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微小RNA-142-5p通过靶向磷脂酰肌醇-4,5-二磷酸3-激酶催化亚基α抑制非小细胞肺癌的肿瘤发生

MiR-142-5p Suppresses Tumorigenesis by Targeting PIK3CA in Non-Small Cell Lung Cancer.

作者信息

Wang Zhao, Liu Zhimin, Fang Xiaojie, Yang Han

机构信息

Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, China.

Department of Gastric and Pancreatic Surgery, Sun Yat-sen University Cancer Center, Guangzhou, China.

出版信息

Cell Physiol Biochem. 2017;43(6):2505-2515. doi: 10.1159/000484459. Epub 2017 Oct 31.

Abstract

BACKGROUND/AIMS: Numerous studies have demonstrated that aberrant microRNA (miRNA) expression is involved in human disease including cancer. To date, the potential miRNAs regulating lung cancer growth and progression are not fully identified yet.

METHODS

In this study, the expression of miR-142-5p was measured in non-small cell lung cancer tissue and cell lines by qRT-PCR. The functional assays including the cell viability, colony formation, cell migration and invasion were performed in miR-142-5p mimic or inhibitor transfected cell lines (in vitro) and the cell tumorigenesis in nude mice (in vivo). The fluorescence ratios of cell viability were recorded using a multi-plate reader (Synergy 2, BioTek, Winooski, VT, USA) and the colonies were counted using an ELIspot Bioreader 5000 (BIO-SYS, Karben, GE).

RESULTS

MiR-142-5p was significantly downregulated in non-small cell lung cancer tissue and cell lines compared to normal human lung tissues. Overexpression of miR-142-5p resulted in decreased expression of PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha) at both mRNA and protein levels. We found that miR-142-5p overexpression markedly suppressed cell proliferation in vitro and in vivo. Conversely, inhibition of miR-142-5p promoted lung cancer growth. Mechanistic studies showed that PIK3CA was a potential target of miR-142-5p and it mediated reduction of PIK3CA resulting in suppression of PI3K/Akt pathway.

CONCLUSIONS

Our results demonstrate that miR-142-5p functions as a growth suppressive miRNA and plays an important role in inhibiting the tumorigenesis through targeting PIK3CA in non-small cell lung cancer.

摘要

背景/目的:大量研究表明,异常的微小RNA(miRNA)表达与包括癌症在内的人类疾病有关。迄今为止,调节肺癌生长和进展的潜在miRNA尚未完全确定。

方法

在本研究中,通过qRT-PCR检测非小细胞肺癌组织和细胞系中miR-142-5p的表达。在转染了miR-142-5p模拟物或抑制剂的细胞系中进行包括细胞活力、集落形成、细胞迁移和侵袭在内的功能测定(体外)以及在裸鼠中进行细胞肿瘤发生实验(体内)。使用多功能酶标仪(Synergy 2,BioTek,美国佛蒙特州威努斯基)记录细胞活力的荧光比率,并使用ELIspot Bioreader 5000(BIO-SYS,德国卡本)计数集落。

结果

与正常人类肺组织相比,miR-142-5p在非小细胞肺癌组织和细胞系中显著下调。miR-142-5p的过表达导致PIK3CA(磷脂酰肌醇-4,5-二磷酸3-激酶,催化亚基α)在mRNA和蛋白质水平上的表达降低。我们发现miR-142-5p的过表达在体外和体内均显著抑制细胞增殖。相反,抑制miR-142-5p促进肺癌生长。机制研究表明,PIK3CA是miR-142-5p的潜在靶点,它介导了PIK3CA的减少,从而导致PI3K/Akt信号通路的抑制。

结论

我们的结果表明,miR-142-5p作为一种生长抑制性miRNA发挥作用,并通过靶向PIK3CA在非小细胞肺癌中抑制肿瘤发生起重要作用。

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