The alternative spliced 3'-UTR mediated differential secretion of macrophage colony stimulating factor in breast cancer cells

Biochem Biophys Res Commun. 2020 May 14;525(4):1004-1010. doi: 10.1016/j.bbrc.2020.03.007. Epub 2020 Mar 13.

Abstract

CSF-1 mRNA 3'UTR variants (var) are generated from alternative splicing. CSF-1 protein encoded by var-1 mRNA with long 3'UTR derived from exon-10 is rapidly secreted compared to the CSF-1 protein encoded by var-4 mRNA with short 3'UTR derived from exon-9. Secretion kinetics indicates that HuR, which binds the CSF-1 var-1 mRNA, but not var-4 mRNA, accelerates the secretion of CSF-1 protein. HuR overexpression increases the secretion rate of CSF-1 protein. In contrast, silencing of HuR does not have such an effect, suggesting other compensatory mechanisms. Effect of the CSF-1 mRNA variant 3'UTRs on cellular phenotype shows both CSF-1 var-1 or -4 mRNA is involved in the enhanced rates of migration and invasion observed by both in vitro in breast cancer cells. Our study indicates that the alternative splicing of CSF-1 mRNA 3'UTR can regulate differential secretion of CSF-1 protein.

Keywords: CSF-1 differential secretion; HuR; Var-1 long 3′UTR; Var-4 short 3′UTR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions*
  • Alternative Splicing
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Cell Line, Tumor
  • Cell Movement / genetics
  • ELAV-Like Protein 1 / genetics
  • ELAV-Like Protein 1 / metabolism*
  • Female
  • Gene Silencing
  • Humans
  • Macrophage Colony-Stimulating Factor / genetics
  • Macrophage Colony-Stimulating Factor / metabolism*

Substances

  • 3' Untranslated Regions
  • CSF1 protein, human
  • ELAV-Like Protein 1
  • ELAVL1 protein, human
  • Macrophage Colony-Stimulating Factor