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Long non-coding RNA PICSAR decreases adhesion and promotes migration of squamous carcinoma cells by downregulating α2β1 and α5β1 integrin expression

机译:长的非编码RNA PICSAR通过下调α2β1和α5β1整联蛋白的表达来降低黏附并促进鳞状癌细胞的迁移

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Long non-coding RNAs (lncRNAs) regulate various cellular processes, and they have emerged as potential biomarkers and therapeutic targets in cancer. We have previously characterized the oncogenic role of lncRNA PICSAR (p38 inhibited cutaneous squamous cell carcinoma associated lincRNA) in cutaneous squamous cell carcinoma (cSCC), the most common metastatic skin cancer. In this study, we show that knockdown of PICSAR in cSCC cells upregulates expression of α2, α5 and β1 integrins, resulting in increased cell adhesion and decreased cell migration on collagen I and fibronectin. In contrast, overexpression of PICSAR in cSCC cells downregulates expression of α2, α5 and β1 integrins on cell surface, resulting in decreased cell adhesion on collagen I and fibronectin and increased cell migration. These results demonstrate a novel mechanism for regulation of the expression of collagen and fibronectin binding integrins by lncRNA PICSAR, leading to altered adhesion and migration of cSCC cells.This article has an associated First Person interview with the first author of the paper.
机译:长的非编码RNA(lncRNA)调节各种细胞过程,它们已成为潜在的生物标志物和癌症的治疗靶标。我们先前已经表征了lncRNA PICSAR(p38抑制与皮肤鳞状细胞癌相关的lincRNA的致癌作用)在皮肤鳞状细胞癌(cSCC)(最常见的转移性皮肤癌)中的作用。在这项研究中,我们表明在cSCC细胞中PICSAR的敲低会上调α2,α5和β1整联蛋白的表达,从而导致细胞黏附增加并减少胶原蛋白I和纤连蛋白上的细胞迁移。相反,PICSAR在cSCC细胞中的过表达下调了细胞表面上α2,α5和β1整联蛋白的表达,从而导致胶原蛋白和纤连蛋白上的细胞粘附减少,并增加了细胞迁移。这些结果证明了通过lncRNA PICSAR调节胶原蛋白和纤连蛋白结合整联蛋白表达的新机制,从而导致cSCC细胞的粘附和迁移发生了变化。本文与第一人相关的第一人称采访。

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