Joseph P, Sharma M C, Jaiswal A K
Department of Pharmacology, Fox Chase Cancer Center, Philadelphia, PA 19111.
Biochem Pharmacol. 1994 Jun 1;47(11):2011-5. doi: 10.1016/0006-2952(94)90076-0.
Human colon carcinoma HT29 cells sensitive (WT) and resistant (HT/M and HT/S) to ethacrynic acid (EA) were used to investigate the role of NAD(P)H:quinone oxidoreductase1 (NQO1) in drug resistance. Significant decreases in the levels of NQO1 activity were observed in resistant cells as compared with the sensitive cells. However, the decreased activities of NQO1 in resistant cells were found to be due to inhibition of the enzyme by EA. Human NQO1 cDNA-derived protein in monkey kidney COS1 cell extract was used to demonstrate that in vitro inhibition of NQO1 activity by EA was rapid, reversible and concentration dependent, with an IC50 value of 250 microM. These results suggest that NQO1 may not have a role in EA resistance of human colon carcinoma HT29 cells and that EA is an inhibitor of NQO1 activity.
利用对依他尼酸(EA)敏感(WT)和耐药(HT/M和HT/S)的人结肠癌HT29细胞,研究烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H):醌氧化还原酶1(NQO1)在耐药中的作用。与敏感细胞相比,耐药细胞中NQO1活性水平显著降低。然而,发现耐药细胞中NQO1活性降低是由于EA对该酶的抑制作用。用猴肾COS1细胞提取物中的人NQO1 cDNA衍生蛋白证明,EA对NQO1活性的体外抑制作用迅速、可逆且浓度依赖性,IC50值为250微摩尔。这些结果表明,NQO1可能在人结肠癌HT29细胞的EA耐药中不起作用,且EA是NQO1活性的抑制剂。