The Role of HSF1 and the Chaperone Network in the Tumor Microenvironment

Adv Exp Med Biol. 2020:1243:101-111. doi: 10.1007/978-3-030-40204-4_7.

Abstract

Tumors are stressful environments. As tumors evolve from single mutated cancer cells into invasive malignancies they must overcome various constraints and barriers imposed by a hostile microenvironment. To achieve this, cancer cells recruit and rewire cells in their microenvironment to become pro-tumorigenic. We propose that chaperones are vital players in this process, and that activation of stress responses helps tumors adapt and evolve into aggressive malignancies, by enabling phenotypic plasticity in the tumor microenvironment (TME). In this chapter we will review evidence supporting non-cancer-cell-autonomous activity of chaperones in human patients and mouse models of cancer, discuss the mechanisms by which this non-cell-autonomous activity is mediated and provide an evolutionary perspective on the basis of this phenomenon.

Keywords: Cancer; Cancer-associated fibroblasts; Chaperones; ER-stress; HSF1; Heat shock; Stress responses; Tumor microenvironment; UPR.

Publication types

  • Review

MeSH terms

  • Animals
  • Carcinogenesis
  • Heat Shock Transcription Factors / metabolism*
  • Humans
  • Molecular Chaperones / metabolism*
  • Neoplasms / genetics
  • Neoplasms / metabolism*
  • Tumor Microenvironment* / genetics

Substances

  • HSF1 protein, human
  • Heat Shock Transcription Factors
  • Molecular Chaperones