MiR-99a exerts anti-metastasis through inhibiting myotubularin-related protein 3 expression in oral cancer

Y. Z. Kuo, Y. H. Tai, H. I. Lo, Y. L. Chen, H. C. Cheng, W. Y. Fang, S. H. Lin, C. L. Yang, S. T. Tsai, L. W. Wu

研究成果: Article同行評審

48 引文 斯高帕斯(Scopus)

摘要

Objective: We aimed at studying the role of the most deregulated miR-99a, identifying its downstream targets, and exploring the clinical potential of miR-99a and its target(s) in oral cancer. Subjects and Methods: Following confirmation of miR-99a deregulation in nine oral lines and 26 pairwise clinical specimens, miR-99a-manipulated oral cancer cells were subjected to cell proliferation, migration, invasion, and in vivo murine metastasis assays. We characterized putative miR-99a target(s) using luciferase reporter assays and genetic manipulation. The inverse relation of miR-99a and its target(s) was examined in clinical specimens using real-time PCR and Western blot analysis. Results: MiR-99a down-regulation was confirmed both in tested oral cancer cell lines and clinical specimens. Ectopic miR-99a expression inhibited oral cancer cell migration and invasion. Anti-miR-99a, silencing miR-99a functions, had the opposite effect. Myotubularin-related protein 3 (MTMR3) with one evolutionarily conserved seed region in the 3′-untranslated region was a novel miR-99a target. Depleting MTMR3 expression significantly reduced cell proliferation, migration, or invasion. There was an inverse expression of miR-99a and MTMR3 protein in oral cancer lines and clinical specimens. Conclusion: miR-99a repressed oral cancer cell migration and invasion partly through decreasing MTMR3 expression. MTMR3 may serve as a therapeutic target for oral cancer treatment.

原文English
頁(從 - 到)e65-e75
期刊Oral Diseases
20
發行號3
DOIs
出版狀態Published - 2014 4月

All Science Journal Classification (ASJC) codes

  • 耳鼻咽喉科
  • 一般牙醫學

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