Roberts Elizabeth Gail, Vona-Davis Linda, Riggs Dale R, Jackson Barbara J, Hohseni Hesam, Kandzari Stanley J, McFadden David W
West Virginia University School of Medicine, Morgantown, USA.
W V Med J. 2004 May-Jun;100(3):96-101.
To test our hypothesis that Cyclooyxgenase-2 (COX-2) inhibitors would stop the growth of breast and prostate cancer cells in vitro, two breast (MCF-7, ZR75-1) and two prostate cancer cell lines (PC-3, DU145) were treated with rofecoxib (Vioxx) or NS398. Cell growth was measured by MTT at 24 and 72 hours. Statistical analysis was performed by ANOVA. Significant growth inhibition (p < 0.05) was observed in all cell lines in a dose-dependent manner after treatment with COX-2 inhibitors. Rofecoxib inhibited cellular proliferation by inducing (p < 0.001) apoptosis in breast cancer cells. Our study indicates that COX-2 inhibition reduces the growth of human breast and prostate cancer in vitro. Human studies are needed to evaluate the clinical utility of rofecoxib treatment in breast or prostate cancers.
为了验证我们的假设,即环氧化酶-2(COX-2)抑制剂会在体外抑制乳腺癌和前列腺癌细胞的生长,我们用罗非昔布(万络)或NS398处理了两种乳腺癌细胞系(MCF-7、ZR75-1)和两种前列腺癌细胞系(PC-3、DU145)。在24小时和72小时时通过MTT法测量细胞生长。采用方差分析进行统计分析。在用COX-2抑制剂处理后,所有细胞系均观察到显著的生长抑制(p<0.05),且呈剂量依赖性。罗非昔布通过诱导(p<0.001)乳腺癌细胞凋亡来抑制细胞增殖。我们的研究表明,COX-2抑制在体外可降低人乳腺癌和前列腺癌的生长。需要进行人体研究以评估罗非昔布治疗乳腺癌或前列腺癌的临床效用。