Rinehart C, Arteaga CL. Feedback upregulation of HER3 (ErbB3) expression and activity attenuates antitumor effect of PI3K inhibitors. Proc Natl Acad Sci USA. 2012; 109:2718-2723.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 2718-2723
-
-
Chakrabarty, A.1
Sanchez, V.2
Kuba, M.G.3
Rinehart, C.4
Arteaga, C.L.5
-
42
-
-
79957917078
-
PI3K inhibition results in enhanced HER signaling and acquired ERK dependency in HER2-overexpressing breast cancer
-
Serra V, Scaltriti M, Prudkin L, Eichhorn PJ, Ibrahim YH, Chandarlapaty S, Markman B, Rodriguez O, Guzman M, Rodriguez S, Gili M, Russillo M, Parra JL, et al. PI3K inhibition results in enhanced HER signaling and acquired ERK dependency in HER2-overexpressing breast cancer. Oncogene. 2011; 30:2547-2557.
-
(2011)
Oncogene
, vol.30
, pp. 2547-2557
-
-
Serra, V.1
Scaltriti, M.2
Prudkin, L.3
Eichhorn, P.J.4
Ibrahim, Y.H.5
Chandarlapaty, S.6
Markman, B.7
Rodriguez, O.8
Guzman, M.9
Rodriguez, S.10
Gili, M.11
Russillo, M.12
Parra, J.L.13
-
43
-
-
51049109033
-
Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity
-
Maira SM, Stauffer F, Brueggen J, Furet P, Schnell C, Fritsch C, Brachmann S, Chene P, De PA, Schoemaker K, Fabbro D, Gabriel D, Simonen M, et al. Identification and characterization of NVP-BEZ235, a new orally available dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor with potent in vivo antitumor activity. Mol Cancer Ther. 2008; 7:1851-1863.
-
(2008)
Mol Cancer Ther
, vol.7
, pp. 1851-1863
-
-
Maira, S.M.1
Stauffer, F.2
Brueggen, J.3
Furet, P.4
Schnell, C.5
Fritsch, C.6
Brachmann, S.7
Chene, P.8
De, P.A.9
Schoemaker, K.10
Fabbro, D.11
Gabriel, D.12
Simonen, M.13
-
44
-
-
84904622446
-
Phase I study of PF-04691502, a small-molecule, oral, dual inhibitor of PI3K and mTOR, in patients with advanced cancer.[Erratum appears in Invest New Drug. 2014 Jun; 32(3):575]
-
Britten CD, Adjei AA, Millham R, Houk BE, Borzillo G, Pierce K, Wainberg ZA, Lorusso PM. Phase I study of PF-04691502, a small-molecule, oral, dual inhibitor of PI3K and mTOR, in patients with advanced cancer.[Erratum appears in Invest New Drugs. 2014 Jun; 32(3):575]. Invest New Drugs. 2014; 32:510-517.
-
(2014)
Invest New Drugs
, vol.32
, pp. 510-517
-
-
Britten, C.D.1
Adjei, A.A.2
Millham, R.3
Houk, B.E.4
Borzillo, G.5
Pierce, K.6
Wainberg, Z.A.7
Lorusso, P.M.8
-
45
-
-
79955996030
-
Antitumor efficacy of PKI-587, a highly potent dual PI3K/mTOR kinase inhibitor
-
Mallon R, Feldberg LR, Lucas J, Chaudhary I, Dehnhardt C, Santos ED, Chen Z, dos SO, Ayral-Kaloustian S, Venkatesan A, Hollander I. Antitumor efficacy of PKI-587, a highly potent dual PI3K/mTOR kinase inhibitor. Clini Cancer Res. 2011; 17:3193-3203.
-
(2011)
Clini Cancer Res
, vol.17
, pp. 3193-3203
-
-
Mallon, R.1
Feldberg, L.R.2
Lucas, J.3
Chaudhary, I.4
Dehnhardt, C.5
Santos, E.D.6
Chen, Z.7
dos, S.O.8
Ayral-Kaloustian, S.9
Venkatesan, A.10
Hollander, I.11
-
46
-
-
80455140538
-
Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer
-
Sutherlin DP, Bao L, Berry M, Castanedo G, Chuckowree I, Dotson J, Folks A, Friedman L, Goldsmith R, Gunzner J, Heffron T, Lesnick J, Lewis C, et al. Discovery of a potent, selective, and orally available class I phosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) kinase inhibitor (GDC-0980) for the treatment of cancer. J Med Chem. 2011; 54:7579-7587.
