AI Article Synopsis

  • MicroRNAs, specifically miR-605, are implicated in the development and progression of melanoma, with its downregulation observed in both melanoma cell lines and clinical samples.
  • Functional studies show that miR-605 inhibits melanoma cell growth by targeting the INPP4B gene, which is linked to SGK3 activation.
  • These findings suggest that miR-605 acts as a tumor suppressor in melanoma and could be a promising target for future cancer therapies.

Article Abstract

MicroRNAs (miRNAs) play crucial roles in the initiation and progression of various cancers, including melanoma. Recently, the genetic variants and deregulation of miR-605 have been reported to participate in carcinogenesis. However, the expression status of the miR-605 in melanoma tissues and its role in melanoma progression remain unknown. In this study, we found that miR-605 was significantly downregulated in melanoma cell lines and clinical specimens. Further function studies demonstrated that miR-605 suppressed melanoma cell growth both in vitro and in vivo. Moreover, INPP4B gene was identified as a target of miR-605 through bioinformatics analysis and luciferase reporter assays. Further analysis demonstrated that the inhibition of INPP4B mediated SGK3 activation was required for the suppressive role of miR-605 on melanomas cell growth. Collectively, our data suggest that miR-605 functions as a tumor suppressor by negatively regulating INPP4B mediated SGK3 activation in melanoma and may present a potential target for therapeutic intervention.

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http://dx.doi.org/10.3892/or.2017.5740DOI Listing

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