Bungo M, Fujiwara Y, Kasahara K, Nakagawa K, Ohe Y, Sasaki Y, Irino S, Saijo N
Pharmacology Division, National Cancer Center Research Institute, Tokyo, Japan.
Cancer Res. 1990 May 1;50(9):2549-53.
The mechanism of resistance to cis-diamminedichloroplatinum(II) (CDDP) is still controversial, although several kinds of processes have been proposed. For elucidation of the mechanism of CDDP resistance in CDDP-resistant human non-small cell lung cancer cells (PC-9/0.5, 7.1-fold resistant), we examined the formation of DNA interstrand cross-links (ICL), one kind of DNA damage induced by CDDP, its repair, and intracellular accumulation of CDDP. We measured the frequency of CDDP-induced ICL by means of the alkaline elution technique and the amount of intracellular platinum for intracellular accumulation of CDDP by means of atomic absorption spectrophotometry in PC-9 (parental cell) and PC-9/0.5 cells. Formation of ICL in PC-9 cells exposed to 5 micrograms of CDDP per ml for 6 h was 5.85 times that in PC-9/0.5 cells. On the other hand, the ability to repair CDDP-induced ICL was identical in both cell lines. Intracellular accumulation studies revealed that PC-9 retained 5.07 times as much platinum as that in PC-9/0.5 after 3-h exposure to CDDP. It was conjectured that the decrease in the intracellular accumulation of CDDP might be the main cause of CDDP resistance in PC-9 cells, since the decreased accumulation was paralleled by the decreased level of ICL.
尽管已经提出了几种过程,但顺二氨二氯铂(II)(CDDP)的耐药机制仍存在争议。为了阐明耐CDDP的人非小细胞肺癌细胞(PC-9/0.5,耐药7.1倍)中CDDP耐药的机制,我们研究了DNA链间交联(ICL)的形成,ICL是CDDP诱导的一种DNA损伤、其修复以及CDDP的细胞内积累情况。我们通过碱性洗脱技术测量了CDDP诱导的ICL频率,并通过原子吸收分光光度法测量了PC-9(亲代细胞)和PC-9/0.5细胞中CDDP细胞内积累的细胞内铂含量。每毫升暴露于5微克CDDP 6小时的PC-9细胞中ICL的形成是PC-9/0.5细胞中的5.85倍。另一方面,两种细胞系修复CDDP诱导的ICL的能力相同。细胞内积累研究表明,暴露于CDDP 3小时后,PC-9保留的铂是PC-9/0.5中的5.07倍。据推测,CDDP细胞内积累的减少可能是PC-9细胞中CDDP耐药的主要原因,因为积累的减少与ICL水平的降低平行。