-
(2011)
J Med Chem
, vol.54
, pp. 7579-7587
-
-
Sutherlin, D.P.1
Bao, L.2
Berry, M.3
Castanedo, G.4
Chuckowree, I.5
Dotson, J.6
Folks, A.7
Friedman, L.8
Goldsmith, R.9
Gunzner, J.10
Heffron, T.11
Lesnick, J.12
Lewis, C.13
-
47
-
-
77954638677
-
Discovery of GSK2126458, a Highly Potent Inhibitor of PI3K and the Mammalian Target of Rapamycin
-
Knight SD, Adams ND, Burgess JL, Chaudhari AM, Darcy MG, Donatelli CA, Luengo JI, Newlander KA, Parrish CA, Ridgers LH, Sarpong MA, Schmidt SJ, Van Aller GS, et al. Discovery of GSK2126458, a Highly Potent Inhibitor of PI3K and the Mammalian Target of Rapamycin. ACS Med Chem Lett. 2010; 1:39-43.
-
(2010)
ACS Med Chem Lett
, vol.1
, pp. 39-43
-
-
Knight, S.D.1
Adams, N.D.2
Burgess, J.L.3
Chaudhari, A.M.4
Darcy, M.G.5
Donatelli, C.A.6
Luengo, J.I.7
Newlander, K.A.8
Parrish, C.A.9
Ridgers, L.H.10
Sarpong, M.A.11
Schmidt, S.J.12
Van Aller, G.S.13
-
48
-
-
84904720579
-
Thioredoxin and glutaredoxinmediated redox regulation of ribonucleotide reductase
-
Sengupta R, Holmgren A. Thioredoxin and glutaredoxinmediated redox regulation of ribonucleotide reductase. World J Biolog Chem. 2014; 5:68-74.
-
(2014)
World J Biolog Chem
, vol.5
, pp. 68-74
-
-
Sengupta, R.1
Holmgren, A.2
-
49
-
-
0026715172
-
Thioredoxin regulates the DNA binding activity of NF-kappa B by reduction of a disulphide bond involving cysteine 62
-
Matthews JR, Wakasugi N, Virelizier JL, Yodoi J, Hay RT. Thioredoxin regulates the DNA binding activity of NF-kappa B by reduction of a disulphide bond involving cysteine 62. Nucleic Acids Res. 1992; 20:3821-3830.
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 3821-3830
-
-
Matthews, J.R.1
Wakasugi, N.2
Virelizier, J.L.3
Yodoi, J.4
Hay, R.T.5
-
50
-
-
0033544915
-
Thioredoxin-dependent redox regulation of p53-mediated p21 activation
-
Ueno M, Masutani H, Arai RJ, Yamauchi A, Hirota K, Sakai T, Inamoto T, Yamaoka Y, Yodoi J, Nikaido T. Thioredoxin-dependent redox regulation of p53-mediated p21 activation. J Biolog Chem. 1999; 274:35809-35815.
-
(1999)
J Biolog Chem
, vol.274
, pp. 35809-35815
-
-
Ueno, M.1
Masutani, H.2
Arai, R.J.3
Yamauchi, A.4
Hirota, K.5
Sakai, T.6
Inamoto, T.7
Yamaoka, Y.8
Yodoi, J.9
Nikaido, T.10
-
51
-
-
0029753008
-
Activation of hypoxia-inducible transcription factor depends primarily upon redox-sensitive stabilization of its alpha subunit
-
Huang LE, Arany Z, Livingston DM, Bunn HF. Activation of hypoxia-inducible transcription factor depends primarily upon redox-sensitive stabilization of its alpha subunit. J Biol Chem. 1996; 271:32253-32259.
-
(1996)
J Biol Chem
, vol.271
, pp. 32253-32259
-
-
Huang, L.E.1
Arany, Z.2
Livingston, D.M.3
Bunn, H.F.4
-
52
-
-
33644818614
-
Thioredoxin catalyzes the S-nitrosation of the caspase-3 active site cysteine
-
Mitchell DA, Marletta MA. Thioredoxin catalyzes the S-nitrosation of the caspase-3 active site cysteine. Nat Chem Biol. 2005; 1:154-158.
