Fram R J, Cusick P S, Marinus M G
Mutat Res. 1986 Jan;173(1):13-8. doi: 10.1016/0165-7992(86)90004-7.
Mutagenesis and cytotoxicity were studied in Escherichia coli by iproplatin and carboplatin, two analogs of cisplatin (CDDP) currently undergoing clinical trial. As with CDDP, mutagenesis by these agents was mediated by the umuDC gene product. In contrast to CDDP, however, mismatch repair did not substantially contribute to survival of cells after exposure to these agents since dam-3 E. coli were not more sensitive than wild type E. coli. UvrA- E. coli, however were more sensitive to these analogs demonstrating that as with CDDP, uvr endonuclease-mediated excision contributes to the repair of DNA damage induced by platinum compounds.
用异丙铂和卡铂这两种目前正在进行临床试验的顺铂(CDDP)类似物,在大肠杆菌中研究了诱变作用和细胞毒性。与CDDP一样,这些药物的诱变作用是由umuDC基因产物介导的。然而,与CDDP不同的是,错配修复对这些药物处理后细胞的存活没有实质性贡献,因为dam-3大肠杆菌并不比野生型大肠杆菌更敏感。然而,UvrA-大肠杆菌对这些类似物更敏感,这表明与CDDP一样,uvr核酸内切酶介导的切除有助于修复铂化合物诱导的DNA损伤。