Department of Epidemiology and Public Health, Yale Cancer Center, Yale University School of Medicine, New Haven, CT 06520-8034, USA.
Gynecol Oncol. 2011 Aug;122(2):366-71. doi: 10.1016/j.ygyno.2011.04.033. Epub 2011 May 14.
Let-7 is a family of small non-coding RNAs regulating the expression of many genes that control important cellular activities. Let-7 is shown in vitro to sensitize cancer cells to platinum, but induce ovarian cancer resistance to paclitaxel. This study aims to investigate the effect of let-7a expression on survival outcomes of epithelial ovarian cancer (EOC) patients treated with different chemotherapy.
Let-7a expression was measured with qRT-PCR in ovarian tumors of 178 EOC patients who received platinum-based chemotherapy with and without paclitaxel after surgery. Survival analysis was performed to assess the effects of let-7a and chemotherapy on disease outcomes.
Let-7a expression was detectable in the EOC samples, but the expression was not associated with disease stage, tumor grade, histology and debulking results. Patients who responded to platinum with paclitaxel had significantly lower let-7a than those who did not. Survival analyses showed that patients with high let-7a had better survival compared to those with low let-7a when they were treated with platinum without paclitaxel. The hazards ratios (HRs) for death and disease progression were 0.52 (95% CI: 0.29-0.96) and 0.48 (0.26-0.89) for high let-7a when compared to low let-7a, respectively. However, when patients were treated with platinum and paclitaxel, high let-7a was associated with worse progression-free and overall survival. The HRs for death and disease progression were 3.87 (95% CI: 1.28-11.66) and 3.48 (95% CI: 1.25-9.67) for high let-7a when compared to low let-7a, respectively. Further studies showed that among patients with low let-7a, those treated with paclitaxel in addition to platinum survived better than those treated without paclitaxel [adjusted-HRs were 0.31 (95% CI: 0.15-0.66) for death and 0.40 (95% CI: 0.22-0.75) for disease], while among those with high let-7a, the two types of treatment made no difference in patient survival.
The study suggests that the beneficial impact of the addition of paclitaxel on EOC survival was significantly linked to let-7a levels, and that miRNAs such as let-7a may be a useful marker for selection of chemotherapeutic agents in EOC management.
Let-7 是一组调节许多控制重要细胞活动的基因表达的小非编码 RNA。体外研究表明,Let-7 可使癌细胞对铂类药物敏感,但诱导卵巢癌对紫杉醇产生耐药性。本研究旨在探讨 Let-7a 表达对接受不同化疗的上皮性卵巢癌 (EOC) 患者生存结局的影响。
对 178 例 EOC 患者的卵巢肿瘤进行 qRT-PCR 检测 Let-7a 的表达,这些患者在手术后接受了铂类联合紫杉醇化疗或铂类单药化疗。进行生存分析以评估 Let-7a 和化疗对疾病结局的影响。
EOC 样本中可检测到 Let-7a 的表达,但表达与疾病分期、肿瘤分级、组织学和减瘤结果无关。对铂类联合紫杉醇有反应的患者 Let-7a 表达明显低于无反应者。生存分析显示,与低 Let-7a 组相比,高 Let-7a 组在接受铂类单药治疗时的生存情况更好。高 Let-7a 组的死亡和疾病进展风险比 (HR) 分别为 0.52 (95%CI: 0.29-0.96) 和 0.48 (0.26-0.89)。然而,当患者接受铂类联合紫杉醇治疗时,高 Let-7a 与无进展生存期和总生存期较差相关。高 Let-7a 组的死亡和疾病进展 HR 分别为 3.87 (95%CI: 1.28-11.66) 和 3.48 (95%CI: 1.25-9.67)。进一步的研究表明,在低 Let-7a 患者中,与未接受紫杉醇治疗的患者相比,接受紫杉醇联合铂类治疗的患者的生存情况更好 [死亡的校正 HR 为 0.31 (95%CI: 0.15-0.66),疾病进展的校正 HR 为 0.40 (95%CI: 0.22-0.75)],而在高 Let-7a 患者中,两种治疗方式对患者生存无差异。
本研究表明,紫杉醇的添加对 EOC 生存的有益影响与 Let-7a 水平显著相关,miRNAs 如 Let-7a 可能是上皮性卵巢癌管理中选择化疗药物的有用标志物。