Huang Xiaoting, Xiang Leyang, Wang Baiyao, Hu Jijie, Liu Chunshan, Ren Anbang, Du Kunpeng, Ye Gengtai, Liang Yingying, Tang Yunqiang, Yang Dinghua, Yuan Yawei
Department of Radiation Oncology, Affiliated Cancer Hospital & Institute of Guangzhou Medical University, No. 78 Hengzhigang Road, Guangzhou, 510095, Guangdong, People's Republic of China.
State Key Laboratory of Respiratory Diseases, Guangzhou Institute of Respiratory Disease, Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.
J Transl Med. 2021 Mar 23;19(1):120. doi: 10.1186/s12967-021-02787-5.
CKLF like MARVEL transmembrane domain containing 6 (CMTM6) has been associated with the development in many kinds of cancers. However, the roles of CMTM6 in hepatocellular carcinoma (HCC) are largely unknown. Thus, the present study aimed to investigate the function of CMTM6 in HCC.
We analysed CMTM6 levels and functions using human HCC cell lines, paired HCC and adjacent non-tumorous tissues, and a tissue microarray. CMTM6 expression was silenced using short hairpin RNAs and its was overexpressed from a lentivirus vector. CMTM6 mRNA and protein levels were determined using quantitative real-time reverse transcription PCR and western blotting, respectively. Proliferation, colony formation, migration, and invasion were assessed using a Cell counting kit-8, colony formation, wound-healing, and Matrigel invasion assays, respectively. Immunohistochemistry was used to score the expression of CMTM6 in tissue samples. The localization and binding partners of CMTM6 were investigated using immunofluorescence and coimmunoprecipitation experiments, respectively. A mouse xenograft model was used for in vivo studies.
Compared with that in adjacent, non-cancerous tissue, Here, CMTM6 levels were increased in HCC tissue samples. Silencing of CMTM6 suppressed the proliferation, migration, and invasion of HCC cells. Conversely, CMTM6 overexpression enhanced HCC cell invasion, migration, and proliferation. Mechanistically, CMTM6 physically interacts with and stabilizes vimentin, thus inducing epithelial-mesenchymal transition (EMT), which promotes proliferation, migration and invasion. Importantly, in HCC tissues, CMTM6 expression correlated positively with vimentin levels. Poor prognosis of HCC was associated significantly with higher CMTM6 expression.
CMTM6 has an important function in HCC proliferation, migration, and invasion, via its interaction with and stabilization of vimentin. CMTM6 might represent a potential biomarker and therapeutic target to treat HCC.
含MARVEL跨膜结构域的CKLF样蛋白6(CMTM6)与多种癌症的发生发展相关。然而,CMTM6在肝细胞癌(HCC)中的作用尚不清楚。因此,本研究旨在探讨CMTM6在HCC中的功能。
我们使用人HCC细胞系、配对的HCC组织和癌旁非肿瘤组织以及组织芯片分析CMTM6的水平和功能。使用短发夹RNA沉默CMTM6表达,并通过慢病毒载体使其过表达。分别使用定量实时逆转录PCR和蛋白质印迹法测定CMTM6的mRNA和蛋白质水平。分别使用细胞计数试剂盒-8、集落形成、伤口愈合和基质胶侵袭试验评估细胞增殖、集落形成、迁移和侵袭能力。免疫组织化学用于对组织样本中CMTM6的表达进行评分。分别使用免疫荧光和免疫共沉淀实验研究CMTM6的定位和结合伙伴。使用小鼠异种移植模型进行体内研究。
与癌旁非癌组织相比,HCC组织样本中CMTM6水平升高。沉默CMTM6可抑制HCC细胞的增殖、迁移和侵袭。相反,CMTM6过表达增强了HCC细胞的侵袭、迁移和增殖。机制上,CMTM6与波形蛋白发生物理相互作用并使其稳定,从而诱导上皮-间质转化(EMT),促进增殖、迁移和侵袭。重要的是,在HCC组织中,CMTM6表达与波形蛋白水平呈正相关。HCC患者预后不良与CMTM6高表达显著相关。
CMTM6通过与波形蛋白相互作用并使其稳定,在HCC增殖、迁移和侵袭中发挥重要作用。CMTM6可能是治疗HCC的潜在生物标志物和治疗靶点。