Department of Pediatric Surgery, The Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong, China.
FEBS Lett. 2013 Nov 15;587(22):3729-37. doi: 10.1016/j.febslet.2013.09.044. Epub 2013 Oct 15.
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.
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。