Stromal-dependent tumor promotion by MIF family members

Cell Signal. 2014 Dec;26(12):2969-78. doi: 10.1016/j.cellsig.2014.09.012. Epub 2014 Sep 30.

Abstract

Solid tumors are composed of a heterogeneous population of cells that interact with each other and with soluble and insoluble factors that, when combined, strongly influence the relative proliferation, differentiation, motility, matrix remodeling, metabolism and microvessel density of malignant lesions. One family of soluble factors that is becoming increasingly associated with pro-tumoral phenotypes within tumor microenvironments is that of the migration inhibitory factor family which includes its namesake, MIF, and its only known family member, D-dopachrome tautomerase (D-DT). This review seeks to highlight our current understanding of the relative contributions of a variety of immune and non-immune tumor stromal cell populations and, within those contexts, will summarize the literature associated with MIF and/or D-DT.

Keywords: Cancer; D-DT; Hypoxia; MIF; Stroma; Tumor microenvironment.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Disease Progression*
  • Humans
  • Intramolecular Oxidoreductases / metabolism
  • Macrophage Migration-Inhibitory Factors / metabolism*
  • Models, Biological
  • Neoplasms / enzymology
  • Neoplasms / metabolism*
  • Neoplasms / pathology*
  • Stromal Cells / enzymology
  • Stromal Cells / pathology

Substances

  • Macrophage Migration-Inhibitory Factors
  • Intramolecular Oxidoreductases
  • dopachrome isomerase