Drug-targeting strategies in cancer therapy

被引:63
作者
Huang, PS [1 ]
Oliff, A [1 ]
机构
[1] Dupont Pharmaceut Co, Dept Canc Res, Glenolden, PA 19036 USA
关键词
D O I
10.1016/S0959-437X(00)00164-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genetic changes in cell-cycle, apoptotic, and survival pathways cause tumorigenesis, leading to significant phenotypic changes in transformed cells. These changes in the tumor environment - elevated expression of surface proteases, increased angiogenesis and glucuronidase activity - can be taken advantage of to improve the therapeutic index of exisiting cancer therapies. Targeting cytotoxics to tumor cells by enzymatic activation is a promising strategy for improving chemotherapeutics.
引用
收藏
页码:104 / 110
页数:7
相关论文
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[1]  
Ahmad I, 1999, ONCOL RES, V11, P273
[2]   Doxorubicin represses CARP gene transcription through the generation of oxidative stress in neonatal rat cardiac myocytes: Possible role of serine/threonine kinase-dependent pathways [J].
Aihara, Y ;
Kurabayashi, M ;
Tanaka, T ;
Takeda, S ;
Tomaru, K ;
Sekiguchi, K ;
Ohyama, Y ;
Nagai, R .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (08) :1401-1414
[3]   Intensely cytotoxic anthracycline prodrugs: Glucuronides [J].
Bakina, E ;
Wu, Z ;
Rosenblum, M ;
Farquhar, D .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (25) :4013-4018
[4]   Inhibition of growth and metastatic progression of pancreatic carcinoma in hamster after somatostatin receptor subtype 2 (sst2) gene expression and administration of cytotoxic somatostatin analog AN-238 [J].
Benali, N ;
Cordelier, P ;
Calise, D ;
Pagès, P ;
Rochaix, P ;
Nagy, A ;
Estève, JP ;
Pour, PM ;
Schally, AV ;
Vaysse, N ;
Susini, C ;
Buscail, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :9180-9185
[5]  
Bosslet K, 1998, CANCER RES, V58, P1195
[6]   The antitumour activity of the prodrug N-L-leucyl-doxorubicin and its parent compound doxorubicin in human tumour xenografts [J].
Breistol, K ;
Hendriks, HR ;
Berger, DP ;
Langdon, SP ;
Fiebig, HH ;
Fodstad, O .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (10) :1602-1606
[7]   Superior therapeutic efficacy of N-L-leucyl-doxorubicin versus doxorubicin in human melanoma xenografts correlates with higher tumour concentrations of free drug [J].
Breistol, K ;
Hendriks, HR ;
Fodstad, O .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (07) :1143-1149
[8]   Synthesis and biological evaluation of 2′-carbamate-linked and 2′-carbonate-linked prodrugs of paclitaxel:: Selective activation by the tumor-associated protease plasmin [J].
de Groot, FMH ;
van Berkom, LWA ;
Scheeren, HW .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (16) :3093-3102
[9]   Synthesis and biological evaluation of novel prodrugs of anthracyclines for selective activation by the tumor-associated protease plasmin [J].
de Groot, FMH ;
de Bart, ACW ;
Verheijen, JH ;
Scheeren, HW .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (25) :5277-5283
[10]   A peptide-doxorubicin 'prodrug' activated by prostate-specific antigen selectively kills prostate tumor cells positive for prostate-specific antigen in vivo [J].
DeFeo-Jones, D ;
Garsky, VM ;
Wong, BK ;
Feng, DM ;
Bolyar, T ;
Haskell, K ;
Kiefer, DM ;
Leander, K ;
McAvoy, E ;
Lumma, P ;
Wai, J ;
Senderak, ET ;
Motzel, SL ;
Keenan, K ;
Van Zwieten, M ;
Lin, JH ;
Freidinger, R ;
Huff, J ;
Oliff, A ;
Jones, RE .
NATURE MEDICINE, 2000, 6 (11) :1248-1252