Hypersensitivity in DNA mismatch repair-deficient colon carcinoma cells to DNA polymerase reaction inhibitors

被引:17
作者
Takahashi, T
Min, Z
Uchida, L
Arita, M
Watanabe, Y
Koi, M
Hemmi, H
机构
[1] Toho Univ, Fac Med, Dept Biol Mol, Ohta Ku, Tokyo 1438540, Japan
[2] Kinki Univ, Sch Med, Dept Obstet & Gynecol, Osaka, Japan
[3] Brunel Univ, Dept Sci Biol, Brunel Inst Canc Genet & Pharmacogenom, Uxbridge UB8 3PH, Middx, England
基金
日本学术振兴会;
关键词
DNA mismatch repair; colon carcinoma; DNA polymerase; DNA replication; hypersensitive;
D O I
10.1016/j.canlet.2004.07.044
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We studied the cytotoxic effects of various DNA replication inhibitors on MMR-deficient and -proficient colon carcinoma cell lines. DNA polymerase (pol) inhibitors including aphidicolin and gemcitabine, and hydroxyurea were more toxic (1.7 to 2.8-fold) to hMLH1-deficient HCT116 than to hMLH1-proficient HCT116+ch3. Similarly, pol inhibitors were more toxic to hMSH2-deficient LoVo than to hMSH2-proficient LoVo + ch2. In contrast, DNA topoisomerase I inhibitors, such as CPT-11, SN-38, and topotecan, were more toxic to MMR-proficient cells. Our results suggest that NINIR-deficient colon carcinoma cells are hypersensitive to inhibitors of the pol reaction. (c) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:85 / 93
页数:9
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