The chloroethylnitrosoureas sensitivity and resistance to cancer chemotherapy at the molecular level

被引:64
作者
Ludlum, DB
机构
[1] Dept. Pharmacol. and Molec. Toxicol., Univ. of Massachusetts Med. School, Worcester
关键词
D O I
10.3109/07357909709047601
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The chloroethylnitrosoureas were developed in a synthetic program that began with the observation that N-methyl-N'-nitro-N-nitrosoguanidine was an effective agent against L1210 cells. The antitumor activity of the chloroethylnitrosoureas is based on their reactions with DNA, especially the formation of a cytosine-guanine crosslink in DNA. Resistance occurs when the enzyme, O-6-alkylguanine-DNA alkyltransferase, repairs an intermediate in crosslink formation. Inhibition of O-6-alkylguanine-DNA alkyltransferase often restores sensitivity to the chloroethylnitrosoureas although evidence is accumulating that other repair mechanisms may also contribute to the resistance phenomenon. Continuing investigations in this field center on finding agents whose reactions with DNA are more specific, on elucidating other resistance mechanisms, and on overcoming resistance by developing new inhibitors of repair enzymes.
引用
收藏
页码:588 / 598
页数:11
相关论文
共 68 条
[1]  
ALIOSMAN F, 1989, CANCER RES, V49, P5258
[2]   RETROVIRAL TRANSDUCTION AND EXPRESSION OF THE HUMAN ALKYLTRANSFERASE CDNA PROVIDES NITROSOUREA RESISTANCE TO HEMATOPOIETIC-CELLS [J].
ALLAY, JA ;
DUMENCO, LL ;
KOC, ON ;
LIU, L ;
GERSON, SL .
BLOOD, 1995, 85 (11) :3342-3351
[3]  
Belanich M, 1996, CANCER RES, V56, P783
[4]  
BENNETT RA, 1981, CANCER RES, V41, P2786
[5]  
BODELL WJ, 1988, CANCER RES, V48, P4489
[6]   CHEMICAL SYNTHESIS AND DETECTION OF THE CROSS-LINK 1-[N3-(2'-DEOXYCYTIDYL)]-2-[N1-(2'-DEOXYGUANOSINYL)]ETHANE IN DNA REACTED WITH 1-(2-CHLOROETHYL)-1-NITROSOUREA [J].
BODELL, WJ ;
PONGRACZ, K .
CHEMICAL RESEARCH IN TOXICOLOGY, 1993, 6 (04) :434-438
[7]  
BRENT TP, 1984, CANCER RES, V44, P1887
[8]   REPAIR OF 1-(2-CHLOROETHYL)-3-CYCLOHEXYL-1-NITROSOUREA-INDUCED DAMAGE BY MAMMALIAN-CELL EXTRACTS [J].
CAPPELLI, E ;
REDAELLI, A ;
RIVANO, ME ;
ABBONDANDOLO, A ;
FROSINA, G .
CARCINOGENESIS, 1995, 16 (09) :2267-2270
[9]  
Carter S K, 1972, Adv Cancer Res, V16, P273
[10]   SUBSTITUTED O-6-BENZYLGUANINE DERIVATIVES AND THEIR INACTIVATION OF HUMAN O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE [J].
CHAE, MY ;
MCDOUGALL, MG ;
DOLAN, ME ;
SWENN, K ;
PEGG, AE ;
MOSCHEL, RC .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (03) :342-347