| Literature DB >> 34299192 |
Jeff Yat-Fai Chung1, Max Kam-Kwan Chan1, Jane Siu-Fan Li1, Alex Siu-Wing Chan2, Philip Chiu-Tsun Tang1, Kam-Tong Leung3, Ka-Fai To1, Hui-Yao Lan4, Patrick Ming-Kuen Tang1.
Abstract
Transforming growth factor-β (TGF-β) signaling triggers diverse biological actions in inflammatory diseases. In tissue fibrosis, it acts as a key pathogenic regulator for promoting immunoregulation via controlling the activation, proliferation, and apoptosis of immunocytes. In cancer, it plays a critical role in tumor microenvironment (TME) for accelerating invasion, metastasis, angiogenesis, and immunosuppression. Increasing evidence suggest a pleiotropic nature of TGF-β signaling as a critical pathway for generating fibrotic TME, which contains numerous cancer-associated fibroblasts (CAFs), extracellular matrix proteins, and remodeling enzymes. Its pathogenic roles and working mechanisms in tumorigenesis are still largely unclear. Importantly, recent studies successfully demonstrated the clinical implications of fibrotic TME in cancer. This review systematically summarized the latest updates and discoveries of TGF-β signaling in the fibrotic TME.Entities:
Keywords: TGF-β; fibrosis; tumor microenvironment
Year: 2021 PMID: 34299192 DOI: 10.3390/ijms22147575
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923