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MiR-199a targeting ROCK1 to affect kidney cell proliferation, invasion and apoptosis

机译:靶向ROCK1的MiR-199a影响肾细胞增殖,侵袭和凋亡

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Renal cell carcinoma (RCC) is one of the three most common cancers of urinary tract cancer, accounting for 2–3% of all systemic cancers. Recent studies have found that miR-199a is lowly expressed in RCC, may act as a tumour suppressor gene to induce the occurrence of kidney cancer. In the present study, we investigated the role of miR-199a in the progression and metastasis of RCC. The results showed that miR-199a significantly downregulated in RCC and cell lines. Overexpression of miR-199a in RCC cell lines significantly inhibited cell proliferation, migration and invasion. Furthermore, the qRT-PCR and western blot results showed that miR-199a overexpression significantly downregulated ROCK-1 mRNA and protein levels. ROCK1 was identified as a target of miR-199a, and ectopic expression of miR-199a downregulated ROCK1 by direct binding to its 3′ untranslated region. Together, these findings indicate that miR-199a acts as a tumour suppressor and its downregulation in tumour tissues may contribute to the progression and metastasis of RCC through a mechanism involving ROCK1, suggesting miR-199a as a potential new diagnostic and therapeutic target for the treatment of RCC.
机译:肾细胞癌(RCC)是三种最常见的泌尿道癌,占所有系统性癌症的2-3%。最近的研究发现,miR-199a在RCC中的表达很低,可能作为抑癌基因来诱导肾癌的发生。在本研究中,我们调查了miR-199a在RCC的进展和转移中的作用。结果显示,miR-199a在RCC和细胞系中显着下调。 miR-199a在RCC细胞系中的过表达显着抑制了细胞的增殖,迁移和侵袭。此外,qRT-PCR和western blot结果表明,miR-199a过表达显着下调了ROCK-1 mRNA和蛋白水平。 ROCK1被确定为miR-199a的靶标,并且miR-199a的异位表达通过直接与其3'非翻译区结合而下调ROCK1。总之,这些发现表明,miR-199a充当肿瘤抑制因子,其在肿瘤组织中的下调可能通过涉及ROCK1的机制促进RCC的进展和转移,提示miR-199a作为潜在的新诊断和治疗靶标RCC。

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