首页> 外文期刊>Molecular medicine reports >MicroRNA-133a inhibits proliferation and invasion, and induces apoptosis in gastric carcinoma cells via targeting fascin actin-bundling protein 1
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MicroRNA-133a inhibits proliferation and invasion, and induces apoptosis in gastric carcinoma cells via targeting fascin actin-bundling protein 1

机译:MicroRNA-133A抑制增殖和侵袭,并通过靶向诱导菌肌蛋白捆绑蛋白1诱导胃癌细胞凋亡

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摘要

Fascin actin-bundling protein 1 (FSCN1) is associated with tumor progression. In addition, deregulation of the expression of FSCN1 has been observed in certain types of cancer. However, the detailed role of FSCN1 in gastric cancer remains to be elucidated. In the present study, downregulation of microRNA (miR)-133a and upregulation of FSCN1 were both observed in gastric cancer tissues and cell lines. Functional studies have revealed that miR-133a is able to bind to the 3-untranslated region of FSCN1 mRNA, and overexpression of miR-133a causes downregulation of FSCN1 expression, while downregulation of miR-133a leads to an increased FSCN1 expression in gastric cancer cells. Furthermore, overexpression of miR-133a inhibited proliferation and invasion, but promoted apoptosis of gastric cancer cells, which may be reversed by upregulation of FSCN1. By contrast, downregulation of miR-133a enhanced proliferation and invasion, but suppressed apoptosis in gastric cancer cells. In conclusion, the anti-oncogenic activity of miR-133a may involve the inhibition of the target gene FSCN1. The present study suggested that miR-133a may be a potential therapeutic target in the treatment of gastric cancer.
机译:肌动蛋白集束蛋白1(FSCN1)与肿瘤进展相关。此外,FSCN1的表达的失调已经在某些类型的癌症观察到。然而,FSCN1在胃癌遗体癌症的具体作用,待澄清。在本研究中,微RNA(MIR)-133a和FSCN1的上调的下调是在胃癌组织和细胞系中观察到二者。功能的研究已经揭示了miR-133a的是能够结合FSCN1 mRNA的3非翻译区,和miR-133a的过表达导致FSCN1表达的下调,而的miR-133a的引线到的下调在胃癌细胞中增加的FSCN1表达。此外,的miR-133a的表达抑制增殖和侵袭,但胃癌细胞,其可通过FSCN1的上调被颠倒的促进细胞凋亡。与此相反,在胃癌细胞中的miR-133a的增强的增殖和侵袭,但抑制细胞凋亡的下调。最后,的miR-133a的抗致癌活性可涉及靶基因FSCN1的抑制。本研究提示了miR-133a的可在胃癌的治疗的潜在治疗靶标。

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