Pretreatment with 5-fluorouracil enhances cytotoxicity and retention of DNA-bound platinum in a cisplatin resistant human ovarian cancer cell line

Citation
T. Tanaka et al., Pretreatment with 5-fluorouracil enhances cytotoxicity and retention of DNA-bound platinum in a cisplatin resistant human ovarian cancer cell line, ANTICANC R, 21(4A), 2001, pp. 2463-2469
Citations number
39
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
21
Issue
4A
Year of publication
2001
Pages
2463 - 2469
Database
ISI
SICI code
0250-7005(200107/08)21:4A<2463:PW5ECA>2.0.ZU;2-3
Abstract
A combination of 5-fluorouracil (5-FU) and cisplatin (cis-Diamminedichlorop latinum(II); CDDP) was administered to CDDP-sensitive (A2780) and -resistan t (2780(CP)) human ovarian cancer cell lines in vitro in order to investiga te the effects of 5-FU pretreatment on CDDP cytotoxicity, removal of DNA-bo und platinum (Pt-DNA) and cellular glutathione (GSH) level. The cells were incubated with various doses of 5-FU for 24 hours, and then exposed to vari ous doses of CDDP after a drug-free interval of 24 hours. Pretreatment with 5-FU (0.5 - 2.0 mug/ml) augmented the cytotoxicity of CDDP in 2780(CP) cel ls, but did not affect A2780 cells. 2780(CP) cells lost 23.0 to 41.9% of th eir total Pt-DNA determined by flameless atomic absorption spectrophotometr y at 6 to 24 hours after exposure to 10.0 mug/ml CDDP alone; nevertheless, 1.0 mug/ml 5-FU pretreatment caused a significant delay in removal of Pt-DN A (3.8, 1.5 and 7.2% at 6, 12 and 24 hours after exposure to CDDP, respecti vely). At 24 hours after 15.0 mug/ml CDDP exposure, 2780CP cells pretreated with 5-FU lost only 15.7% of their total Pt-DNA, although the platinum rem oval rate with CDDP alone was 28.4%. The GSH levels in 2780(CP) cells were similar in the presence or absence of 5-FU pretreatment. These data indicat ed that 5-FU pretreatment enhances the cytotoxicity of CDDP and reverses CD DP resistance in 2780(CP) cells and that its mechanism is related to the in hibitory effect of 5-FU on DNA repair, and not to cellular GSH levels.