Bramson J, Panasci L C
Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital, Montreal, Quebec, Canada.
Cancer Res. 1993 Jul 15;53(14):3237-40.
Previous studies of ERCC-1 gene expression levels in chronic lymphocytic leukemia and ovarian carcinoma tumor specimens indicated that increased gene expression may correlate with a lack of response to the alkylating agents, melphalan, and cis-diamminedichloroplatinum (II). In order to demonstrate direct involvement of the ERCC-1 protein in repair of melphalan lesions, the ERCC-1 defective Chinese hamster ovary cell line UV20 was transfected with the human ERCC-1 complementary DNA. Stably transfected UV20 cells demonstrated an increase in resistance to melphalan. Wild type Chinese hamster ovary AA8 cells were then stably transfected with the same complementary DNA. The result was an increase in sensitivity to melphalan. There was no effect on sensitivity to uv light, but the ERCC-1 transfected AA8 cells had an increased sensitivity to cis-diamminedichloroplatinum (II). These results suggest that overexpression of human ERCC-1 may inhibit a pathway specific to the repair of bifunctional DNA damaging agent lesions in AA8 cells. ERCC-1 transfected AA8 cells should be useful in determining the precise role of ERCC-1 in repair of DNA cross-links induced by melphalan.
先前针对慢性淋巴细胞白血病和卵巢癌肿瘤标本中ERCC-1基因表达水平的研究表明,基因表达增加可能与对烷化剂美法仑和顺二氯二氨铂(II)缺乏反应相关。为了证明ERCC-1蛋白直接参与美法仑损伤的修复,将ERCC-1缺陷型中国仓鼠卵巢细胞系UV20用人类ERCC-1互补DNA进行转染。稳定转染的UV20细胞对美法仑的抗性增加。然后将野生型中国仓鼠卵巢AA8细胞用相同的互补DNA进行稳定转染。结果是对美法仑的敏感性增加。对紫外线敏感性没有影响,但ERCC-1转染的AA8细胞对顺二氯二氨铂(II)的敏感性增加。这些结果表明,人类ERCC-1的过表达可能抑制AA8细胞中双功能DNA损伤剂损伤修复的特定途径。ERCC-1转染的AA8细胞在确定ERCC-1在美法仑诱导的DNA交联修复中的精确作用方面应该是有用的。