TGFβ and activin A in the tumor microenvironment in colorectal cancer

被引:10
|
作者
Zessner-Spitzenberg, Jasmin [1 ,2 ]
Thomas, Alexandra L. [1 ]
Krett, Nancy L. [1 ]
Jung, Barbara [1 ]
机构
[1] Univ Illinois, Div Gastroenterol & Hepatol, Med Coll, Chicago, IL 60612 USA
[2] Med Univ Vienna, Spitalgasse 23, A-1090 Vienna, Austria
来源
GENE REPORTS | 2019年 / 17卷
基金
美国国家卫生研究院;
关键词
TGF beta; Activin A; Tumor microenvironment; Colorectal cancer; GROWTH-FACTOR-BETA; REGULATORY T-CELLS; DOWN-REGULATION; POOR-PROGNOSIS; METASTASIS; EXPRESSION; RECEPTOR; PROMOTES; PROTEIN; STROMA;
D O I
10.1016/j.genrep.2019.100501
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although overall survival in colorectal cancer (CRC) is increasing steadily due to progress in screening, therapeutic options and precise diagnostic tools remain scarce. As the understanding of CRC as a complex and multifactorial condition moves forward, the tumor microenvironment has come into focus as a source of diagnostic markers and potential therapeutic targets. The role of TGF beta in shifting the epithelial cancer compartment towards invasiveness and a pro-migratory phenotype via stromal signaling has been widely investigated. Accordingly, recent studies have proposed that CRC patients could be stratified into distinct subtypes and have identified one poor prognosis subset of CRC that is characterized by high stromal activity and elevated levels of TGF beta. The TGF beta superfamily member activin A is crucial for the pro-metastatic properties of the TGF beta pathway, yet it has been under-researched in CRC carcinogenesis. In this review, we will elucidate the signaling network and interdependency of both ligands in the context of the tumor microenvironment in CRC.
引用
收藏
页数:8
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