-
1
-
-
0009682267
-
Prodrugs in cancer chemotherapy
-
Knox R.J., Connors T.A. Prodrugs in cancer chemotherapy. Pathol. Oncol. Res. 1997, 3(4):309-324.
-
(1997)
Pathol. Oncol. Res.
, vol.3
, Issue.4
, pp. 309-324
-
-
Knox, R.J.1
Connors, T.A.2
-
2
-
-
0035415493
-
Prodrug strategies in cancer therapy
-
Denny W.A. Prodrug strategies in cancer therapy. Eur. J. Med. Chem. 2001, 36(7-8):577-595.
-
(2001)
Eur. J. Med. Chem.
, vol.36
, Issue.7-8
, pp. 577-595
-
-
Denny, W.A.1
-
3
-
-
40149088986
-
Prodrugs: design and clinical applications
-
Rautio J., et al. Prodrugs: design and clinical applications. Nat. Rev. Drug Discov. 2008, 7(3):255-270.
-
(2008)
Nat. Rev. Drug Discov.
, vol.7
, Issue.3
, pp. 255-270
-
-
Rautio, J.1
-
4
-
-
52049105453
-
Recent trends in targeted anticancer prodrug and conjugate design
-
Singh Y., Palombo M., Sinko P.J. Recent trends in targeted anticancer prodrug and conjugate design. Curr. Med. Chem. 2008, 15(18):1802-1826.
-
(2008)
Curr. Med. Chem.
, vol.15
, Issue.18
, pp. 1802-1826
-
-
Singh, Y.1
Palombo, M.2
Sinko, P.J.3
-
5
-
-
72449187503
-
Prodrug approaches for enhancing the bioavailability of drugs with low solubility
-
Muller C.E. Prodrug approaches for enhancing the bioavailability of drugs with low solubility. Chem. Biodivers. 2009, 6(11):2071-2083.
-
(2009)
Chem. Biodivers.
, vol.6
, Issue.11
, pp. 2071-2083
-
-
Muller, C.E.1
-
6
-
-
0042143281
-
Targeted prodrug design to optimize drug delivery
-
Han H.K., Amidon G.L. Targeted prodrug design to optimize drug delivery. AAPS PharmSci 2000, 2(1):E6.
-
(2000)
AAPS PharmSci
, vol.2
, Issue.1
-
-
Han, H.K.1
Amidon, G.L.2
-
7
-
-
33745031316
-
Enzymes involved in the bioconversion of ester-based prodrugs
-
Liederer B.M., Borchardt R.T. Enzymes involved in the bioconversion of ester-based prodrugs. J. Pharm. Sci. 2006, 95(6):1177-1195.
-
(2006)
J. Pharm. Sci.
, vol.95
, Issue.6
, pp. 1177-1195
-
-
Liederer, B.M.1
Borchardt, R.T.2
-
8
-
-
0036827812
-
In vitro stability and in vivo pharmacokinetic studies of a model opioid peptide, H-Tyr-D-Ala-Gly-Phe-D-Leu-OH (DADLE), and its cyclic prodrugs
-
Yang J.Z., Chen W., Borchardt R.T. In vitro stability and in vivo pharmacokinetic studies of a model opioid peptide, H-Tyr-D-Ala-Gly-Phe-D-Leu-OH (DADLE), and its cyclic prodrugs. J. Pharmacol. Exp. Ther. 2002, 303(2):840-848.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.303
, Issue.2
, pp. 840-848
-
-
Yang, J.Z.1
Chen, W.2
Borchardt, R.T.3
-
9
-
-
42249108725
-
DTS-108, a novel peptidic prodrug of SN38: in vivo efficacy and toxicokinetic studies
-
Meyer-Losic F., et al. DTS-108, a novel peptidic prodrug of SN38: in vivo efficacy and toxicokinetic studies. Clin. Cancer Res. 2008, 14(7):2145-2153.
-
(2008)
Clin. Cancer Res.
, vol.14
, Issue.7
, pp. 2145-2153
-
-
Meyer-Losic, F.1
-
10
-
-
70349988803
-
PEG conjugates in clinical development or use as anticancer agents: an overview
-
Pasut G., Veronese F.M. PEG conjugates in clinical development or use as anticancer agents: an overview. Adv. Drug Deliv. Rev. 2009, 61(13):1177-1188.
-
(2009)
Adv. Drug Deliv. Rev.
, vol.61
, Issue.13
, pp. 1177-1188
-
-
Pasut, G.1
Veronese, F.M.2
-
11
-
-
0141458033
-
Synthesis of linear, beta-cyclodextrin-based polymers and their camptothecin conjugates
-
Cheng J., et al. Synthesis of linear, beta-cyclodextrin-based polymers and their camptothecin conjugates. Bioconjug. Chem. 2003, 14(5):1007-1017.
-
(2003)
Bioconjug. Chem.
, vol.14
, Issue.5
, pp. 1007-1017
-
-
Cheng, J.1
-
12
-
-
70349992906
-
Design and development of IT-101, a cyclodextrin-containing polymer conjugate of camptothecin
-
Davis M.E. Design and development of IT-101, a cyclodextrin-containing polymer conjugate of camptothecin. Adv. Drug Deliv. Rev. 2009, 61(13):1189-1192.
-
(2009)
Adv. Drug Deliv. Rev.
, vol.61
, Issue.13
, pp. 1189-1192
-
-
Davis, M.E.1
-
13
-
-
42749091133
-
Polymer-drug conjugates: recent development in clinical oncology
-
Li C., Wallace S. Polymer-drug conjugates: recent development in clinical oncology. Adv. Drug Deliv. Rev. 2008, 60(8):886-898.
-
(2008)
Adv. Drug Deliv. Rev.
, vol.60
, Issue.8
, pp. 886-898
-
-
Li, C.1
Wallace, S.2
-
14
-
-
0033678680
-
A peptide-doxorubicin 'prodrug' activated by prostate-specific antigen selectively kills prostate tumor cells positive for prostate-specific antigen in vivo
-
DeFeo-Jones D., et al. A peptide-doxorubicin 'prodrug' activated by prostate-specific antigen selectively kills prostate tumor cells positive for prostate-specific antigen in vivo. Nat. Med. 2000, 6(11):1248-1252.
-
(2000)
Nat. Med.
, vol.6
, Issue.11
, pp. 1248-1252
-
-
DeFeo-Jones, D.1
-
15
-
-
45749145876
-
Evaluation of ketone-oxime method for developing therapeutic on-demand cleavable immunoconjugates
-
Kumaresan P.R., et al. Evaluation of ketone-oxime method for developing therapeutic on-demand cleavable immunoconjugates. Bioconjug. Chem. 2008, 19(6):1313-1318.
-
(2008)
Bioconjug. Chem.
, vol.19
, Issue.6
, pp. 1313-1318
-
-
Kumaresan, P.R.1
-
16
-
-
33645891179
-
Enhanced hepatic uptake and bioactivity of type alpha1(I) collagen gene promoter-specific triplex-forming oligonucleotides after conjugation with cholesterol
-
Cheng K., et al. Enhanced hepatic uptake and bioactivity of type alpha1(I) collagen gene promoter-specific triplex-forming oligonucleotides after conjugation with cholesterol. J. Pharmacol. Exp. Ther. 2006, 317(2):797-805.
-
(2006)
J. Pharmacol. Exp. Ther.
, vol.317
, Issue.2
, pp. 797-805
-
-
Cheng, K.1
-
17
-
-
56449129810
-
Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate
-
Lewis Phillips G.D., et al. Targeting HER2-positive breast cancer with trastuzumab-DM1, an antibody-cytotoxic drug conjugate. Cancer Res. 2008, 68(22):9280-9290.
-
(2008)
Cancer Res.
, vol.68
, Issue.22
, pp. 9280-9290
-
-
Lewis Phillips, G.D.1
-
18
-
-
67649886201
-
Potent antibody drug conjugates for cancer therapy
-
Senter P.D. Potent antibody drug conjugates for cancer therapy. Curr. Opin. Chem. Biol. 2009, 13(3):235-244.
