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跨膜蛋白166通过上调TP53抑制肝癌细胞的增殖、迁移和侵袭。

TMEM166 inhibits cell proliferation, migration and invasion in hepatocellular carcinoma via upregulating TP53.

作者信息

Yang Jiejie, Wang Bin, Xu Qian, Yang Yuling, Hou Lin, Yin Kan, Guo Qingming, Hua Yanan, Zhang Li, Li Yixuan, Zhang Jinyu, Li Ning

机构信息

Department of Biochemistry and Molecular Biology, School of Basic Medicine, Qingdao University, Qingdao, 266071, China.

School of Electronic Information, Qingdao University, Qingdao, 266071, China.

出版信息

Mol Cell Biochem. 2021 Feb;476(2):1151-1163. doi: 10.1007/s11010-020-03979-1. Epub 2020 Nov 16.

DOI:10.1007/s11010-020-03979-1
PMID:33200377
Abstract

Transmembrane protein 166 (TMEM166), an endoplasmic reticulum-associated protein, functions in many diseases via regulating autophagy and/or apoptosis. However, the role of TMEM166 in hepatocellular carcinoma (HCC) remains largely unknown. In this study, we detected the expression of TMEM166 in HCC by real-time fluorescent quantitative PCR (RT-qPCR), immunohistochemistry and western blot. To investigate its biological function and underlying mechanism in HCC, TMEM166 was overexpressed in HCC cell lines and assessed its effects on cell proliferation, migration, invasion, apoptosis and cell cycle by MTT assay, wound healing assay, Transwell assay, Annexin V-FITC/PI assay, JC-1 staining and flow cytometry assay, respectively. Results demonstrated that the expression of TMEM166 was significantly decreased in HCC and was associated with advanced TNM clinical stage and poor clinical outcome of HCC patients. TMEM166 overexpression inhibited HCC cells proliferation, migration and invasion. Furthermore, TMEM166 inhibited cell proliferation by inducing apoptosis and cell cycle arrest via upregulating anti-oncogene TP53 and TP53 knockdown significantly alleviated the anti-tumor effects of TMEM166 on HCC cells. This study provides the first comprehensive analysis the role of TMEM166 in HCC. TMEM166 displays a fine anti-tumor activity on HCC cells involving a mechanism of upregulating TP53. This study suggests TMEM166 is a potential target for the treatment of HCC.

摘要

跨膜蛋白166(TMEM166)是一种内质网相关蛋白,通过调节自噬和/或凋亡在多种疾病中发挥作用。然而,TMEM166在肝细胞癌(HCC)中的作用仍 largely未知。在本研究中,我们通过实时荧光定量PCR(RT-qPCR)、免疫组织化学和蛋白质印迹法检测了HCC中TMEM166的表达。为了研究其在HCC中的生物学功能和潜在机制,在HCC细胞系中过表达TMEM166,并分别通过MTT法、伤口愈合试验、Transwell试验、膜联蛋白V-FITC/PI试验、JC-1染色和流式细胞术试验评估其对细胞增殖、迁移、侵袭、凋亡和细胞周期的影响。结果表明,TMEM166的表达在HCC中显著降低,且与HCC患者的晚期TNM临床分期和不良临床预后相关。TMEM166过表达抑制了HCC细胞的增殖、迁移和侵袭。此外,TMEM166通过上调抑癌基因TP53诱导凋亡和细胞周期停滞来抑制细胞增殖,TP53基因敲低显著减轻了TMEM166对HCC细胞的抗肿瘤作用。本研究首次全面分析了TMEM166在HCC中的作用。TMEM166对HCC细胞显示出良好的抗肿瘤活性,其机制涉及上调TP53。本研究表明TMEM166是治疗HCC的潜在靶点。

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