Entity of In Vitro Toxicology and Dermato-Cosmetology, Department of Pharmaceutical and Pharmacological Sciences, Vrije Universiteit Brussel, Laarbeeklaan 103, 1090 Brussels, Belgium.
Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, Av. Prof. Dr. Orlando Marques de Paiva 87, Cidade Universitária, São Paulo 05508-270, Brazil.
Int J Mol Sci. 2021 Nov 10;22(22):12187. doi: 10.3390/ijms222212187.
Liver cancer cell lines are frequently used in vitro tools to test candidate anti-cancer agents as well as to elucidate mechanisms of liver carcinogenesis. Among such mechanisms is cellular communication mediated by connexin-based gap junctions. The present study investigated changes in connexin expression and gap junction functionality in liver cancer in vitro. For this purpose, seven human liver cancer cell lines, as well as primary human hepatocytes, were subjected to connexin and gap junction analysis at the transcriptional, translational and activity level. Real-time quantitative reverse transcription polymerase chain reaction analysis showed enhanced expression of connexin43 in the majority of liver cancer cell lines at the expense of connexin32 and connexin26. Some of these changes were paralleled at the protein level, as evidenced by immunoblot analysis and in situ immunocytochemistry. Gap junctional intercellular communication, assessed by the scrape loading/dye transfer assay, was generally low in all liver cancer cell lines. Collectively, these results provide a full scenario of modifications in hepatocyte connexin production and gap junction activity in cultured liver cancer cell lines. The findings may be valuable for the selection of neoplastic hepatocytes for future mechanistic investigation and testing of anti-cancer drugs that target connexins and their channels.
肝癌细胞系常用于体外工具,以测试候选抗癌药物,并阐明肝癌发生的机制。在这些机制中,细胞通讯是由连接蛋白形成的缝隙连接介导的。本研究调查了肝癌中连接蛋白表达和缝隙连接功能的变化。为此,本研究在转录、翻译和活性水平上对 7 个人肝癌细胞系以及原代人肝细胞进行了连接蛋白和缝隙连接分析。实时定量逆转录聚合酶链反应分析显示,大多数肝癌细胞系中连接蛋白 43 的表达增强,而连接蛋白 32 和连接蛋白 26 的表达减少。一些变化在蛋白质水平上得到了印证,免疫印迹分析和原位免疫细胞化学证实了这一点。划痕加载/染料转移试验评估的缝隙连接细胞间通讯在所有肝癌细胞系中通常都较低。总的来说,这些结果提供了肝癌细胞系中肝细胞连接蛋白产生和缝隙连接活性改变的完整情况。这些发现对于选择用于未来机制研究和测试以连接蛋白及其通道为靶点的抗癌药物的肿瘤性肝细胞可能具有重要价值。