-
(2009)
Curr. Opin. Chem. Biol.
, vol.13
, Issue.3
, pp. 235-244
-
-
Senter, P.D.1
-
19
-
-
55249097877
-
Novel peptide linkers for highly potent antibody-auristatin conjugate
-
Doronina S.O., et al. Novel peptide linkers for highly potent antibody-auristatin conjugate. Bioconjug. Chem. 2008, 19(10):1960-1963.
-
(2008)
Bioconjug. Chem.
, vol.19
, Issue.10
, pp. 1960-1963
-
-
Doronina, S.O.1
-
20
-
-
22844436226
-
Recent advances in tumor-targeting anticancer drug conjugates
-
Jaracz S., et al. Recent advances in tumor-targeting anticancer drug conjugates. Bioorg. Med. Chem. 2005, 13(17):5043-5054.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, Issue.17
, pp. 5043-5054
-
-
Jaracz, S.1
-
21
-
-
0035904966
-
Targeted drug conjugates: principles and progress
-
Garnett M.C. Targeted drug conjugates: principles and progress. Adv. Drug Deliv. Rev. 2001, 53(2):171-216.
-
(2001)
Adv. Drug Deliv. Rev.
, vol.53
, Issue.2
, pp. 171-216
-
-
Garnett, M.C.1
-
23
-
-
0033870271
-
Oncotic pressure in solid tumors is elevated
-
Stohrer M., et al. Oncotic pressure in solid tumors is elevated. Cancer Res. 2000, 60(15):4251-4255.
-
(2000)
Cancer Res.
, vol.60
, Issue.15
, pp. 4251-4255
-
-
Stohrer, M.1
-
24
-
-
0032006660
-
Increased affinity leads to improved selective tumor delivery of single-chain Fv antibodies
-
Adams G.P., et al. Increased affinity leads to improved selective tumor delivery of single-chain Fv antibodies. Cancer Res. 1998, 58(3):485-490.
-
(1998)
Cancer Res.
, vol.58
, Issue.3
, pp. 485-490
-
-
Adams, G.P.1
-
25
-
-
74849092615
-
Antibody-drug conjugate targets
-
Teicher B.A. Antibody-drug conjugate targets. Curr. Cancer Drug Targets 2009, 9(8):982-1004.
-
(2009)
Curr. Cancer Drug Targets
, vol.9
, Issue.8
, pp. 982-1004
-
-
Teicher, B.A.1
-
27
-
-
69249109709
-
PSMA expression in Schwannoma: a potential clinical mimicker of metastatic prostate carcinoma
-
Wang W., et al. PSMA expression in Schwannoma: a potential clinical mimicker of metastatic prostate carcinoma. Urol. Oncol. 2009, 27(5):525-528.
-
(2009)
Urol. Oncol.
, vol.27
, Issue.5
, pp. 525-528
-
-
Wang, W.1
-
28
-
-
0023519561
-
Disposition of the monoclonal antibody-vinca alkaloid conjugate, KS1/4-DAVLB (LY256787), in Fischer 344 rats and rhesus monkeys
-
Spearman M.E., Goodwin R.M., Kau D. Disposition of the monoclonal antibody-vinca alkaloid conjugate, KS1/4-DAVLB (LY256787), in Fischer 344 rats and rhesus monkeys. Drug Metab. Dispos. 1987, 15(5):640-647.
-
(1987)
Drug Metab. Dispos.
, vol.15
, Issue.5
, pp. 640-647
-
-
Spearman, M.E.1
Goodwin, R.M.2
Kau, D.3
-
29
-
-
77249172711
-
Synthesis and preliminary biological evaluation of high-drug-load paclitaxel-antibody conjugates for tumor-targeted chemotherapy
-
Quiles S., et al. Synthesis and preliminary biological evaluation of high-drug-load paclitaxel-antibody conjugates for tumor-targeted chemotherapy. J. Med. Chem. 2010, 53(2):586-594.
-
(2010)
J. Med. Chem.
, vol.53
, Issue.2
, pp. 586-594
-
-
Quiles, S.1
-
30
-
-
20144375952
-
An anti-MUC1 antibody-calicheamicin conjugate for treatment of solid tumors. Choice of linker and overcoming drug resistance
-
Hamann P.R., et al. An anti-MUC1 antibody-calicheamicin conjugate for treatment of solid tumors. Choice of linker and overcoming drug resistance. Bioconjug. Chem. 2005, 16(2):346-353.
-
(2005)
Bioconjug. Chem.
, vol.16
, Issue.2
, pp. 346-353
-
-
Hamann, P.R.1
-
31
-
-
38749090101
-
The oncofetal protein, 5T4, is a suitable target for antibody-guided anti-cancer chemotherapy with calicheamicin
-
Boghaert E.R., et al. The oncofetal protein, 5T4, is a suitable target for antibody-guided anti-cancer chemotherapy with calicheamicin. Int. J. Oncol. 2008, 32(1):221-234.
-
(2008)
Int. J. Oncol.
, vol.32
, Issue.1
, pp. 221-234
-
-
Boghaert, E.R.1
-
32
-
-
77954031486
-
Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3weeks to patients with HER2-positive metastatic breast cancer
-
Krop I.E., et al. Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3weeks to patients with HER2-positive metastatic breast cancer. J. Clin. Oncol. 2010, 28(16):2698-2704.
-
(2010)
J. Clin. Oncol.
, vol.28
, Issue.16
, pp. 2698-2704
-
-
Krop, I.E.1
-
33
-
-
0038351870
-
Antibody-targeted chemotherapy of acute myeloid leukemia using gemtuzumab ozogamicin (Mylotarg)
-
Sievers E.L. Antibody-targeted chemotherapy of acute myeloid leukemia using gemtuzumab ozogamicin (Mylotarg). Blood Cells Mol. Dis. 2003, 31(1):7-10.
-
(2003)
Blood Cells Mol. Dis.
, vol.31
, Issue.1
, pp. 7-10
-
-
Sievers, E.L.1
-
34
-
-
0035874504
-
Targeting of the CD33-calicheamicin immunoconjugate Mylotarg (CMA-676) in acute myeloid leukemia: in vivo and in vitro saturation and internalization by leukemic and normal myeloid cells
-
van Der Velden V.H., et al. Targeting of the CD33-calicheamicin immunoconjugate Mylotarg (CMA-676) in acute myeloid leukemia: in vivo and in vitro saturation and internalization by leukemic and normal myeloid cells. Blood 2001, 97(10):3197-3204.
-
(2001)
Blood
, vol.97
, Issue.10
, pp. 3197-3204
-
-
van Der Velden, V.H.1
-
35
-
-
3242749618
-
Pharmacokinetics of gemtuzumab ozogamicin as a single-agent treatment of pediatric patients with refractory or relapsed acute myeloid leukemia
-
Buckwalter M., et al. Pharmacokinetics of gemtuzumab ozogamicin as a single-agent treatment of pediatric patients with refractory or relapsed acute myeloid leukemia. J. Clin. Pharmacol. 2004, 44(8):873-880.
-
(2004)
J. Clin. Pharmacol.
, vol.44
, Issue.8
, pp. 873-880
-
-
Buckwalter, M.1
-
36
-
-
84870712457
-
-
cited; Available from:
-
Mylotarg (gemtuzumab ozogamicin): Market Withdrawal cited; Available from:. http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm216458.htm.
-
Mylotarg (gemtuzumab ozogamicin): Market Withdrawal
-
-
-
37
-
-
78651447411
-
A phase 2 study of trastuzumab-dm 1 (t-dm 1), a novel her 2 antibody-drug conjugate, in her 2+ metastatic breast cancer (mbc) patients previously treated with conventional chemotherapy, lapatinib and trastuzumab
-
Krop I., et al. A phase 2 study of trastuzumab-dm 1 (t-dm 1), a novel her 2 antibody-drug conjugate, in her 2+ metastatic breast cancer (mbc) patients previously treated with conventional chemotherapy, lapatinib and trastuzumab. San Antonio Brest Cancer Symposium 2009.
