Qin Yuping, Cao Tong, Xu Ying, Jiang Xu, Ma Jia, Yu Li
Key Laboratory of Cancer Research and Clinical Laboratory Diagnosis, Bengbu Medical College, Bengbu 233000, China.
Key Laboratory of Cancer Research and Clinical Laboratory Diagnosis, Department of Transfusion, School of Laboratory Medicine, Bengbu Medical College, Bengbu 233000, China. *Corresponding author, E-mail:
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2023 Mar;39(3):249-257.
Objective To investigate the effect of calcium voltage gated channel subunit α 1C antisense RNA2 (CACNA1C-AS2) on malignant biological characteristics of esophageal cancer cells by regulating epithelial mesenchymal transition (EMT). Methods CACNA1C-AS2 expression levels in paracancerous tissues and esophageal cancer tissues were analyzed by TCGA database. Real-time quantitative PCR was used to detect the expression of CACNA1C-AS2 mRNA in esophageal cancer cells. Following the knockdown and high expression of CACNA1C-AS2 in esophageal cancer cells, the viability of the cells was tested by MTT assay and cell colony formation assay. Transwell chamber method was used to measure the invasion and longitudinal migration of the cells. The horizontal migration ability of the cells was evaluated by wound healing test. The apoptosis rates of cells were detected by flow cytometry. Western blot analysis was used to detect the expressions of N-cadherin, vimentin and slug. Results CACNA1C-AS2 expression levels were low in esophageal cancer tissues and cell lines. After knocking down the expression of CACNA1C-AS2 in EC-9706 cells and Eca-109 cells, the ability of invasion and migration and viability of esophageal cancer cells were significantly enhanced, and the apoptosis rates were decreased, while the expressions of N-cadherin, vimentin and slug were up-regulated. However, the results are opposite via the over-expression of CACNA1C-AS2. Conclusion CACNA1C-AS2 enhances the proliferation, invasion and migration of esophageal cancer cells by promoting EMT.
目的 通过调节上皮间质转化(EMT)来研究钙电压门控通道亚基α1C反义RNA2(CACNA1C-AS2)对食管癌细胞恶性生物学特性的影响。方法 利用TCGA数据库分析癌旁组织和食管癌组织中CACNA1C-AS2的表达水平。采用实时定量PCR检测食管癌细胞中CACNA1C-AS2 mRNA的表达。在食管癌细胞中敲低和高表达CACNA1C-AS2后,通过MTT法和细胞集落形成试验检测细胞活力。采用Transwell小室法测定细胞的侵袭和纵向迁移能力。通过伤口愈合试验评估细胞的横向迁移能力。采用流式细胞术检测细胞凋亡率。用蛋白质免疫印迹法检测N-钙黏蛋白、波形蛋白和蛞蝓蛋白的表达。结果 食管癌组织和细胞系中CACNA1C-AS2表达水平较低。在EC-9706细胞和Eca-109细胞中敲低CACNA1C-AS2的表达后,食管癌细胞的侵袭、迁移能力和活力显著增强,凋亡率降低,而N-钙黏蛋白、波形蛋白和蛞蝓蛋白的表达上调。然而,过表达CACNA1C-AS2时结果相反。结论 CACNA1C-AS2通过促进EMT增强食管癌细胞的增殖、侵袭和迁移能力。