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miR-338-3p 通过靶向 PREX2a 抑制神经母细胞瘤的增殖、侵袭和迁移。

miR-338-3p suppresses neuroblastoma proliferation, invasion and migration through targeting PREX2a.

机构信息

Department of Pediatric Surgery, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong, China.

出版信息

FEBS Lett. 2013 Nov 15;587(22):3729-37. doi: 10.1016/j.febslet.2013.09.044. Epub 2013 Oct 15.

Abstract

MicroRNAs (miRNA) can regulate cancer cell proliferation and metastasis. Here, we show that miR-338-3p is down-regulated in metastatic tumor tissues compared to primary tumors, and that that miR-338-3p can inhibit cell proliferation by inducing cell cycle arrest, as well as restrain cell migration and invasion. PREX2a is confirmed as a direct target of miR-338-3p. Knockdown of PREX2a inhibits cell proliferation, migration and invasion through the PTEN/Akt pathway. miR-338-3p-dependent inhibition of proliferation and invasion can be rescued by PREXa. Overall, this study demonstrates that miR-338-3p affects the PTEN/Akt pathway by down-regulating PREX2a. This newly identified function of miR-338-3p provides novel insights into neuroblastoma and may foster therapeutic applications.

摘要

微小 RNA(miRNA)可调节癌细胞的增殖和转移。在这里,我们发现与原发性肿瘤相比,转移性肿瘤组织中 miR-338-3p 下调,miR-338-3p 通过诱导细胞周期停滞,以及抑制细胞迁移和侵袭,从而抑制细胞增殖。PREX2a 被确认为 miR-338-3p 的直接靶标。通过 PTEN/Akt 通路,PREX2a 的敲低抑制细胞增殖、迁移和侵袭。通过 PREXa 可挽救 miR-338-3p 依赖性的增殖和侵袭抑制。总的来说,本研究表明 miR-338-3p 通过下调 PREX2a 影响 PTEN/Akt 通路。miR-338-3p 的这一新功能为神经母细胞瘤提供了新的见解,并可能促进治疗应用。

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