| Literature DB >> 31332789 |
Yuhong Chen1,2,3,4, Cuixia Di1,2,3,4, Xuetian Zhang1,2,3,4, Jing Wang5, Fang Wang1,2,3,4, Jun-Fang Yan1,2,3,4, Caipeng Xu1,2,3,4, Jinhua Zhang1,2,3,4, Qianjing Zhang1,2,3,4, Hongyan Li1,2,3,4, Hongying Yang6, Hong Zhang1,2,3,4.
Abstract
Transforming growth factor β (TGF-β) is part of the transforming growth factor β superfamily which is involved in many physiological processes and closely related to the carcinogenesis. Here, we discuss the TGF-β structure, function, and its canonical Smads signaling pathway. Importantly, TGF-β has been proved that it plays both tumor suppressor as well as an activator role in tumor progression. In an early stage, TGF-β inhibits cell proliferation and is involved in cell apoptosis. In an advanced tumor, TGF-β signaling pathway induces tumor invasion and metastasis through promoting angiogenesis, epithelial-mesenchymal transition, and immune escape. Furthermore, we are centered on updated research results into the inhibitors as drugs which have been studied in preclinical or clinical trials in tumor carcinogenesis to prevent the TGF-β synthesis and block its signaling pathways such as antibodies, antisense molecules, and small-molecule tyrosine kinase inhibitors. Thus, it is highlighting the crucial role of TGF-β in tumor therapy and may provide opportunities for the new antitumor strategies in patients with cancer.Entities:
Keywords: TGF-β; clinical application; drug; inhibitors; tumor
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Year: 2019 PMID: 31332789 DOI: 10.1002/jcp.29108
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384