首页> 外文期刊>Molecular Carcinogenesis >MiR-107 down-regulates SIAH1 expression in human breast cancer cells and silencing of miR-107 inhibits tumor growth in a nude mouse model of triple-negative breast cancer
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MiR-107 down-regulates SIAH1 expression in human breast cancer cells and silencing of miR-107 inhibits tumor growth in a nude mouse model of triple-negative breast cancer

机译:MiR-107下调人乳腺癌细胞中SIAH1的表达,而miR-107沉默可抑制三阴性乳腺癌的裸鼠模型中的肿瘤生长

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We have reported that SIAH1 is down-regulated and associated with apoptosis and invasion in human breast cancer. However, the molecular mechanisms leading to SIAH1 down-regulation remain to be elucidated. Here, we demonstrated that miR-107 directly down-regulates SIAH1 expression in human breast cancer cells. Over- expression of miR-107 reduced SIAH1 expression, promoted human breast cancer cell proliferation, colony formation, migration and invasion, and inhibited apoptosis. On the contrary, silencing of miR-107 increased SIAH1 expression and inhibited the tumor growth of MDA-MB-231 cells, a kind of triple-negative breast cancer (TNBC) cells, in vitro and in vivo. Our results reveal that miR-107 is an upstream regulator for SIAH1 down-regulation in human breast cancer cells and miR-107 provides a potential effective target for the treatment of TNBC. (c) 2015 Wiley Periodicals, Inc.
机译:我们已经报道SIAH1被下调,并与人类乳腺癌中的细胞凋亡和侵袭有关。然而,导致SIAH1下调的分子机制仍有待阐明。在这里,我们证明了miR-107直接下调人乳腺癌细胞中SIAH1的表达。 miR-107的过表达降低了SIAH1的表达,促进了人类乳腺癌细胞的增殖,集落形成,迁移和侵袭,并抑制了细胞凋亡。相反,miR-107沉默后在体内和体外增加了SIAH1表达并抑制了MDA-MB-231细胞(一种三阴性乳腺癌(TNBC)细胞)的肿瘤生长。我们的结果显示,miR-107是人乳腺癌细胞中SIAH1下调的上游调节剂,而miR-107为TNBC的治疗提供了潜在的有效靶点。 (c)2015年威利期刊有限公司

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