Suppr超能文献

EZH2通过表观遗传抑制miR-381表达促进乳腺癌顺铂耐药。

EZH2 Contributes To Cisplatin Resistance In Breast Cancer By Epigenetically Suppressing miR-381 Expression.

作者信息

Dou Dongwei, Ge Xin, Wang Xinxing, Xu Xiaodong, Zhang Zhe, Seng Jingjing, Cao Zhang, Gu Yuanting, Han Mingli

机构信息

Department of Breast Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 475000, People's Republic of China.

出版信息

Onco Targets Ther. 2019 Nov 13;12:9627-9637. doi: 10.2147/OTT.S214104. eCollection 2019.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

Collectively, EZH2 depletion overcame CDDP resistance of breast cancer through epigenetically silencing miR-381, providing a novel therapeutic target for breast cancer chemoresistance.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b61/6859472/ce0da2d7877a/OTT-12-9627-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验