Dou Dongwei, Ge Xin, Wang Xinxing, Xu Xiaodong, Zhang Zhe, Seng Jingjing, Cao Zhang, Gu Yuanting, Han Mingli
Department of Breast Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 475000, People's Republic of China.
Onco Targets Ther. 2019 Nov 13;12:9627-9637. doi: 10.2147/OTT.S214104. eCollection 2019.
Emerging evidence reveals the vital role of enhancer of zeste homolog 2 (EZH2) in cancer chemoresistance. However, its function and molecular mechanisms in breast cancer chemoresistance remain largely unknown.
Gene expression was evaluated using quantitative real-time PCR (qRT-PCR) and Western blot analysis. The functional roles of EZH2 and miR-381 in breast cancer were explored using cell MTT assay and flow cytometry analysis. The effect of EZH2 on miR-381 expression in transcriptional level was determined using Chromatin immunoprecipitation (ChIP) assay and Luciferase reporter assay.
In this study, we found that EZH2 was up-regulated in CDDP-resistant breast cancer tissues and cell lines. Breast cancer patients with high EZH2 expression had a poor prognosis. EZH2 silencing improved the sensitivity of MCF-7/CDDP and MDA-MB-231/CDDP cells towards CDDP. Moreover, EZH2 could epigenetically silence miR-381. miR-381 overexpression could overcome CDDP resistance in CDDP-resistant breast cancer cells. miR-381 knockdown weakened the inductive effect of EZH2 silencing on CDDP sensitivity of MCF-7/CDDP and MDA-MB-231/CDDP cells. Furthermore, EZH2 knockdown facilitated CDDP sensitivity of CDDP-resistant breast cancer cells in vivo.
Collectively, EZH2 depletion overcame CDDP resistance of breast cancer through epigenetically silencing miR-381, providing a novel therapeutic target for breast cancer chemoresistance.
新出现的证据揭示了zeste同源物2增强子(EZH2)在癌症化疗耐药性中的关键作用。然而,其在乳腺癌化疗耐药性中的功能和分子机制仍 largely未知。
使用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹分析评估基因表达。使用细胞MTT试验和流式细胞术分析探索EZH2和miR-381在乳腺癌中的功能作用。使用染色质免疫沉淀(ChIP)试验和荧光素酶报告基因试验确定EZH2在转录水平上对miR-381表达的影响。
在本研究中,我们发现EZH2在顺铂耐药的乳腺癌组织和细胞系中上调。EZH2高表达的乳腺癌患者预后较差。EZH2沉默提高了MCF-7/CDDP和MDA-MB-231/CDDP细胞对顺铂的敏感性。此外,EZH2可通过表观遗传沉默miR-381。miR-381过表达可克服顺铂耐药乳腺癌细胞中的顺铂耐药性。miR-381敲低减弱了EZH2沉默对MCF-7/CDDP和MDA-MB-231/CDDP细胞顺铂敏感性的诱导作用。此外,EZH2敲低促进了顺铂耐药乳腺癌细胞在体内对顺铂的敏感性。
总的来说,EZH2缺失通过表观遗传沉默miR-381克服了乳腺癌的顺铂耐药性,为乳腺癌化疗耐药性提供了一个新的治疗靶点。