Suppr超能文献

MicroRNA-449a 通过表观遗传调控 ATDC 表达,在胰腺癌中发挥肿瘤抑制作用。

MicroRNA-449a functions as a tumor suppressor in pancreatic cancer by the epigenetic regulation of ATDC expression.

机构信息

Anesthesiology Department, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi Province, 710061, China.

Radiotherapy Department, Shaanxi Provincial Tumor Hospital, Affiliated Hospital of Medical College of Xi'an Jiaotong university, Xi'an, Shaanxi Province, 710061, China.

出版信息

Biomed Pharmacother. 2018 Jul;103:782-789. doi: 10.1016/j.biopha.2018.04.101. Epub 2018 Apr 24.

Abstract

A growing body of evidence has suggested that microRNAs (miRNAs) play a pivotal role in the development and progression of pancreatic cancer. miRNA-449a (miR-449a) has attracted particular interest due to its critical role in regulating cancer biology in numerous cancer types. However, whether miR-449a is involved in the regulation of pancreatic cancer development and progression remains unknown. In this study, we aimed to investigate the expression pattern and potential biological function of miR-449a in pancreatic cancer. Our results showed that miR-449a levels were significantly down-regulated in pancreatic cancer tissues and cell lines. The overexpression of miR-449a significantly inhibited the proliferation and invasion of pancreatic cancer cells, whereas miR-449a inhibition promoted the proliferation and invasion of pancreatic cancer cells. Bioinformatic analysis predicted that ataxia-telangiectasia group D complementing gene (ATDC) was a potential target gene of miR-449a. The dual-luciferase reporter assay revealed that miR-449a directly binds to the 3'-untranslated region of ATDC. Further analysis demonstrated that miR-449a negatively controls the mRNA and protein expression of ATDC in pancreatic cancer cells. In addition, an inverse correlation between miR-449a and ATDC expression was observed in clinical tissues. Notably, the overexpression of ATDC partially reversed the antitumor effect of miR-449a overexpression, while the silencing of ATDC abrogated the oncogenic effect of miR-449a inhibition in pancreatic cancer cells. In addition, the overexpression of miR-449a inhibited the accumulation of β-catenin and blocked the activation of Wnt signaling by targeting ATDC. Taken together, our study reveals a tumor suppressive role of miR-449a in pancreatic cancer, and demonstrates that the antitumor role of miR-449a is associated with its regulatory effect on ATDC expression. Our study suggests that the miR-449a/ATDC axis may play an important role in the development and progression of pancreatic cancer and may provide potential targets for the development of cancer therapies.

摘要

越来越多的证据表明 microRNAs(miRNAs)在胰腺癌的发生和发展中起着关键作用。miRNA-449a(miR-449a)因其在多种癌症类型中调节癌症生物学的关键作用而引起了特别关注。然而,miR-449a 是否参与调节胰腺癌的发生和发展仍不清楚。在这项研究中,我们旨在研究 miR-449a 在胰腺癌中的表达模式和潜在生物学功能。我们的结果表明,miR-449a 在胰腺癌组织和细胞系中的水平显著下调。miR-449a 的过表达显著抑制了胰腺癌细胞的增殖和侵袭,而 miR-449a 的抑制则促进了胰腺癌细胞的增殖和侵袭。生物信息学分析预测共济失调毛细血管扩张症突变基因 D 互补基因(ATDC)是 miR-449a 的一个潜在靶基因。双荧光素酶报告基因实验显示,miR-449a 直接结合到 ATDC 的 3'-非翻译区。进一步分析表明,miR-449a 在胰腺癌细胞中负调控 ATDC 的 mRNA 和蛋白表达。此外,在临床组织中观察到 miR-449a 与 ATDC 表达之间存在负相关关系。值得注意的是,ATDC 的过表达部分逆转了 miR-449a 过表达的抗肿瘤作用,而 miR-449a 抑制沉默则消除了 miR-449a 抑制在胰腺癌细胞中致癌作用。此外,miR-449a 的过表达抑制了 β-连环蛋白的积累,并通过靶向 ATDC 阻断了 Wnt 信号的激活。总之,我们的研究揭示了 miR-449a 在胰腺癌中的肿瘤抑制作用,并表明 miR-449a 的抗肿瘤作用与其对 ATDC 表达的调节作用有关。我们的研究表明,miR-449a/ATDC 轴可能在胰腺癌的发生和发展中起着重要作用,并为癌症治疗的发展提供了潜在的靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验