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Regulatory role of the transforming growth factor-β signaling pathway in the drug resistance of gastrointestinal cancers
Authors:Xiaoqun Lv  Guoxiong Xu
Affiliation:Department of Pharmacy, Jinshan Hospital, Fudan University, Shanghai 201508, China;Research Center for Clinical Medicine, Jinshan Hospital, Fudan University, Shanghai 201508, China;Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China. nc.ude.naduf@ux.gnoixoug
Abstract:Gastrointestinal (GI) cancer, including esophageal, gastric, and colorectal cancer, is one of the most prevalent types of malignant carcinoma and the leading cause of cancer-related deaths. Despite significant advances in therapeutic strategies for GI cancers in recent decades, drug resistance with various mechanisms remains the prevailing cause of therapy failure in GI cancers. Accumulating evidence has demonstrated that the transforming growth factor (TGF)-β signaling pathway has crucial, complex roles in many cellular functions related to drug resistance. This review summarizes current knowledge regarding the role of the TGF-β signaling pathway in the resistance of GI cancers to conventional chemotherapy, targeted therapy, immunotherapy, and traditional medicine. Various processes, including epithelial-mesenchymal transition, cancer stem cell development, tumor microenvironment alteration, and microRNA biogenesis, are proposed as the main mechanisms of TGF-β-mediated drug resistance in GI cancers. Several studies have already indicated the benefit of combining antitumor drugs with agents that suppress the TGF-β signaling pathway, but this approach needs to be verified in additional clinical studies. Moreover, the identification of potential biological markers that can be used to predict the response to TGF-β signaling pathway inhibitors during anticancer treatments will have important clinical implications in the future.
Keywords:Drug resistance, Gastrointestinal cancer, Transforming growth factor-β  , Epithelial-mesenchymal transition, Cancer stem cells, MicroRNAs
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