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Circ_0007142吸附miR-647调控CCR8基因促进胃癌细胞的上皮-间质转化和侵袭
引用本文:张学成,关晓辉. Circ_0007142吸附miR-647调控CCR8基因促进胃癌细胞的上皮-间质转化和侵袭[J]. 中国癌症杂志, 2021, 31(8): 714-724. DOI: 10.19401/j.cnki.1007-3639.2021.08.004
作者姓名:张学成  关晓辉
作者单位:1. 吉林市中心医院消化科,吉林 吉林 132000 ;2. 北华大学附属医院消化内科,吉林 吉林 132000
基金项目:吉林省卫生厅科技计划项目(2013S004)。
摘    要:背景与目的:胃癌是常见的消化道恶性肿瘤,circ_0007142被证实为结直肠癌的致癌因子,能促进结直肠癌的进展.探究circ_0007142吸附miR-647调控CCR8基因对胃癌细胞上皮-间质转化(epithelial-mesenchymal transition,EMT)和侵袭的影响.方法:采用实时荧光定量聚合酶...

关 键 词:Circ_0007142  miR-647  CCR8  胃癌  上皮-间质转化  侵袭

Circ_0007142 accelerates epithelial-mesenchymal transition and invasion of gastric cancer cells through sponging miR-647 and regulating CCR8 gene
ZHANG Xuecheng,GUAN Xiaohui. Circ_0007142 accelerates epithelial-mesenchymal transition and invasion of gastric cancer cells through sponging miR-647 and regulating CCR8 gene[J]. China Oncology, 2021, 31(8): 714-724. DOI: 10.19401/j.cnki.1007-3639.2021.08.004
Authors:ZHANG Xuecheng  GUAN Xiaohui
Affiliation:1. Department of Gastroenterology, Beihua University, Jilin Central Hospital, Jilin 132000, Jilin Province, China; 2. Department of Gastroenterology, Affiliated Hospital of Beihua University, Jilin 132000, Jilin Province, China;
Abstract:Background and purpose: Gastric cancer is the most common malignant tumor of digestive tract. Circ_0007142 has been proved to be a carcinogenic factor of colorectal cancer and can promote the progression of colorectal cancer. This study aimed to explore the effects of circ_0007142 on epithelial-mesenchymal transition (EMT) and invasion of gastric cancer cells via absorbing miR-647 and then regulating CCR8 gene. Methods: Real-time fluorescence quantitative polymerase chain reaction (RTFQ-PCR) was used to detect the expressions of circ_0007142, miR-647 and CCR8 in gastric cancer tissues and cells. Fluorescence in situ hybridization (FISH) experiment was adopted to determine the subcellular localization of circ_0007142. Dual luciferase reporter experiment and RNA immunoprecipitation (RIP) assay were used to confirm the targeting relationship of circ_0007142 and miR-647 as well as miR-647 and CCR8. Transwell assay, clone formation assay and Western blot were used to test the cell invasion ability, clonality and EMT respectively. Tumor xenograft in BALB/c nude mice was performed to detect tumorigenicity of circ_0007142 in vivo. Results: Overexpressions of circ_0007142 and CCR8 and downregulation of miR-647 were detected in gastric cancer tissues and cells. Circ_0007142 acted as a molecular sponge to inhibit the expression of miR-647, at the same time, miR-647 inhibited theexpression of CCR8 by binding with the 3'-UTR of CCR8 mRNA. Knockdown of circ_0007142 or overexpression of miR-647 inhibited the invasion, colony formation and EMT of gastric cancer cells. However, the effects of circ_0007142 inhibition or miR-647 overexpression on gastric cancer cells were partially reversed by miR-647 inhibitor or CCR8 overexpression (all P<0.05). Moreover, knockdown of circ_0007142 in gastric cancer cells inhibited the tumor growth in vivo. Conclusion: Circ_0007142 upregulates the expression of CCR8 via sponging miR-647, which subsequently accelerates the EMT and invasion of gastric cancer cells and promotes the progression of gastric cancer.
Keywords:Circ_0007142   miR-647   CCR8   Gastric cancer   Epithelial-mesenchymal transition   Invasion  
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