Quinn Jennifer E, James Colin R, Stewart Gail E, Mulligan Jude M, White Patricia, Chang Gary K F, Mullan Paul B, Johnston Patrick G, Wilson Richard H, Harkin D Paul
Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
Clin Cancer Res. 2007 Dec 15;13(24):7413-20. doi: 10.1158/1078-0432.CCR-07-1083.
We investigated whether BRCA1 mRNA expression levels may represent a biomarker of survival in sporadic epithelial ovarian cancer following chemotherapy treatment.
The effect of loss of BRCA1 expression on chemotherapy response in ovarian cancer was measured in vitro using dose inhibition assays and Annexin V flow cytometry. Univariate and multivariate analyses were done to evaluate the relationship between BRCA1 mRNA expression levels and survival after chemotherapy treatment in 70 fresh frozen ovarian tumors.
We show that inhibition of endogenous BRCA1 expression in ovarian cancer cell lines results in increased sensitivity to platinum therapy and decreased sensitivity to antimicrotubule agents. In addition, we show that patients with low/intermediate levels of BRCA1 mRNA have a significantly improved overall survival following treatment with platinum-based chemotherapy in comparison with patients with high levels of BRCA1 mRNA (57.2 versus 18.2 months; P = 0.0017; hazard ratio, 2.9). Furthermore, overall median survival for higher-BRCA1-expressing patients was found to increase following taxane-containing chemotherapy (23.0 versus 18.2 months; P = 0.12; hazard ratio, 0.53).
We provide evidence to support a role for BRCA1 mRNA expression as a predictive marker of survival in sporadic epithelial ovarian cancer.
我们研究了BRCA1 mRNA表达水平是否可作为散发性上皮性卵巢癌化疗后生存的生物标志物。
使用剂量抑制试验和膜联蛋白V流式细胞术在体外测量BRCA1表达缺失对卵巢癌化疗反应的影响。对70例新鲜冷冻卵巢肿瘤进行单因素和多因素分析,以评估BRCA1 mRNA表达水平与化疗后生存之间的关系。
我们发现,抑制卵巢癌细胞系中内源性BRCA1表达会导致对铂类疗法的敏感性增加,而对抗微管药物的敏感性降低。此外,我们发现,与BRCA1 mRNA高水平的患者相比,BRCA1 mRNA低/中等水平的患者接受铂类化疗后的总生存期显著改善(57.2个月对18.2个月;P = 0.0017;风险比,2.9)。此外,发现接受含紫杉烷化疗后,BRCA1表达较高患者的总体中位生存期有所增加(23.0个月对18.2个月;P = 0.12;风险比,0.53)。
我们提供证据支持BRCA1 mRNA表达作为散发性上皮性卵巢癌生存预测标志物的作用。