-
(2009)
San Antonio Brest Cancer Symposium
-
-
Krop, I.1
-
38
-
-
31544455876
-
Antitumor efficacy of a combination of CMC-544 (inotuzumab ozogamicin), a CD22-targeted cytotoxic immunoconjugate of calicheamicin, and rituximab against non-Hodgkin's B-cell lymphoma
-
DiJoseph J.F., et al. Antitumor efficacy of a combination of CMC-544 (inotuzumab ozogamicin), a CD22-targeted cytotoxic immunoconjugate of calicheamicin, and rituximab against non-Hodgkin's B-cell lymphoma. Clin. Cancer Res. 2006, 12(1):242-249.
-
(2006)
Clin. Cancer Res.
, vol.12
, Issue.1
, pp. 242-249
-
-
DiJoseph, J.F.1
-
39
-
-
77956292811
-
The role of HER2 in cancer therapy and targeted drug delivery
-
Tai W., Mahato R., Cheng K., et al. The role of HER2 in cancer therapy and targeted drug delivery. J. Control. Release 2010, 146(3):264-275.
-
(2010)
J. Control. Release
, vol.146
, Issue.3
, pp. 264-275
-
-
Tai, W.1
Mahato, R.2
Cheng, K.3
-
40
-
-
77954031486
-
Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3weeks to patients with HER2-positive metastatic breast cancer
-
Krop I.E., et al. Phase I study of trastuzumab-DM1, an HER2 antibody-drug conjugate, given every 3weeks to patients with HER2-positive metastatic breast cancer. J. Clin. Oncol. 2010, 28(16):2698-2704.
-
(2010)
J. Clin. Oncol.
, vol.28
, Issue.16
, pp. 2698-2704
-
-
Krop, I.E.1
-
41
-
-
79959949642
-
Preliminary report of a phase 1 study of CMC-544, an antibody-targeted chemotherapy agent, in patients with B-cell non-Hodgkin's lymphoma (NHL)
-
Advani Anjali, E.G.*, Gisselbrecht Christian, Rohatiner Ama, Rosen Steven, Smith Mitchell, Boni* Joseph, Lejeune* Chantal, Patel Hemant Preliminary report of a phase 1 study of CMC-544, an antibody-targeted chemotherapy agent, in patients with B-cell non-Hodgkin's lymphoma (NHL). American Society of Hematology Annual Meeting 2005.
-
(2005)
American Society of Hematology Annual Meeting
-
-
Advani A.E.G.*1
Gisselbrecht, C.2
Rohatiner, A.3
Rosen, S.4
Smith, M.5
Boni*, J.6
Lejeune*, C.7
Patel, H.8
-
42
-
-
33646768989
-
Novel polymeric prodrug with multivalent components for cancer therapy
-
Khandare J.J., et al. Novel polymeric prodrug with multivalent components for cancer therapy. J. Pharmacol. Exp. Ther. 2006, 317(3):929-937.
-
(2006)
J. Pharmacol. Exp. Ther.
, vol.317
, Issue.3
, pp. 929-937
-
-
Khandare, J.J.1
-
43
-
-
24644496584
-
Tumor-specific targeting of an anticancer drug delivery system by LHRH peptide
-
Dharap S.S., et al. Tumor-specific targeting of an anticancer drug delivery system by LHRH peptide. Proc. Natl Acad. Sci. USA 2005, 102(36):12962-12967.
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, Issue.36
, pp. 12962-12967
-
-
Dharap, S.S.1
-
44
-
-
13944278751
-
Synthesis and biological evaluation of dimeric RGD peptide-paclitaxel conjugate as a model for integrin-targeted drug delivery
-
Chen X., et al. Synthesis and biological evaluation of dimeric RGD peptide-paclitaxel conjugate as a model for integrin-targeted drug delivery. J. Med. Chem. 2005, 48(4):1098-1106.
-
(2005)
J. Med. Chem.
, vol.48
, Issue.4
, pp. 1098-1106
-
-
Chen, X.1
-
45
-
-
39849094180
-
A cell-penetrating peptidic GRP78 ligand for tumor cell-specific prodrug therapy
-
Yoneda Y., et al. A cell-penetrating peptidic GRP78 ligand for tumor cell-specific prodrug therapy. Bioorg. Med. Chem. Lett. 2008, 18(5):1632-1636.
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, Issue.5
, pp. 1632-1636
-
-
Yoneda, Y.1
-
46
-
-
0037470247
-
Global profiling of the cell surface proteome of cancer cells uncovers an abundance of proteins with chaperone function
-
Shin B.K., et al. Global profiling of the cell surface proteome of cancer cells uncovers an abundance of proteins with chaperone function. J. Biol. Chem. 2003, 278(9):7607-7616.
-
(2003)
J. Biol. Chem.
, vol.278
, Issue.9
, pp. 7607-7616
-
-
Shin, B.K.1
-
47
-
-
0032402354
-
Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin
-
Dubowchik G.M., Firestone R.A. Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin. Bioorg. Med. Chem. Lett. 1998, 8(23):3341-3346.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, Issue.23
, pp. 3341-3346
-
-
Dubowchik, G.M.1
Firestone, R.A.2
-
49
-
-
66249129385
-
Selection, characterization and application of new RNA HIV gp 120 aptamers for facile delivery of Dicer substrate siRNAs into HIV infected cells
-
Zhou J., et al. Selection, characterization and application of new RNA HIV gp 120 aptamers for facile delivery of Dicer substrate siRNAs into HIV infected cells. Nucleic Acids Res. 2009, 37(9):3094-3109.
-
(2009)
Nucleic Acids Res.
, vol.37
, Issue.9
, pp. 3094-3109
-
-
Zhou, J.1
-
50
-
-
77956682609
-
Development of DNA aptamers using Cell-SELEX
-
Sefah K., et al. Development of DNA aptamers using Cell-SELEX. Nat. Protoc. 2010, 5(6):1169-1185.
-
(2010)
Nat. Protoc.
, vol.5
, Issue.6
, pp. 1169-1185
-
-
Sefah, K.1
-
51
-
-
33745128099
-
Aptamer mediated siRNA delivery
-
Chu T.C., et al. Aptamer mediated siRNA delivery. Nucleic Acids Res. 2006, 34(10):e73.
-
(2006)
Nucleic Acids Res.
, vol.34
, Issue.10
-
-
Chu, T.C.1
-
52
-
-
7444223607
-
Nanoparticle-aptamer bioconjugates: a new approach for targeting prostate cancer cells
-
Farokhzad O.C., et al. Nanoparticle-aptamer bioconjugates: a new approach for targeting prostate cancer cells. Cancer Res. 2004, 64(21):7668-7672.
-
(2004)
Cancer Res.
, vol.64
, Issue.21
, pp. 7668-7672
-
-
Farokhzad, O.C.1
-
53
-
-
34249101981
-
Phase I evaluation of J591 as a vascular targeting agent in progressive solid tumors
-
Morris M.J., et al. Phase I evaluation of J591 as a vascular targeting agent in progressive solid tumors. Clin. Cancer Res. 2007, 13(9):2707-2713.
-
(2007)
Clin. Cancer Res.
, vol.13
, Issue.9
, pp. 2707-2713
-
-
Morris, M.J.1
-
54
-
-
33947529429
-
Vascular targeted therapy with anti-prostate-specific membrane antigen monoclonal antibody J591 in advanced solid tumors
-
Milowsky M.I., et al. Vascular targeted therapy with anti-prostate-specific membrane antigen monoclonal antibody J591 in advanced solid tumors. J. Clin. Oncol. 2007, 25(5):540-547.
