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MicroRNA-34a suppresses the breast cancer stem cell-like characteristics by downregulating Notch1 pathway

机译:MicroRNA-34a通过下调Notch1途径抑制乳腺癌干细胞样特征

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摘要

MicroRNAs play pivotal roles in cancer stem cell regulation. Previous studies have shown that microRNA-34a (miR-34a) is downregulated in human breast cancer. However, it is unknown whether and how miR-34a regulates breast cancer stem cells. Notch signaling is one of the most important pathways in stem cell maintenance and function. In this study, we verified that miR-34a directly and functionally targeted Notch1 in MCF-7 cells. We reported that miR-34a negatively regulated cell proliferation, migration, and invasion and breast cancer stem cell propagation by downregulating Notch1. The expression of miR-34a was negatively correlated with tumor stages, metastasis, and Notch1 expression in breast cancer tissues. Furthermore, overexpression of miR-34a increased chemosensitivity of breast cancer cells to paclitaxel (PTX) by downregulating the Notch1 pathway. Mammosphere formation and expression of the stemness factor ALDH1 were also reduced in the cells treated with miR-34a and PTX compared to those treated with PTX alone. Taken together, our results indicate that miR-34a inhibited breast cancer stemness and increased the chemosensitivity to PTX partially by downregulating the Notch1 pathway, suggesting that miR-34a/Notch1 play an important role in regulating breast cancer stem cells. Thus miR-34a is a potential target for prevention and therapy of breast cancer.
机译:MicroRNA在癌症干细胞调节中起关键作用。先前的研究表明,microRNA-34a(miR-34a)在人类乳腺癌中被下调。但是,尚不清楚miR-34a是否以及如何调节乳腺癌干细胞。 Notch信号传导是干细胞维持和功能中最重要的途径之一。在这项研究中,我们验证了miR-34a直接和功能靶向MCF-7细胞中的Notch1。我们报道,miR-34a通过下调Notch1负调控细胞增殖,迁移和侵袭以及乳腺癌干细胞的增殖。 miR-34a的表达与乳腺癌组织中的肿瘤分期,转移和Notch1表达呈负相关。此外,miR-34a的过表达通过下调Notch1途径提高了乳腺癌细胞对紫杉醇(PTX)的化学敏感性。与单独用PTX处理的​​细胞相比,用miR-34a和PTX处理的​​细胞的乳球形成和干因子ALDH1的表达也减少了。两者合计,我们的结果表明,miR-34a通过下调Notch1途径部分抑制乳腺癌干细胞并提高对PTX的化学敏感性,这表明miR-34a / Notch1在调节乳腺癌干细胞中起重要作用。因此,miR-34a是预防和治疗乳腺癌的潜在靶标。

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