Molecular interactions of miR-338 during tumor progression and metastasis

Cell Mol Biol Lett. 2021 Apr 7;26(1):13. doi: 10.1186/s11658-021-00257-w.

Abstract

Background: Cancer, as one of the main causes of human deaths, is currently a significant global health challenge. Since the majority of cancer-related deaths are associated with late diagnosis, it is necessary to develop minimally invasive early detection markers to manage and reduce mortality rates. MicroRNAs (miRNAs), as highly conserved non-coding RNAs, target the specific mRNAs which are involved in regulation of various fundamental cellular processes such as cell proliferation, death, and signaling pathways. MiRNAs can also be regulated by long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs). They are highly stable in body fluids and have tumor-specific expression profiles, which suggest their suitability as efficient non-invasive diagnostic and prognostic tumor markers. Aberrant expression of miR-338 has been widely reported in different cancers. It regulates cell proliferation, migration, angiogenesis, and apoptosis in tumor cells.

Main body: In the present review, we have summarized all miR-338 interactions with other non-coding RNAs (ncRNAs) and associated signaling pathways to clarify the role of miR-338 during tumor progression.

Conclusions: It was concluded that miR-338 mainly functions as a tumor suppressor in different cancers. There were also significant associations between miR-338 and other ncRNAs in tumor cells. Moreover, miR-338 has a pivotal role during tumor progression using the regulation of WNT, MAPK, and PI3K/AKT signaling pathways. This review highlights miR-338 as a pivotal ncRNA in biology of tumor cells.

Keywords: Biomarker; Cancer; MiR-338; MicroRNA; Non-coding RNA.

Publication types

  • Review

MeSH terms

  • Disease Progression
  • Humans
  • MicroRNAs / metabolism*
  • Mitogen-Activated Protein Kinases / metabolism
  • Neoplasm Metastasis
  • Neoplasms / genetics
  • Neoplasms / pathology*
  • Phosphatidylinositol 3-Kinases / metabolism
  • RNA, Circular / metabolism
  • RNA, Long Noncoding / metabolism
  • Signal Transduction / genetics

Substances

  • MIRN338 microRNA, human
  • MicroRNAs
  • RNA, Circular
  • RNA, Long Noncoding
  • Mitogen-Activated Protein Kinases