-
(2007)
J. Clin. Oncol.
, vol.25
, Issue.5
, pp. 540-547
-
-
Milowsky, M.I.1
-
55
-
-
56249097260
-
Targeted delivery of cisplatin to prostate cancer cells by aptamer functionalized Pt(IV) prodrug-PLGA-PEG nanoparticles
-
Dhar S., et al. Targeted delivery of cisplatin to prostate cancer cells by aptamer functionalized Pt(IV) prodrug-PLGA-PEG nanoparticles. Proc. Natl Acad. Sci. USA 2008, 105(45):17356-17361.
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, Issue.45
, pp. 17356-17361
-
-
Dhar, S.1
-
56
-
-
78149260773
-
Engineering of self-assembled nanoparticle platform for precisely controlled combination drug therapy
-
Kolishetti N., et al. Engineering of self-assembled nanoparticle platform for precisely controlled combination drug therapy. Proc. Natl. Acad. Sci. U. S. A. 2010, 107(42):17939-17944.
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, Issue.42
, pp. 17939-17944
-
-
Kolishetti, N.1
-
57
-
-
65549102827
-
Molecular assembly of an aptamer-drug conjugate for targeted drug delivery to tumor cells
-
Huang Y.F., et al. Molecular assembly of an aptamer-drug conjugate for targeted drug delivery to tumor cells. Chembiochem 2009, 10(5):862-868.
-
(2009)
Chembiochem
, vol.10
, Issue.5
, pp. 862-868
-
-
Huang, Y.F.1
-
58
-
-
33747053632
-
Aptamers evolved from live cells as effective molecular probes for cancer study
-
Shangguan D., et al. Aptamers evolved from live cells as effective molecular probes for cancer study. Proc. Natl Acad. Sci. USA 2006, 103(32):11838-11843.
-
(2006)
Proc. Natl Acad. Sci. USA
, vol.103
, Issue.32
, pp. 11838-11843
-
-
Shangguan, D.1
-
59
-
-
33748294199
-
Synthesis and activity of a folate peptide camptothecin prodrug
-
Henne W.A., et al. Synthesis and activity of a folate peptide camptothecin prodrug. Bioorg. Med. Chem. Lett. 2006, 16(20):5350-5355.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, Issue.20
, pp. 5350-5355
-
-
Henne, W.A.1
-
60
-
-
0038246506
-
Folate-targeted PEG as a potential carrier for carboplatin analogs. Synthesis and in vitro studies
-
Aronov O., et al. Folate-targeted PEG as a potential carrier for carboplatin analogs. Synthesis and in vitro studies. Bioconjug. Chem. 2003, 14(3):563-574.
-
(2003)
Bioconjug. Chem.
, vol.14
, Issue.3
, pp. 563-574
-
-
Aronov, O.1
-
61
-
-
77954764578
-
-
Doxorubicin conjugated to D-alpha-tocopheryl polyethylene glycol succinate and folic acid as a prodrug for targeted chemotherapy.
-
V. Anbharasi, N. Cao, S.S. Feng, Doxorubicin conjugated to D-alpha-tocopheryl polyethylene glycol succinate and folic acid as a prodrug for targeted chemotherapy. J. Biomed. Mater. Res. A. 94(3) 730-743.
-
J. Biomed. Mater. Res. A.
, vol.94
, Issue.3
, pp. 730-743
-
-
Anbharasi, V.1
Cao, N.2
Feng, S.S.3
-
62
-
-
0037404403
-
Targeted disruption of the peptide transporter Pept2 gene in mice defines its physiological role in the kidney
-
Rubio-Aliaga I., et al. Targeted disruption of the peptide transporter Pept2 gene in mice defines its physiological role in the kidney. Mol. Cell. Biol. 2003, 23(9):3247-3252.
-
(2003)
Mol. Cell. Biol.
, vol.23
, Issue.9
, pp. 3247-3252
-
-
Rubio-Aliaga, I.1
-
64
-
-
18044374166
-
Targeted delivery to PEPT1-overexpressing cells: acidic, basic, and secondary floxuridine amino acid ester prodrugs
-
Landowski C.P., et al. Targeted delivery to PEPT1-overexpressing cells: acidic, basic, and secondary floxuridine amino acid ester prodrugs. Mol. Cancer Ther. 2005, 4(4):659-667.
-
(2005)
Mol. Cancer Ther.
, vol.4
, Issue.4
, pp. 659-667
-
-
Landowski, C.P.1
-
65
-
-
0030805221
-
Carrier-mediated transport of oligopeptides in the human fibrosarcoma cell line HT1080
-
Nakanishi T., et al. Carrier-mediated transport of oligopeptides in the human fibrosarcoma cell line HT1080. Cancer Res. 1997, 57(18):4118-4122.
-
(1997)
Cancer Res.
, vol.57
, Issue.18
, pp. 4118-4122
-
-
Nakanishi, T.1
-
66
-
-
0033813664
-
Cancer cell-targeted drug delivery utilizing oligopeptide transport activity
-
Nakanishi T., et al. Cancer cell-targeted drug delivery utilizing oligopeptide transport activity. Int. J. Cancer 2000, 88(2):274-280.
-
(2000)
Int. J. Cancer
, vol.88
, Issue.2
, pp. 274-280
-
-
Nakanishi, T.1
-
67
-
-
79959943206
-
-
XenoPort, Inc., Santa Clare, CA (US): USA
-
Gallop M.A. Gemcitabine Prodrugs, Pharmaceuticals Compositions and Uses Thereof 2010, 1-52. XenoPort, Inc., Santa Clare, CA (US): USA.
-
(2010)
Gemcitabine Prodrugs, Pharmaceuticals Compositions and Uses Thereof
, pp. 1-52
-
-
Gallop, M.A.1
-
69
-
-
0034868135
-
Targeting the sodium-dependent multivitamin transporter (SMVT) for improving the oral absorption properties of a retro-inverso Tat nonapeptide
-
Ramanathan S., et al. Targeting the sodium-dependent multivitamin transporter (SMVT) for improving the oral absorption properties of a retro-inverso Tat nonapeptide. Pharm. Res. 2001, 18(7):950-956.
-
(2001)
Pharm. Res.
, vol.18
, Issue.7
, pp. 950-956
-
-
Ramanathan, S.1
-
70
-
-
0036354863
-
Enhancing the anticancer efficacy of camptothecin using biotinylated poly(ethylene glycol) conjugates in sensitive and multidrug-resistant human ovarian carcinoma cells
-
Minko T., et al. Enhancing the anticancer efficacy of camptothecin using biotinylated poly(ethylene glycol) conjugates in sensitive and multidrug-resistant human ovarian carcinoma cells. Cancer Chemother. Pharmacol. 2002, 50(2):143-150.
-
(2002)
Cancer Chemother. Pharmacol.
, vol.50
, Issue.2
, pp. 143-150
-
-
Minko, T.1
-
71
-
-
5344270492
-
Vitamin-mediated targeting as a potential mechanism to increase drug uptake by tumours
-
Russell-Jones G., et al. Vitamin-mediated targeting as a potential mechanism to increase drug uptake by tumours. J. Inorg. Biochem. 2004, 98(10):1625-1633.
-
(2004)
J. Inorg. Biochem.
, vol.98
, Issue.10
, pp. 1625-1633
-
-
Russell-Jones, G.1
-
72
-
-
60149100143
-
Targeting cancer cells with biotin-dendrimer conjugates
-
Yang W., et al. Targeting cancer cells with biotin-dendrimer conjugates. Eur. J. Med. Chem. 2009, 44(2):862-868.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, Issue.2
, pp. 862-868
-
-
Yang, W.1
-
73
-
-
0028337034
-
Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice
-
Yamaoka T., Tabata Y., Ikada Y. Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice. J. Pharm. Sci. 1994, 83(4):601-606.
