Tsai C M, Gazdar A F, Allegra C, Perng R P, Kramer B S
Chest Department, Veterans General Hospital, Taipei, Taiwan, Republic of China.
Int J Cancer. 1990 Jul 15;46(1):101-5. doi: 10.1002/ijc.2910460119.
Reduced folates have been shown to increase the cytotoxicity of 5-fluorouracil (FUra) by stabilizing the fluorodeoxyuridine monophosphate:thymidylate synthase complex, thus increasing the block in the DNA synthetic pathway. Using an in vitro tetrazolium colorimetric (MTT) cytotoxic assay, we tested the effects of FUra and 5-fluorodeoxyuridine (FUdR) with and without leucovorin (LV) on a panel of 7 human lung cancer cell lines. LV at a concentration of 20 microM enhanced the cytotoxicity of FUra and of FUdR in all of the cell lines. Quantitatively, LV had a higher degree of enhancement on FUdR than on FUra cytotoxicity in 6 cell lines. There was equivalent enhancement in the only remaining line. The differential effects of LV on the cytotoxicity of FUra vs. FUdR in these lung carcinoma lines contrasts with a quantitatively similar enhancement of cytotoxicity between FUra and FUdR in colon cancer lines previously reported from our laboratory. This suggests that the metabolism of FUra may be different in these lung cancer cell lines.
胸苷酸合成酶复合物来增加5-氟尿嘧啶(FUra)的细胞毒性,从而增强DNA合成途径中的阻断作用。我们使用体外四唑盐比色法(MTT)细胞毒性试验,检测了有或没有亚叶酸(LV)存在时,FUra和5-氟脱氧尿苷(FUdR)对一组7种人肺癌细胞系的影响。浓度为20微摩尔的LV增强了所有细胞系中FUra和FUdR的细胞毒性。定量分析表明,在6种细胞系中,LV对FUdR细胞毒性的增强程度高于对FUra的增强程度。在剩下的唯一一个细胞系中,增强效果相同。LV对这些肺癌细胞系中FUra与FUdR细胞毒性的不同影响,与我们实验室之前报道的结肠癌细胞系中FUra和FUdR细胞毒性在数量上相似的增强情况形成对比。这表明这些肺癌细胞系中FUra的代谢可能有所不同。