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miR-96 通过上皮间质转化调控转化生长因子-β1 诱导的膀胱癌迁移和侵袭

miR-96 regulates migration and invasion of bladder cancer through epithelial-mesenchymal transition in response to transforming growth factor-β1.

机构信息

Putuo Hospital, Shanghai University of Traditional Chinese Medicine, China.

出版信息

J Cell Biochem. 2018 Sep;119(9):7807-7817. doi: 10.1002/jcb.27172. Epub 2018 Jun 19.

Abstract

Bladder cancer (BC) is one of the most frequent urological malignancies, and its molecular mechanism still remains unclear. Recent studies have revealed that MicroRNA (miRNAs) acted as oncogenes or tumor suppressors in a variety of cancers. MiRNA-96 has been reported to play a significant role in the development and progression of many cancers. In the current study, we found that transforming growth factor (TGF)-β1 played a significant role in the progression that miR-96 conducted. And TGF-β1 could also regulate the expression of FOXQ1, which is the target gene of miR-96. Furthermore, miR-96 induced epithelial-mesenchymal transition in BC cells, which is driven by TGF-β1. In conclusion, our data revealed that miR-96 regulates the progression and epithelial-mesenchymal transition, which is driven by TGF-β1 in BC cells; it may provide a new thought for the therapy of BC.

摘要

膀胱癌(BC)是最常见的泌尿系统恶性肿瘤之一,其分子机制尚不清楚。最近的研究表明,MicroRNA(miRNA)在多种癌症中作为癌基因或肿瘤抑制因子发挥作用。miRNA-96 已被报道在许多癌症的发展和进展中发挥重要作用。在本研究中,我们发现转化生长因子(TGF)-β1 在 miR-96 介导的进展中起重要作用。而且 TGF-β1 还可以调节 miR-96 的靶基因 FOXQ1 的表达。此外,miR-96 诱导 TGF-β1 驱动的 BC 细胞上皮-间充质转化。总之,我们的数据表明,miR-96 通过 TGF-β1 调节 BC 细胞的进展和上皮-间充质转化,可能为 BC 的治疗提供新的思路。

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