Sylvester Cancer Center, University of Miami, FL, USA.
Anticancer Res. 2011 Nov;31(11):3757-66.
Patients with metastatic and muscle-invasive bladder cancer are commonly treated with cisplatin. A significant proportion of patients develop disease progression after an initial response to chemotherapy. Presently there is no standard of care for such patients. We examined whether pretreatment with an epigenetic agent would result in reversal of drug resistance.
Methylation of proapoptotic and cell cycle genes in bladder cancer cells was examined. Cisplatin- and docetaxel-resistant cells were generated. The effect of target of methylation-induced silencing (TMS1) expression and pretreatment of wild-type and drug-resistant cells with 5-azacytidine on chemosensitivity was determined.
Unidirectional crossresistance of cisplatin-resistant UMUC3 cells to docetaxel was observed. Recombinant expression of TMS1 or pre-treatment of wild-type and drug-resistant cells with 5-azacytidine resulted in enhanced sensitivity to cisplatin and docetaxel.
Our results indicate that epigenetic therapy may restore sensitivity to chemotherapeutic agents in bladder cancer cells.
转移性和肌层浸润性膀胱癌患者通常采用顺铂治疗。相当一部分患者在初始化疗反应后出现疾病进展。目前,此类患者尚无标准治疗方法。我们研究了预先使用表观遗传药物是否会导致耐药性逆转。
检测膀胱癌细胞中促凋亡和细胞周期基因的甲基化。生成顺铂和多西紫杉醇耐药细胞。检测 TMS1 表达的靶向和 5-氮杂胞苷预处理对野生型和耐药细胞的化疗敏感性的影响。
顺铂耐药 UMUC3 细胞对多西紫杉醇表现出单向交叉耐药性。TMS1 的重组表达或 5-氮杂胞苷预处理野生型和耐药细胞可增强对顺铂和多西紫杉醇的敏感性。
我们的结果表明,表观遗传学治疗可能恢复膀胱癌细胞对化疗药物的敏感性。