Exosome-Derived miR-25-3p and miR-92a-3p Stimulate Liposarcoma Progression

Cancer Res. 2017 Jul 15;77(14):3846-3856. doi: 10.1158/0008-5472.CAN-16-2984. Epub 2017 Jun 6.

Abstract

Despite the development of combined modality treatments against liposarcoma in recent years, a significant proportion of patients respond only modestly to such approaches, possibly contributing to local or distant recurrence. Early detection of recurrent or metastatic disease could improve patient prognosis by triggering earlier clinical intervention. However, useful biomarkers for such purposes are lacking. Using both patient plasma samples and cell lines, we demonstrate here that miR-25-3p and miR-92a-3p are secreted by liposarcoma cells through extracellular vesicles and may be useful as potential biomarkers of disease. Both miR-25-3p and miR-92a-3p stimulated secretion of proinflammatory cytokine IL6 from tumor-associated macrophages in a TLR7/8-dependent manner, which in turn promoted liposarcoma cell proliferation, invasion, and metastasis via this interaction with the surrounding microenvironment. Our findings provide novel and previously unreported insight into liposarcoma progression, identifying communication between liposarcoma cells and their microenvironment as a process critically involved in liposarcoma progression. This study establishes the possibility that the pattern of circulating miRNAs may identify recurrence prior to radiological detectability while providing insight into disease outcome and as a possible approach to monitor treatment efficacy. Cancer Res; 77(14); 3846-56. ©2017 AACR.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Case-Control Studies
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Disease Progression
  • Exosomes / metabolism*
  • HEK293 Cells
  • Humans
  • Liposarcoma / blood
  • Liposarcoma / genetics*
  • Liposarcoma / pathology
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / metabolism*
  • Transfection

Substances

  • MIRN25 microRNA, human
  • MIRN25 microRNA, mouse
  • MIRN92 microRNA, human
  • MicroRNAs
  • Mirn92 microRNA, mouse