NEAT1是乳腺癌细胞通过FUS和miR-548存活所必需的。

Gene regulation and systems biology Pub Date : 2016-04-27 eCollection Date: 2016-01-01 DOI:10.4137/GRSB.S29414
Hao Ke, Limin Zhao, Xu Feng, Haibo Xu, Li Zou, Qin Yang, Xiaosan Su, Lingtao Peng, Baowei Jiao
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引用次数: 124

摘要

越来越多的证据表明,长链非编码rna (lncRNAs)在调节多种细胞过程中发挥重要作用,包括细胞分裂、细胞生长和凋亡,以及癌症转移和神经系统疾病的进展;然而,lncrna调控这些过程的机制尚不清楚。在本研究中,我们发现下调lncRNA核旁斑组装转录本1 (NEAT1)在乳腺癌细胞中的表达可抑制细胞生长并诱导细胞凋亡。此外,肉瘤中融合的rna结合蛋白/脂肉瘤易位蛋白(FUS/TLS)与NEAT1发生物理相互作用,降低FUS/TLS的表达也会诱导细胞凋亡。多种mirna被鉴定为NEAT1的调节因子,但只有过表达miR-548ar才能降低NEAT1的表达并促进细胞凋亡。这些结果表明NEAT1、miR-548ar-3p和FUS之间存在一种新的相互作用,以及它们在调节乳腺癌细胞凋亡中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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NEAT1 is Required for Survival of Breast Cancer Cells Through FUS and miR-548.

Increasing evidence shows that long noncoding RNAs (lncRNAs) have important roles in the regulation of multiple cellular processes, including cell division, cell growth, and apoptosis, as well as cancer metastasis and neurological disease progression; however, the mechanism of how lncRNAs regulate these processes is not well established. In this study, we demonstrated that downregulating the expression of the lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) in breast cancer cells inhibited cell growth and induced cell apoptosis. In addition, the RNA-binding protein fused in sarcoma/translocated in liposarcoma (FUS/TLS) physically interacted with NEAT1, and reducing the expression of FUS/TLS also induced cell apoptosis. Multiple miRNAs were identified as regulators of NEAT1, but only overexpression of miR-548ar was able to decrease NEAT1 expression and promote apoptosis. These results indicate a novel interaction between NEAT1, miR-548ar-3p, and FUS and their role in the regulation of breast cancer cell apoptosis.

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