Immunomodulatory TGF-β Signaling in Hepatocellular Carcinoma

被引:191
|
作者
Chen, Jian [1 ]
Gingold, Julian A. [2 ]
Su, Xiaoping [3 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gastroenterol Hepatol & Nutr, Houston, TX 77030 USA
[2] Cleveland Clin Fdn, Womens Hlth Inst, 9500 Euclid Ave, Cleveland, OH 44195 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Bioinformat, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Computat Biol, Houston, TX 77030 USA
关键词
GROWTH-FACTOR-BETA; REGULATORY T-CELLS; GENE-EXPRESSION; THERAPEUTIC IMPLICATIONS; ADOPTIVE IMMUNOTHERAPY; CANCER-IMMUNOTHERAPY; TUMOR SUPPRESSION; IMMUNE CELLS; SORAFENIB; LANDSCAPE;
D O I
10.1016/j.molmed.2019.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatocellular carcinoma (HCC) is an inflammation-induced and chemotherapy-resistant cancer. Dysregulated signaling in the transforming growth factor beta (TGF-beta) pathway plays a central role in inflammation, fibrogenesis, and immunomodulation in the HCC microenvironment. This review dissects the genetic landscape of the TGF-beta superfamily genes in HCC and discusses the essential effects of this pathway on the tumor immune microenvironment. We highlight the TGF-beta signature as a potential biomarker for identifying individualized immunotherapeutic approaches in HCC. An improved understanding of the detailed mechanisms of liver cancer immunogenicity and the specific role of TGF-beta in mediating immunotherapy resistance in HCC will provide important insights into HCC immune escape and promote the development of biomarker-derived combination immunotherapies for HCC.
引用
收藏
页码:1010 / 1023
页数:14
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