-
(1994)
J. Pharm. Sci.
, vol.83
, Issue.4
, pp. 601-606
-
-
Yamaoka, T.1
Tabata, Y.2
Ikada, Y.3
-
74
-
-
84877857970
-
NKTR-102, a novel PEGylated-irinotecan conjugate, results in sustained tumor growth inhibition in mouse models of human colorectal and lung tumors that is associated with increased and sustained tumor SN38 exposure
-
Eldon Michael A., C.-M.S., Viegas Tacey, Bentley Michael NKTR-102, a novel PEGylated-irinotecan conjugate, results in sustained tumor growth inhibition in mouse models of human colorectal and lung tumors that is associated with increased and sustained tumor SN38 exposure. The 2007 AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics 2007, C157.
-
(2007)
The 2007 AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics
-
-
Eldon, M.A.C.-M.S.1
Viegas, T.2
Bentley, M.3
-
75
-
-
55749093123
-
Anti-tumor activity and pharmacokinetics of NKTR-102, a novel PEGylated-irinotecan conjugate, in irinotecan-resistant colorectal tumors implanted in mice
-
Eldon Michael A., L.A., Staschen Carl-Michael, Viegas Tacey, Singhal Anil, M.R., Persson Heather, Bentley Michael Anti-tumor activity and pharmacokinetics of NKTR-102, a novel PEGylated-irinotecan conjugate, in irinotecan-resistant colorectal tumors implanted in mice. 14th European Cancer Conference 2007, P-0722.
-
(2007)
14th European Cancer Conference
-
-
Eldon, M.A.L.A.1
Staschen, C.-M.2
Viegas, T.3
Singhal, A.M.R.4
Persson, H.5
Bentley, M.6
-
76
-
-
79960006474
-
-
Von Hoff D.D., G.S.J., Borad M.J., Rosen L.S., Utz4 J., Basche M., Alemany C., Dhar S., Acosta L., Barker T., Walling J., Hamm J.T. First Phase I Trial of NKTR-102 (PEG-irinotecan) Reveals Early Evidence of Broad Anti-Tumor Activity in Three Different Schedules in 2008 EORTC-NCI-AACR Symposium 2008, P-595.
-
(2008)
First Phase I Trial of NKTR-102 (PEG-irinotecan) Reveals Early Evidence of Broad Anti-Tumor Activity in Three Different Schedules in 2008 EORTC-NCI-AACR Symposium
-
-
Von Hoff, D.D.G.S.J.1
Borad, M.J.2
Rosen, L.S.3
Utz4, J.4
Basche, M.5
Alemany, C.6
Dhar, S.7
Acosta, L.8
Barker, T.9
Walling, J.10
Hamm, J.T.11
-
77
-
-
79959941999
-
Polymer therapeutics: polymers as drugs, conjugates and gene delivery systems
-
Ronit Satchi-Fainaro R.D. Polymer therapeutics: polymers as drugs, conjugates and gene delivery systems. Advances in polymer science 2006, 36-37.
-
(2006)
Advances in polymer science
, pp. 36-37
-
-
Ronit Satchi-Fainaro, R.D.1
-
78
-
-
41549105038
-
Novel delivery of SN38 markedly inhibits tumor growth in xenografts, including a camptothecin-11-refractory model
-
Sapra P., et al. Novel delivery of SN38 markedly inhibits tumor growth in xenografts, including a camptothecin-11-refractory model. Clin. Cancer Res. 2008, 14(6):1888-1896.
-
(2008)
Clin. Cancer Res.
, vol.14
, Issue.6
, pp. 1888-1896
-
-
Sapra, P.1
-
79
-
-
79960005905
-
NKTR-118 (oral PEG-Naloxol), a PEGylated derivative of Naloxone: demonstration of selective peripheral opioid antagonism after oral administration in preclinical models
-
Eldon Michael A., Neumann Theresa A., Wolff Ron, Cheng Lin, Viegas †Tacey X., Bentley †Michael D., Fishburn C.Simone, Kugler Alan R. NKTR-118 (oral PEG-Naloxol), a PEGylated derivative of Naloxone: demonstration of selective peripheral opioid antagonism after oral administration in preclinical models. The American Academy of Pain Management 18th Annual Clinical Meeting 2007, P-28.
-
(2007)
The American Academy of Pain Management 18th Annual Clinical Meeting
-
-
Eldon, M.A.1
Neumann, T.A.2
Wolff, R.3
Cheng, L.4
Viegas, †.X.5
Bentley, †.D.6
Fishburn, C.S.7
Kugler, A.R.8
-
80
-
-
79960000196
-
Clinical investigation of NKTR-118 as a Selective oral peripheral opioid antagonist
-
Neumann Theresa A., Marcantonio Annette, Song Di, Morrison Paul J., Eldon Michael A., Kugler Alan R. Clinical investigation of NKTR-118 as a Selective oral peripheral opioid antagonist. The American Academy of Pain Management 18th Annual Clinical Meeting 2007, P-27.
-
(2007)
The American Academy of Pain Management 18th Annual Clinical Meeting
-
-
Neumann, T.A.1
Marcantonio, A.2
Song, D.3
Morrison, P.J.4
Eldon, M.A.5
Kugler, A.R.6
-
81
-
-
12744278961
-
Phase II study of CT-2103 in patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal carcinoma
-
Sabbatini P., et al. Phase II study of CT-2103 in patients with recurrent epithelial ovarian, fallopian tube, or primary peritoneal carcinoma. J. Clin. Oncol. 2004, 22(22):4523-4531.
-
(2004)
J. Clin. Oncol.
, vol.22
, Issue.22
, pp. 4523-4531
-
-
Sabbatini, P.1
-
82
-
-
0032959549
-
Phase I clinical and pharmacokinetic study of PK1 [N-(2-hydroxypropyl)methacrylamide copolymer doxorubicin]: first member of a new class of chemotherapeutic agents-drug-polymer conjugates. Cancer Research Campaign Phase I/II Committee
-
Vasey P.A., et al. Phase I clinical and pharmacokinetic study of PK1 [N-(2-hydroxypropyl)methacrylamide copolymer doxorubicin]: first member of a new class of chemotherapeutic agents-drug-polymer conjugates. Cancer Research Campaign Phase I/II Committee. Clin. Cancer Res. 1999, 5(1):83-94.
-
(1999)
Clin. Cancer Res.
, vol.5
, Issue.1
, pp. 83-94
-
-
Vasey, P.A.1
-
83
-
-
67649417879
-
Phase II studies of polymer-doxorubicin (PK1, FCE28068) in the treatment of breast, lung and colorectal cancer
-
Seymour L.W., et al. Phase II studies of polymer-doxorubicin (PK1, FCE28068) in the treatment of breast, lung and colorectal cancer. Int. J. Oncol. 2009, 34(6):1629-1636.
-
(2009)
Int. J. Oncol.
, vol.34
, Issue.6
, pp. 1629-1636
-
-
Seymour, L.W.1
-
84
-
-
0037413560
-
Synthesis and in vivo antitumor activity of poly(l-glutamic acid) conjugates of 20S-camptothecin
-
Bhatt R., et al. Synthesis and in vivo antitumor activity of poly(l-glutamic acid) conjugates of 20S-camptothecin. J. Med. Chem. 2003, 46(1):190-193.
-
(2003)
J. Med. Chem.
, vol.46
, Issue.1
, pp. 190-193
-
-
Bhatt, R.1
-
85
-
-
34250612643
-
Phase II study of CT-2103 as first- or second-line chemotherapy in patients with metastatic breast cancer: unexpected incidence of hypersensitivity reactions
-
Lin N.U., et al. Phase II study of CT-2103 as first- or second-line chemotherapy in patients with metastatic breast cancer: unexpected incidence of hypersensitivity reactions. Invest. New Drugs 2007, 25(4):369-375.
