Du Jin, Zhao Yang, Hu Dinghui, Li Hang, Gao Lei, Liu Zuntao, Shi Kaihu
Department of Cardiothoracic Surgery, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210028, P.R. China.
Jiangsu Province Academy of Traditional Chinese Medicine, Nanjing, Jiangsu 210028, P.R. China.
Oncol Lett. 2022 Jun 20;24(2):271. doi: 10.3892/ol.2022.13391. eCollection 2022 Aug.
Esophageal squamous cell carcinoma (ESCC) is a deadly disease that seriously affects global public health. The aim of the present study was to explore the role of integrin subunit α3 (ITGA3) in ESCC and investigate its detailed molecular mechanisms. Using reverse transcription-quantitative PCR (RT-qPCR) and western blotting, the mRNA and protein expression of ITGA3 in cell lines was detected. In addition, a series of cellular biological experiments, including Cell Counting Kit-8, wound-healing, Transwell and TUNEL assays, were used to evaluate proliferation, migration, invasion and apoptosis, respectively. Furthermore, western blotting was used to measure the expression of corresponding proteins. ITGA3 was found to be upregulated in ESCC cell lines (ECA109 and TE1). It was also found that ITGA3 silencing inhibited the proliferation, migration, invasion and autophagy of ECA109 and TE1 cells but promoted their apoptosis. In addition, ITGA3 silencing was found to inhibit the FAK/PI3K/AKT signaling pathway. In conclusion, ITGA3 knockdown suppressed cell proliferation, invasion, migration and autophagy in ECA109 and TE1 cells, suggesting that ITGA3 may be a potential therapeutic target for the treatment of ESCC.
食管鳞状细胞癌(ESCC)是一种严重影响全球公众健康的致命疾病。本研究的目的是探讨整合素亚基α3(ITGA3)在ESCC中的作用,并研究其详细的分子机制。采用逆转录定量聚合酶链反应(RT-qPCR)和蛋白质免疫印迹法检测细胞系中ITGA3的mRNA和蛋白质表达。此外,还进行了一系列细胞生物学实验,包括细胞计数试剂盒-8法、伤口愈合实验、Transwell实验和TUNEL实验,分别用于评估细胞的增殖、迁移、侵袭和凋亡。此外,蛋白质免疫印迹法用于检测相应蛋白质的表达。结果发现,ESCC细胞系(ECA109和TE1)中ITGA3表达上调。还发现,ITGA3沉默可抑制ECA109和TE1细胞的增殖、迁移、侵袭和自噬,但促进其凋亡。此外,发现ITGA3沉默可抑制FAK/PI3K/AKT信号通路。总之,ITGA3基因敲低抑制了ECA109和TE1细胞的增殖、侵袭、迁移和自噬,提示ITGA3可能是治疗ESCC的潜在治疗靶点。