Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1931254 | Biochemical and Biophysical Research Communications | 2011 | 7 Pages |
MicroRNAs (miRNAs) are epigenetic regulators of gene expression, and their deregulation plays an important role in human cancer, including oral squamous cell carcinoma (OSCC). Recently, we found that miRNA-181a (miR-181a) was upregulated during replicative senescence of normal human oral keratinocytes. Since senescence is considered as a tumor suppressive mechanism, we thus investigated the expression and biological role of miR-181a in OSCC. We found that miR-181a was frequently downregulated in OSCC. Ectopic expression of miR-181a suppressed proliferation and anchorage independent growth ability of OSCC. Moreover, miR-181a dramatically reduces the growth of OSCC on three dimensional organotypic raft culture. We also identified K-ras as a novel target of miR-181a. miR-181a decreased K-ras protein level as well as the luciferase activity of reporter vectors containing the 3′-untranslated region of K-ras gene. Finally, we defined a minimal regulatory region of miR-181a and found a positive correlation between its promoter activity and the level of miR-181a expression. In conclusion, miR-181a may function as an OSCC suppressor by targeting on K-ras oncogene. Thus, miR-181a should be considered for therapeutic application for OSCC.
Research highlights► MicroRNA-181a (miR-181a) was frequently downregulated in oral squamous cell carcinoma (OSCC). ► Overexpression of miR-181a suppressed OSCC growth. ► K-ras is a novel target of miR-181a. ► Decreased miR-181a expression is attributed to its lower promoter activity in OSCC.