-
(2007)
Invest. New Drugs
, vol.25
, Issue.4
, pp. 369-375
-
-
Lin, N.U.1
-
86
-
-
35348868039
-
Phase I trial of poly-l-glutamate camptothecin (CT-2106) administered weekly in patients with advanced solid malignancies
-
Homsi J., et al. Phase I trial of poly-l-glutamate camptothecin (CT-2106) administered weekly in patients with advanced solid malignancies. Clin. Cancer Res. 2007, 13(19):5855-5861.
-
(2007)
Clin. Cancer Res.
, vol.13
, Issue.19
, pp. 5855-5861
-
-
Homsi, J.1
-
87
-
-
42649145864
-
Poly (amino acid) micelle nanocarriers in preclinical and clinical studies
-
Matsumura Y. Poly (amino acid) micelle nanocarriers in preclinical and clinical studies. Adv. Drug Deliv. Rev. 2008, 60(8):899-914.
-
(2008)
Adv. Drug Deliv. Rev.
, vol.60
, Issue.8
, pp. 899-914
-
-
Matsumura, Y.1
-
88
-
-
58849083140
-
A dose-finding pharmacokinetic study of IT-101, the first de novo designed nanoparticle therapeutic, in refractory solid tumors
-
Oliver J.C., Y.Y., Synold T.W., Schluep T., Davis M. A dose-finding pharmacokinetic study of IT-101, the first de novo designed nanoparticle therapeutic, in refractory solid tumors. 2008 ASCO Annual Meeting Proceedings 2008.
-
(2008)
2008 ASCO Annual Meeting Proceedings
-
-
Oliver, J.C.Y.Y.1
Synold, T.W.2
Schluep, T.3
Davis, M.4
-
89
-
-
17644366858
-
A folate receptor-targeted lipid nanoparticle formulation for a lipophilic paclitaxel prodrug
-
Stevens P.J., Sekido M., Lee R.J. A folate receptor-targeted lipid nanoparticle formulation for a lipophilic paclitaxel prodrug. Pharm. Res. 2004, 21(12):2153-2157.
-
(2004)
Pharm. Res.
, vol.21
, Issue.12
, pp. 2153-2157
-
-
Stevens, P.J.1
Sekido, M.2
Lee, R.J.3
-
90
-
-
0024562089
-
Semenogelin, the predominant protein in human semen. Primary structure and identification of closely related proteins in the male accessory sex glands and on the spermatozoa
-
Lilja H., Abrahamsson P.A., Lundwall A. Semenogelin, the predominant protein in human semen. Primary structure and identification of closely related proteins in the male accessory sex glands and on the spermatozoa. J. Biol. Chem. 1989, 264(3):1894-1900.
-
(1989)
J. Biol. Chem.
, vol.264
, Issue.3
, pp. 1894-1900
-
-
Lilja, H.1
Abrahamsson, P.A.2
Lundwall, A.3
-
91
-
-
41249085384
-
Targeted inhibition of hedgehog signaling by cyclopamine prodrugs for advanced prostate cancer
-
Kumar S.K., et al. Targeted inhibition of hedgehog signaling by cyclopamine prodrugs for advanced prostate cancer. Bioorg. Med. Chem. 2008, 16(6):2764-2768.
-
(2008)
Bioorg. Med. Chem.
, vol.16
, Issue.6
, pp. 2764-2768
-
-
Kumar, S.K.1
-
92
-
-
0037009238
-
A 5-fluorodeoxyuridine prodrug as targeted therapy for prostate cancer
-
Mhaka A., et al. A 5-fluorodeoxyuridine prodrug as targeted therapy for prostate cancer. Bioorg. Med. Chem. Lett. 2002, 12(17):2459-2461.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, Issue.17
, pp. 2459-2461
-
-
Mhaka, A.1
-
93
-
-
34249690674
-
Modulating paclitaxel bioavailability for targeting prostate cancer
-
Kumar S.K., et al. Modulating paclitaxel bioavailability for targeting prostate cancer. Bioorg. Med. Chem. 2007, 15(14):4973-4984.
-
(2007)
Bioorg. Med. Chem.
, vol.15
, Issue.14
, pp. 4973-4984
-
-
Kumar, S.K.1
-
94
-
-
0032526152
-
Enzymatic activation of a doxorubicin-peptide prodrug by prostate-specific antigen
-
Denmeade S.R., et al. Enzymatic activation of a doxorubicin-peptide prodrug by prostate-specific antigen. Cancer Res. 1998, 58(12):2537-2540.
-
(1998)
Cancer Res.
, vol.58
, Issue.12
, pp. 2537-2540
-
-
Denmeade, S.R.1
-
95
-
-
0042308774
-
Prostate-specific antigen-activated thapsigargin prodrug as targeted therapy for prostate cancer
-
Denmeade S.R., et al. Prostate-specific antigen-activated thapsigargin prodrug as targeted therapy for prostate cancer. J. Natl Cancer Inst. 2003, 95(13):990-1000.
-
(2003)
J. Natl Cancer Inst.
, vol.95
, Issue.13
, pp. 990-1000
-
-
Denmeade, S.R.1
-
96
-
-
0035935668
-
The synthesis of a prodrug of doxorubicin designed to provide reduced systemic toxicity and greater target efficacy
-
Garsky V.M., et al. The synthesis of a prodrug of doxorubicin designed to provide reduced systemic toxicity and greater target efficacy. J. Med. Chem. 2001, 44(24):4216-4224.
-
(2001)
J. Med. Chem.
, vol.44
, Issue.24
, pp. 4216-4224
-
-
Garsky, V.M.1
-
97
-
-
3843113671
-
Tumor target prostate specific membrane antigen (PSMA) and its regulation in prostate cancer
-
Ghosh A., Heston W.D. Tumor target prostate specific membrane antigen (PSMA) and its regulation in prostate cancer. J. Cell. Biochem. 2004, 91(3):528-539.
-
(2004)
J. Cell. Biochem.
, vol.91
, Issue.3
, pp. 528-539
-
-
Ghosh, A.1
Heston, W.D.2
-
98
-
-
0346333234
-
Correlation of primary tumor prostate-specific membrane antigen expression with disease recurrence in prostate cancer
-
Ross J.S., et al. Correlation of primary tumor prostate-specific membrane antigen expression with disease recurrence in prostate cancer. Clin. Cancer Res. 2003, 9(17):6357-6362.
-
(2003)
Clin. Cancer Res.
, vol.9
, Issue.17
, pp. 6357-6362
-
-
Ross, J.S.1
-
99
-
-
0030219893
-
Upregulation of prostate-specific membrane antigen after androgen-deprivation therapy
-
Wright G.L., et al. Upregulation of prostate-specific membrane antigen after androgen-deprivation therapy. Urology 1996, 48(2):326-334.
-
(1996)
Urology
, vol.48
, Issue.2
, pp. 326-334
-
-
Wright, G.L.1
-
100
-
-
21644470680
-
Use of methotrexate-based peptide substrates to characterize the substrate specificity of prostate-specific membrane antigen (PSMA)
-
Mhaka A., et al. Use of methotrexate-based peptide substrates to characterize the substrate specificity of prostate-specific membrane antigen (PSMA). Cancer Biol. Ther. 2004, 3(6):551-558.
-
(2004)
Cancer Biol. Ther.
, vol.3
, Issue.6
, pp. 551-558
-
-
Mhaka, A.1
-
101
-
-
0027355456
-
Antibody-directed enzyme prodrug therapy (ADEPT)
-
Bagshawe K.D. Antibody-directed enzyme prodrug therapy (ADEPT). Adv. Pharmacol. 1993, 24:99-121.
-
(1993)
Adv. Pharmacol.
, vol.24
, pp. 99-121
-
-
Bagshawe, K.D.1
-
102
-
-
0029102762
-
Prodrugs in cancer chemotherapy
-
Connor T.A. Prodrugs in cancer chemotherapy. Stem Cells 1995, 13(5):501-511.
-
(1995)
Stem Cells
, vol.13
, Issue.5
, pp. 501-511
-
-
Connor, T.A.1
-
103
-
-
0030024847
-
Antibody-enzyme conjugates for cancer therapy
-
Melton R.G., Sherwood R.F. Antibody-enzyme conjugates for cancer therapy. J. Natl Cancer Inst. 1996, 88(3-4):153-165.
