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miR-3178 inhibits cell proliferation and metastasis by targeting Notch1 in triple-negative breast cancer

机译:miR-3178通过靶向三阴性乳腺癌中的Notch1抑制细胞增殖和转移

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Triple-negative breast cancer (TNBC) has a poorer outcome than other subtypes of breast cancer, and the discovery of dysregulated microRNA (miRNA) and their role in tumor progression has provided a new avenue for elucidating the mechanism involved in TNBC. In this study, we identified that miR-3178 was significantly reduced in TNBC, and the low miR-3178 expression correlated with poor overall survival in TNBC but not in non-TNBC. The ectopic overexpression of miR-3178 suppressed TNBC cell proliferation, invasion, and migration by inhibiting the epithelial-to-mesenchymal (EMT) transition. Notch1 was validated as the direct target gene of miR-3178, which was confirmed by the dual-luciferase reporter assay. miR-3178 decreased the expression of Notch1 and restoration of Notch1 expression attenuated the inhibitory effects of miR-3178 on cell proliferation, metastasis, and the EMT in TNBC. miR-3178 inhibited cell proliferation and metastasis by targeting Notch1 in TNBC, and the restoration of miR-3178 might be a potential therapeutic strategy for TNBC.
机译:三阴性乳腺癌(TNBC)的结果要比其他亚型的乳腺癌差,而microRNA(miRNA)失调及其在肿瘤进展中的作用的发现为阐明TNBC涉及的机制提供了新途径。在这项研究中,我们发现TNBC中miR-3178显着降低,而miR-3178的低表达与TNBC中较差的总体存活率相关,而与非TNBC无关。 miR-3178的异位过表达通过抑制上皮到间充质(EMT)的过渡来抑制TNBC细胞的增殖,侵袭和迁移。 Notch1被证实是miR-3178的直接靶基因,这已通过双荧光素酶报告基因检测法得以证实。 miR-3178降低了Notch1的表达,Notch1表达的恢复减弱了miR-3178对TNBC中细胞增殖,转移和EMT的抑制作用。 miR-3178通过靶向TNBC中的Notch1抑制细胞增殖和转移,而miR-3178的恢复可能是TNBC的潜在治疗策略。

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