Recent Advances in the Development of TGF-β Signaling Inhibitors for Anticancer Therapy

被引:22
作者
Lee, Ho-Jae [1 ]
机构
[1] Gachon Univ, Lee Gil Ya Canc & Diabet Inst, Coll Med, Dept Biochem, Incheon, South Korea
基金
新加坡国家研究基金会;
关键词
TGF-beta; Tumor microenvironment; Tumor escape; Antineoplastic agents; Immune checkpoint inhibitors; GROWTH-FACTOR-BETA; EPITHELIAL-MESENCHYMAL TRANSITION; LY2157299; MONOHYDRATE; CANCER; RECEPTOR; EXPRESSION; MEMBRANE; PATHWAY; CELLS; PD-L1;
D O I
10.15430/JCP.2020.25.4.213
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
TGF-beta is a multifunctional cytokine that plays an important role in both physiologic and pathologic processes, including cancer. Importantly, TGF-beta has a dual role in tumorigenesis, acting as a tumor suppressor or a tumor promoter, depending on the stage of tumor development The aberrantly upregulated production of TGF-beta has been strongly implicated in tumor progression, angiogenesis, and metastasis, as well as immune evasion. Therefore, hyperactivated TGF-beta signaling is considered a potential therapeutic target for cancer therapy. Numerous inhibitors of overactivated TGF-beta signaling have been developed, and some of them are currently in clinical trials. This review focuses on the TGF-beta signaling that contributes to tumor progression and immune evasion in the tumor microenvironment and presents recent achievements on TGF-beta signaling inhibition as a single or combined therapeutic approach in cancer therapy.
引用
收藏
页码:213 / 222
页数:10
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