-
(1996)
J. Natl Cancer Inst.
, vol.88
, Issue.3-4
, pp. 153-165
-
-
Melton, R.G.1
Sherwood, R.F.2
-
104
-
-
0030002918
-
Antibody-directed enzyme prodrug therapy (ADEPT)
-
Melton R.G. Antibody-directed enzyme prodrug therapy (ADEPT). Drugs Future 1996, 21:167.
-
(1996)
Drugs Future
, vol.21
, pp. 167
-
-
Melton, R.G.1
-
106
-
-
0036715292
-
A Phase I study of combined modality (90)Yttrium-CC49 intraperitoneal radioimmunotherapy for ovarian cancer
-
Alvarez R.D., et al. A Phase I study of combined modality (90)Yttrium-CC49 intraperitoneal radioimmunotherapy for ovarian cancer. Clin. Cancer Res. 2002, 8(9):2806-2811.
-
(2002)
Clin. Cancer Res.
, vol.8
, Issue.9
, pp. 2806-2811
-
-
Alvarez, R.D.1
-
107
-
-
20144389618
-
Pharmacokinetics and clinical evaluation of 125I-radiolabeled humanized CC49 monoclonal antibody (HuCC49deltaC(H)2) in recurrent and metastatic colorectal cancer patients
-
Xiao J., et al. Pharmacokinetics and clinical evaluation of 125I-radiolabeled humanized CC49 monoclonal antibody (HuCC49deltaC(H)2) in recurrent and metastatic colorectal cancer patients. Cancer Biother. Radiopharm. 2005, 20(1):16-26.
-
(2005)
Cancer Biother. Radiopharm.
, vol.20
, Issue.1
, pp. 16-26
-
-
Xiao, J.1
-
108
-
-
33750107199
-
Enzyme specific activation of benzoquinone ansamycin prodrugs using HuCC49DeltaCH2-beta-galactosidase conjugates
-
Fang L., et al. Enzyme specific activation of benzoquinone ansamycin prodrugs using HuCC49DeltaCH2-beta-galactosidase conjugates. J. Med. Chem. 2006, 49(21):6290-6297.
-
(2006)
J. Med. Chem.
, vol.49
, Issue.21
, pp. 6290-6297
-
-
Fang, L.1
-
109
-
-
18544390790
-
A phase I trial of antibody directed enzyme prodrug therapy (ADEPT) in patients with advanced colorectal carcinoma or other CEA producing tumours
-
Francis R.J., et al. A phase I trial of antibody directed enzyme prodrug therapy (ADEPT) in patients with advanced colorectal carcinoma or other CEA producing tumours. Br. J. Cancer 2002, 87(6):600-607.
-
(2002)
Br. J. Cancer
, vol.87
, Issue.6
, pp. 600-607
-
-
Francis, R.J.1
-
110
-
-
0032806082
-
Genetic prodrug activation therapy for pancreatic cancer
-
Rigg A.S., Lemoine N.R. Genetic prodrug activation therapy for pancreatic cancer. Ann. NY Acad. Sci. 1999, 880:319-325.
-
(1999)
Ann. NY Acad. Sci.
, vol.880
, pp. 319-325
-
-
Rigg, A.S.1
Lemoine, N.R.2
-
111
-
-
0027483695
-
The "bystander effect": tumor regression when a fraction of the tumor mass is genetically modified
-
Freeman S.M., et al. The "bystander effect": tumor regression when a fraction of the tumor mass is genetically modified. Cancer Res. 1993, 53(21):5274-5283.
-
(1993)
Cancer Res.
, vol.53
, Issue.21
, pp. 5274-5283
-
-
Freeman, S.M.1
-
112
-
-
0027787053
-
In vitro evidence that metabolic cooperation is responsible for the bystander effect observed with HSV tk retroviral gene therapy
-
Bi W.L., et al. In vitro evidence that metabolic cooperation is responsible for the bystander effect observed with HSV tk retroviral gene therapy. Hum. Gene Ther. 1993, 4(6):725-731.
-
(1993)
Hum. Gene Ther.
, vol.4
, Issue.6
, pp. 725-731
-
-
Bi, W.L.1
-
113
-
-
0028108469
-
Metabolism of 5-fluorocytosine to 5-fluorouracil in human colorectal tumor cells transduced with the cytosine deaminase gene: significant antitumor effects when only a small percentage of tumor cells express cytosine deaminase
-
Huber B.E., et al. Metabolism of 5-fluorocytosine to 5-fluorouracil in human colorectal tumor cells transduced with the cytosine deaminase gene: significant antitumor effects when only a small percentage of tumor cells express cytosine deaminase. Proc. Natl Acad. Sci. USA 1994, 91(17):8302-8306.
-
(1994)
Proc. Natl Acad. Sci. USA
, vol.91
, Issue.17
, pp. 8302-8306
-
-
Huber, B.E.1
-
114
-
-
0033022611
-
Genetic prodrug activation therapy for breast cancer: a phase I clinical trial of erbB-2-directed suicide gene expression
-
Pandha H.S., et al. Genetic prodrug activation therapy for breast cancer: a phase I clinical trial of erbB-2-directed suicide gene expression. J. Clin. Oncol. 1999, 17(7):2180-2189.
-
(1999)
J. Clin. Oncol.
, vol.17
, Issue.7
, pp. 2180-2189
-
-
Pandha, H.S.1
-
115
-
-
0030459592
-
Suicide gene expression induced in tumour cells transduced with recombinant adenoviral, retroviral and plasmid vectors containing the ERBB2 promoter
-
Ring C.J., et al. Suicide gene expression induced in tumour cells transduced with recombinant adenoviral, retroviral and plasmid vectors containing the ERBB2 promoter. Gene Ther. 1996, 3(12):1094-1103.
-
(1996)
Gene Ther.
, vol.3
, Issue.12
, pp. 1094-1103
-
-
Ring, C.J.1
-
116
-
-
0030730794
-
Use of transcriptional regulatory elements of the MUC1 and ERBB2 genes to drive tumour-selective expression of a prodrug activating enzyme
-
Ring C.J., et al. Use of transcriptional regulatory elements of the MUC1 and ERBB2 genes to drive tumour-selective expression of a prodrug activating enzyme. Gene Ther. 1997, 4(10):1045-1052.
-
(1997)
Gene Ther.
, vol.4
, Issue.10
, pp. 1045-1052
-
-
Ring, C.J.1
-
117
-
-
0347003567
-
Multiple modifications allow high-titer production of retroviral vectors carrying heterologous regulatory elements
-
Hlavaty J., et al. Multiple modifications allow high-titer production of retroviral vectors carrying heterologous regulatory elements. J. Virol. 2004, 78(3):1384-1392.
-
(2004)
J. Virol.
, vol.78
, Issue.3
, pp. 1384-1392
-
-
Hlavaty, J.1
-
118
-
-
52149089437
-
Prodrug cancer gene therapy
-
Altaner C. Prodrug cancer gene therapy. Cancer Lett. 2008, 270(2):191-201.
-
(2008)
Cancer Lett.
, vol.270
, Issue.2
, pp. 191-201
-
-
Altaner, C.1
-
119
-
-
0034834392
-
Chimeric PSA enhancers exhibit augmented activity in prostate cancer gene therapy vectors
-
Wu L., et al. Chimeric PSA enhancers exhibit augmented activity in prostate cancer gene therapy vectors. Gene Ther. 2001, 8(18):1416-1426.
-
(2001)
Gene Ther.
, vol.8
, Issue.18
, pp. 1416-1426
-
-
Wu, L.1
-
120
-
-
23944447580
-
Enantioselective metabolism and cytotoxicity of R-ifosfamide and S-ifosfamide by tumor cell-expressed cytochromes P450
-
Chen C.S., Jounaidi Y., Waxman D.J. Enantioselective metabolism and cytotoxicity of R-ifosfamide and S-ifosfamide by tumor cell-expressed cytochromes P450. Drug Metab. Dispos. 2005, 33(9):1261-1267.
