Transforming growth factor-beta1 and myeloid-derived suppressor cells: A cancerous partnership

Dev Dyn. 2022 Jan;251(1):105-124. doi: 10.1002/dvdy.339. Epub 2021 Apr 8.

Abstract

Transforming growth factor-beta1 (TGF-β1) plays a crucial role in tumor progression. It can inhibit early cancer stages but promotes tumor growth and development at the late stages of tumorigenesis. TGF-β1 has a potent immunosuppressive function within the tumor microenvironment that largely contributes to tumor cells' immune escape and reduction in cancer immunotherapy responses. Likewise, myeloid-derived suppressor cells (MDSCs) have been postulated as leading tumor promoters and a hallmark of cancer immune evasion mechanisms. This review attempts to analyze the prominent roles of both TGF-β1 and MDSCs and their interplay in cancer immunity. Furthermore, therapies against either TGF-β1 or MDSCs, and their potential synergistic combination with immunotherapies are discussed. Simultaneous TGF-β1 and MDSCs inhibition suggest a potential improvement in immunotherapy or subverted tumor immune resistance.

Keywords: MDSCs; T-cell immunosuppression; TGF-β1; cancer; myeloid-derived suppressor cells; tumor progression.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Humans
  • Myeloid-Derived Suppressor Cells* / pathology
  • Neoplasms* / pathology
  • Neoplasms* / therapy
  • Transforming Growth Factor beta1
  • Tumor Escape
  • Tumor Microenvironment

Substances

  • Transforming Growth Factor beta1