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miR-188-5p通过靶向结肠癌细胞中的RASA1促进奥沙利铂耐药。

miR-188-5p promotes oxaliplatin resistance by targeting RASA1 in colon cancer cells.

作者信息

Zhu Xijia, Luo Xishun, Song Zhike, Jiang Shiyu, Long Xiangkai, Gao Xueyuan, Xie Xinyang, Zheng Laijian, Wang Haipeng

机构信息

Department of Gastrointestinal Surgery, The Second Affiliated Hospital of Guilin Medical University, Guilin, Guangxi Zhuang Autonomous Region 541199, P.R. China.

Department of Gastrointestinal Surgery, Guilin Medical University, Guilin, Guangxi Zhuang Autonomous Region 541004, P.R. China.

出版信息

Oncol Lett. 2021 Jun;21(6):481. doi: 10.3892/ol.2021.12742. Epub 2021 Apr 20.

Abstract

The efficacy of chemotherapy for colon cancer is limited due to the development of chemoresistance. MicroRNA (miR)-188-5p is downregulated in various types of cancer. The aim of the present study was to explore the molecular role of miR-188 in oxaliplatin (OXA) resistance. An OXA-resistant colon cancer cell line, SW480/OXA, was used to examine the effects of miR-188-5p on the sensitivity of colon cancer cells to OXA. The target of miR-188-5p was identified using a luciferase assay. Cell cycle distribution was also assessed using flow cytometry. The measurement of p21 protein expression, Hoechst 33342 staining and Annexin V/propidium iodide staining was used to evaluate apoptosis. The expression of miR-188-5p significantly increased in SW480/OXA compared with wild-type SW480 cells. The luciferase assay demonstrated that miR-188-5p inhibited Ras GTPase-activating protein 1 (RASA1; also known as p120/RasGAP) luciferase activity by binding to the 3'-untranslated region of RASA1 mRNA, suggesting that miR-188-5p could target RASA1. In addition, miR-188-5p downregulation or RASA1 overexpression promoted the chemosensitivity of SW480/OXA, as evidenced by increased apoptosis and G/S cell cycle arrest. Moreover, RASA1 silencing abrogated the increase in cell apoptosis induced by the miR-188-5p inhibitor. The findings of the present study suggested that miR-188-5p could enhance colon cancer cell chemosensitivity by promoting the expression of RASA1.

摘要

由于化疗耐药性的产生,结肠癌化疗的疗效有限。微小RNA(miR)-188-5p在多种类型癌症中表达下调。本研究旨在探讨miR-188在奥沙利铂(OXA)耐药中的分子作用。使用一种OXA耐药的结肠癌细胞系SW480/OXA来检测miR-188-5p对结肠癌细胞对OXA敏感性的影响。通过荧光素酶报告基因检测确定miR-188-5p的靶标。还使用流式细胞术评估细胞周期分布。通过检测p21蛋白表达、Hoechst 33342染色和膜联蛋白V/碘化丙啶染色来评估细胞凋亡。与野生型SW480细胞相比,SW480/OXA中miR-188-5p的表达显著增加。荧光素酶报告基因检测表明,miR-188-5p通过与RASA1 mRNA的3'非翻译区结合抑制Ras GTP酶激活蛋白1(RASA1;也称为p120/RasGAP)的荧光素酶活性,提示miR-188-5p可靶向RASA1。此外,miR-188-5p下调或RASA1过表达可促进SW480/OXA的化疗敏感性,细胞凋亡增加和G/S期细胞周期阻滞可证明这一点。此外,RASA1沉默消除了miR-188-5p抑制剂诱导的细胞凋亡增加。本研究结果提示,miR-188-5p可通过促进RASA1表达增强结肠癌细胞的化疗敏感性。

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