-
(2005)
Drug Metab. Dispos.
, vol.33
, Issue.9
, pp. 1261-1267
-
-
Chen, C.S.1
Jounaidi, Y.2
Waxman, D.J.3
-
121
-
-
0037279816
-
Bioreductive GDEPT using cytochrome P450 3A4 in combination with AQ4N
-
McCarthy H.O., et al. Bioreductive GDEPT using cytochrome P450 3A4 in combination with AQ4N. Cancer Gene Ther. 2003, 10(1):40-48.
-
(2003)
Cancer Gene Ther.
, vol.10
, Issue.1
, pp. 40-48
-
-
McCarthy, H.O.1
-
122
-
-
65049088393
-
Potentiation of methoxymorpholinyl doxorubicin antitumor activity by P450 3A4 gene transfer
-
Lu H., Chen C.S., Waxman D.J. Potentiation of methoxymorpholinyl doxorubicin antitumor activity by P450 3A4 gene transfer. Cancer Gene Ther. 2009, 16(5):393-404.
-
(2009)
Cancer Gene Ther.
, vol.16
, Issue.5
, pp. 393-404
-
-
Lu, H.1
Chen, C.S.2
Waxman, D.J.3
-
123
-
-
33847212832
-
Five-year follow-up of trial of replication-competent adenovirus-mediated suicide gene therapy for treatment of prostate cancer
-
Freytag S.O., et al. Five-year follow-up of trial of replication-competent adenovirus-mediated suicide gene therapy for treatment of prostate cancer. Mol. Ther. 2007, 15(3):636-642.
-
(2007)
Mol. Ther.
, vol.15
, Issue.3
, pp. 636-642
-
-
Freytag, S.O.1
-
124
-
-
10744227813
-
Phase I study of replication-competent adenovirus-mediated double-suicide gene therapy in combination with conventional-dose three-dimensional conformal radiation therapy for the treatment of newly diagnosed, intermediate- to high-risk prostate cancer
-
Freytag S.O., et al. Phase I study of replication-competent adenovirus-mediated double-suicide gene therapy in combination with conventional-dose three-dimensional conformal radiation therapy for the treatment of newly diagnosed, intermediate- to high-risk prostate cancer. Cancer Res. 2003, 63(21):7497-7506.
-
(2003)
Cancer Res.
, vol.63
, Issue.21
, pp. 7497-7506
-
-
Freytag, S.O.1
-
125
-
-
2442767029
-
A phase I/II study of herpes simplex virus type 1 thymidine kinase "suicide" gene therapy for recurrent glioblastoma. Study Group on Gene Therapy for Glioblastoma
-
Klatzmann D., et al. A phase I/II study of herpes simplex virus type 1 thymidine kinase "suicide" gene therapy for recurrent glioblastoma. Study Group on Gene Therapy for Glioblastoma. Hum. Gene Ther. 1998, 9(17):2595-2604.
-
(1998)
Hum. Gene Ther.
, vol.9
, Issue.17
, pp. 2595-2604
-
-
Klatzmann, D.1
-
126
-
-
0037832252
-
Suicide gene therapy mediated by the Herpes Simplex virus thymidine kinase gene/Ganciclovir system: fifteen years of application
-
Fillat C., et al. Suicide gene therapy mediated by the Herpes Simplex virus thymidine kinase gene/Ganciclovir system: fifteen years of application. Curr. Gene Ther. 2003, 3(1):13-26.
-
(2003)
Curr. Gene Ther.
, vol.3
, Issue.1
, pp. 13-26
-
-
Fillat, C.1
-
127
-
-
31644447744
-
Response of retinoblastoma with vitreous tumor seeding to adenovirus-mediated delivery of thymidine kinase followed by ganciclovir
-
Chevez-Barrios P., et al. Response of retinoblastoma with vitreous tumor seeding to adenovirus-mediated delivery of thymidine kinase followed by ganciclovir. J. Clin. Oncol. 2005, 23(31):7927-7935.
-
(2005)
J. Clin. Oncol.
, vol.23
, Issue.31
, pp. 7927-7935
-
-
Chevez-Barrios, P.1
-
128
-
-
0036909628
-
Cytochrome P450-based cancer gene therapy: current status
-
Kan O., Kingsman S., Naylor S. Cytochrome P450-based cancer gene therapy: current status. Expert Opin. Biol. Ther. 2002, 2(8):857-868.
-
(2002)
Expert Opin. Biol. Ther.
, vol.2
, Issue.8
, pp. 857-868
-
-
Kan, O.1
Kingsman, S.2
Naylor, S.3
-
129
-
-
20044363101
-
Phase I study of MetXia-P450 gene therapy and oral cyclophosphamide for patients with advanced breast cancer or melanoma
-
Braybrooke J.P., et al. Phase I study of MetXia-P450 gene therapy and oral cyclophosphamide for patients with advanced breast cancer or melanoma. Clin. Cancer Res. 2005, 11(4):1512-1520.
-
(2005)
Clin. Cancer Res.
, vol.11
, Issue.4
, pp. 1512-1520
-
-
Braybrooke, J.P.1
-
130
-
-
9344252858
-
Nitroreductase: a prodrug-activating enzyme for cancer gene therapy
-
Searle P.F., et al. Nitroreductase: a prodrug-activating enzyme for cancer gene therapy. Clin. Exp. Pharmacol. Physiol. 2004, 31(11):811-816.
-
(2004)
Clin. Exp. Pharmacol. Physiol.
, vol.31
, Issue.11
, pp. 811-816
-
-
Searle, P.F.1
-
131
-
-
2442696806
-
Virus-directed enzyme prodrug therapy: intratumoral administration of a replication-deficient adenovirus encoding nitroreductase to patients with resectable liver cancer
-
Palmer D.H., et al. Virus-directed enzyme prodrug therapy: intratumoral administration of a replication-deficient adenovirus encoding nitroreductase to patients with resectable liver cancer. J. Clin. Oncol. 2004, 22(9):1546-1552.
-
(2004)
J. Clin. Oncol.
, vol.22
, Issue.9
, pp. 1546-1552
-
-
Palmer, D.H.1
-
132
-
-
0034814342
-
Virus-directed, enzyme prodrug therapy with nitroimidazole reductase: a phase I and pharmacokinetic study of its prodrug, CB1954
-
Chung-Faye G., et al. Virus-directed, enzyme prodrug therapy with nitroimidazole reductase: a phase I and pharmacokinetic study of its prodrug, CB1954. Clin. Cancer Res. 2001, 7(9):2662-2668.
-
(2001)
Clin. Cancer Res.
, vol.7
, Issue.9
, pp. 2662-2668
-
-
Chung-Faye, G.1
-
133
-
-
0030971014
-
Antibody-directed enzyme prodrug therapy: pharmacokinetics and plasma levels of prodrug and drug in a phase I clinical trial
-
Martin J., et al. Antibody-directed enzyme prodrug therapy: pharmacokinetics and plasma levels of prodrug and drug in a phase I clinical trial. Cancer Chemother. Pharmacol. 1997, 40(3):189-201.
-
(1997)
Cancer Chemother. Pharmacol.
, vol.40
, Issue.3
, pp. 189-201
-
-
Martin, J.1
-
134
-
-
12944288238
-
Antibody-directed enzyme prodrug therapy: efficacy and mechanism of action in colorectal carcinoma
-
Napier M.P., et al. Antibody-directed enzyme prodrug therapy: efficacy and mechanism of action in colorectal carcinoma. Clin. Cancer Res. 2000, 6(3):765-772.
-
(2000)
Clin. Cancer Res.
, vol.6
, Issue.3
, pp. 765-772
-
-
Napier, M.P.1
|