Bao Lingjie, Wu Jianfa, Dodson Matthew, Rojo de la Vega Elisa Montserrat, Ning Yan, Zhang Zhenbo, Yao Ming, Zhang Donna D, Xu Congjian, Yi Xiaofang
Department of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, Shanghai, China.
Mol Carcinog. 2017 Jun;56(6):1543-1553. doi: 10.1002/mc.22615. Epub 2017 May 2.
Previously, we have demonstrated that NRF2 plays a key role in mediating cisplatin resistance in ovarian cancer. To further explore the mechanism underlying NRF2-dependent cisplatin resistance, we stably overexpressed or knocked down NRF2 in parental and cisplatin-resistant human ovarian cancer cells, respectively. These two pairs of stable cell lines were then subjected to microarray analysis, where we identified 18 putative NRF2 target genes. Among these genes, ABCF2, a cytosolic member of the ABC superfamily of transporters, has previously been reported to contribute to chemoresistance in clear cell ovarian cancer. A detailed analysis on ABCF2 revealed a functional antioxidant response element (ARE) in its promoter region, establishing ABCF2 as an NRF2 target gene. Next, we investigated the contribution of ABCF2 in NRF2-mediated cisplatin resistance using our stable ovarian cancer cell lines. The NRF2-overexpressing cell line, containing high levels of ABCF2, was more resistant to cisplatin-induced apoptosis compared to its control cell line; whereas the NRF2 knockdown cell line with low levels of ABCF2, was more sensitive to cisplatin treatment than its control cell line. Furthermore, transient overexpression of ABCF2 in the parental cells decreased apoptosis and increased cell viability following cisplatin treatment. Conversely, knockdown of ABCF2 using specific siRNA notably increased apoptosis and decreased cell viability in cisplatin-resistant cells treated with cisplatin. This data indicate that the novel NRF2 target gene, ABCF2, plays a critical role in cisplatin resistance in ovarian cancer, and that targeting ABCF2 may be a new strategy to improve chemotherapeutic efficiency.
此前,我们已经证明NRF2在介导卵巢癌顺铂耐药中起关键作用。为了进一步探究NRF2依赖性顺铂耐药的潜在机制,我们分别在亲本和顺铂耐药的人卵巢癌细胞中稳定过表达或敲低NRF2。然后对这两对稳定细胞系进行微阵列分析,在此过程中我们鉴定出18个假定的NRF2靶基因。在这些基因中,ABCF2是转运蛋白ABC超家族的胞质成员,此前有报道称其有助于透明细胞卵巢癌的化疗耐药。对ABCF2的详细分析揭示了其启动子区域存在一个功能性抗氧化反应元件(ARE),从而确定ABCF2为NRF2靶基因。接下来,我们使用稳定的卵巢癌细胞系研究了ABCF2在NRF2介导的顺铂耐药中的作用。与对照细胞系相比,过表达NRF2的细胞系含有高水平的ABCF2,对顺铂诱导的凋亡更具抗性;而敲低NRF2的细胞系中ABCF2水平较低,对顺铂治疗比其对照细胞系更敏感。此外,在亲本细胞中瞬时过表达ABCF2可减少顺铂处理后的凋亡并提高细胞活力。相反,在用顺铂处理的顺铂耐药细胞中,使用特异性siRNA敲低ABCF2可显著增加凋亡并降低细胞活力。这些数据表明,新的NRF2靶基因ABCF2在卵巢癌顺铂耐药中起关键作用,靶向ABCF2可能是提高化疗效率的新策略。