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MiR-485-3p and miR-485-5p suppress breast cancer cell metastasis by inhibiting PGC-1α expression

机译:MiR-485-3P和MIR-485-5P通过抑制PGC-1 α表达来抑制乳腺癌细胞转移

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Breast cancer is the worldwide leading cause of cancer mortality in women. The majority of deaths from breast cancer arise from metastasis of local tumors. Cancer cells support their rapid proliferation by diverting metabolites into anabolic pathways, but during cancer metastasis, the proliferative program of invasive cancer cells is suspended for a migratory phenotype. In this study, we demonstrated that both mature forms of miRNA-485, miR-485-3p and miR-485-5p were involved in regulating mitochondrial respiration, cell migration and cell invasion in breast cancer cells by directly targeting and inhibiting the expression of PGC-1 α . Specifically, the expression levels of both miR-485-3p and miR-485-5p were decreased in breast cancer tissues. Overexpression of miR-485-3p and miR-485-5p suppressed mitochondrial respiration and potential for cell migration and invasion in vitro , and also inhibited spontaneous metastasis of breast cancer cells in vivo . The suppression of mitochondrial respiration and cell invasion could be partially relieved by restoration of PGC-1 α expression.
机译:乳腺癌是妇女癌症死亡率的全球主要原因。来自乳腺癌的大多数死亡来自局部肿瘤的转移。癌细胞通过将代谢物转移到代谢途径中,支持它们的快速增殖,但在癌症转移期间,侵入性癌细胞的增殖程序暂停迁移表型。在这项研究中,我们证明,通过直接靶向和抑制表达,涉及调节乳腺癌细胞的线粒体呼吸,细胞迁移和细胞侵袭,涉及调节线粒体呼吸,细胞迁移和细胞侵袭的成熟形式PGC-1α。具体地,MIR-485-3P和MIR-485-5P的表达水平在乳腺癌组织中降低。 miR-485-3p和miR-485-5p的过表达抑制了体外细胞迁移和侵袭的线粒体呼吸和潜力,并且还抑制了体内乳腺癌细胞的自发转移。通过恢复PGC-1α表达,可以部分缓解线粒体呼吸和细胞侵袭。

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