-
(2005)
Nat Chem Biol
, vol.1
, pp. 154-158
-
-
Mitchell, D.A.1
Marletta, M.A.2
-
53
-
-
44449119080
-
Regulated protein denitrosylation by cytosolic and mitochondrial thioredoxins
-
Benhar M, Forrester MT, Hess DT, Stamler JS. Regulated protein denitrosylation by cytosolic and mitochondrial thioredoxins. Science. 2008; 320:1050-1054.
-
(2008)
Science
, vol.320
, pp. 1050-1054
-
-
Benhar, M.1
Forrester, M.T.2
Hess, D.T.3
Stamler, J.S.4
-
54
-
-
55249106018
-
The thiol redox state of lymphoid organs is modified by immunization: role of different immune cell populations
-
Castellani P, Angelini G, Delfino L, Matucci A, Rubartelli A. The thiol redox state of lymphoid organs is modified by immunization: role of different immune cell populations. Eur J Immunol. 2008; 38:2419-2425.
-
(2008)
Eur J Immunol
, vol.38
, pp. 2419-2425
-
-
Castellani, P.1
Angelini, G.2
Delfino, L.3
Matucci, A.4
Rubartelli, A.5
-
55
-
-
84862796550
-
Antitumor activity of a novel STAT3 inhibitor and redox modulator in non-small cell lung cancer cells
-
Liu X, Guo W, Wu S, Wang L, Wang J, Dai B, Kim ES, Heymach JV, Wang M, Girard L, Minna J, Roth JA, Swisher SG, et al. Antitumor activity of a novel STAT3 inhibitor and redox modulator in non-small cell lung cancer cells. Biochem Pharmacol. 2012; 83:1456-1464.
-
(2012)
Biochem Pharmacol
, vol.83
, pp. 1456-1464
-
-
Liu, X.1
Guo, W.2
Wu, S.3
Wang, L.4
Wang, J.5
Dai, B.6
Kim, E.S.7
Heymach, J.V.8
Wang, M.9
Girard, L.10
Minna, J.11
Roth, J.A.12
Swisher, S.G.13
-
56
-
-
0037364872
-
Comparison of the sulforhodamine B assay and the clonogenic assay for in vitro chemoradiation studies
-
Pauwels B, Korst AE, de Pooter CM, Pattyn GG, Lambrechts HA, Baay MF, Lardon F, Vermorken JB. Comparison of the sulforhodamine B assay and the clonogenic assay for in vitro chemoradiation studies. Cancer Chemother Pharmacol. 2003; 51:221-226.
-
(2003)
Cancer Chemother Pharmacol
, vol.51
, pp. 221-226
-
-
Pauwels, B.1
Korst, A.E.2
de Pooter, C.M.3
Pattyn, G.G.4
Lambrechts, H.A.5
Baay, M.F.6
Lardon, F.7
Vermorken, J.B.8
-
57
-
-
84921365300
-
Expression of sulfotransferase SULT1A1 in cancer cells predicts susceptibility to the novel anticancer agent NSC-743380
-
Huang X, Cao M, Wang L, Wu S, Liu X, Li H, Zhang H, Wang RY, Sun X, Wei C, Baggerly KA, Roth JA, Wang M, et al. Expression of sulfotransferase SULT1A1 in cancer cells predicts susceptibility to the novel anticancer agent NSC-743380. Oncotarget. 2015; 6:345-354. doi: 10.18632/oncotarget.2814.
-
(2015)
Oncotarget
, vol.6
, pp. 345-354
-
-
Huang, X.1
Cao, M.2
Wang, L.3
Wu, S.4
Liu, X.5
Li, H.6
Zhang, H.7
Wang, R.Y.8
Sun, X.9
Wei, C.10
Baggerly, K.A.11
Roth, J.A.12
Wang, M.13
-
58
-
-
34548141874
-
Non-parametric quantification of protein lysate arrays
-
Hu J, He X, Baggerly KA, Coombes KR, Hennessy BT, Mills GB. Non-parametric quantification of protein lysate arrays. Bioinformatics. 2007; 23:1986-1994.
-
(2007)
Bioinformatics
, vol.23
, pp. 1986-1994
-
-
Hu, J.1
He, X.2
Baggerly, K.A.3
Coombes, K.R.4
Hennessy, B.T.5
Mills, G.B.6
|