Role and clinical significance of TGF‑β1 and TGF‑βR1 in malignant tumors (Review)

Int J Mol Med. 2021 Apr;47(4):55. doi: 10.3892/ijmm.2021.4888. Epub 2021 Feb 19.

Abstract

The appearance and growth of malignant tumors is a complicated process that is regulated by a number of genes. In recent years, studies have revealed that the transforming growth factor‑β (TGF‑β) signaling pathway serves an important role in cell cycle regulation, growth and development, differentiation, extracellular matrix synthesis and immune response. Notably, two members of the TGF‑β signaling pathway, TGF‑β1 and TGF‑β receptor 1 (TGF‑βR1), are highly expressed in a variety of tumors, such as breast cancer, colon cancer, gastric cancer and hepatocellular carcinoma. Moreover, an increasing number of studies have demonstrated that TGF‑β1 and TGF‑βR1 promote proliferation, migration and epithelial‑mesenchymal transition of tumor cells by activating other signaling pathways, signaling molecules or microRNAs (miRs), such as the NF‑κB signaling pathway and miR‑133b. In addition, some inhibitors targeting TGF‑β1 and TGF‑βR1 have exhibited positive effects in in vitro experiments. The present review discusses the association between TGF‑β1 or TGF‑βR1 and tumors, and the development of some inhibitors, hoping to provide more approaches to help identify novel tumor markers to restrain and cure tumors.

Keywords: transforming growth factor‑β1; transforming growth factor‑β receptor 1; malignant tumor.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Carcinogenesis / pathology*
  • Cell Cycle / genetics
  • Cell Differentiation / genetics
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Epithelial-Mesenchymal Transition / genetics
  • Humans
  • MicroRNAs / genetics
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Neoplasms / pathology*
  • Receptor, Transforming Growth Factor-beta Type I / antagonists & inhibitors
  • Receptor, Transforming Growth Factor-beta Type I / genetics
  • Receptor, Transforming Growth Factor-beta Type I / metabolism*
  • Signal Transduction
  • Transforming Growth Factor beta1 / antagonists & inhibitors
  • Transforming Growth Factor beta1 / genetics
  • Transforming Growth Factor beta1 / metabolism*

Substances

  • Biomarkers, Tumor
  • MicroRNAs
  • TGFB1 protein, human
  • Transforming Growth Factor beta1
  • Receptor, Transforming Growth Factor-beta Type I
  • TGFBR1 protein, human

Grants and funding

The present review was supported by the National Natural Science Foundation of China (grant no. 81873076) and the Shanghai Talents Development Fund Project in China (grant no. 2017090).