肝肠循环
法尼甾体X受体
熊去氧胆酸
肝细胞癌
胆汁酸
硼胆酸
生物
CYP8B1
癌症研究
核受体
内科学
医学
受体
内分泌学
生物化学
胆固醇7α羟化酶
转录因子
基因
兴奋剂
作者
Wenyu Luo,Shiqi Guo,Yang Zhou,Junfeng Zhu,Jialong Zhao,M. Wang,Li-Xuan Sang,Bingyuan Wang,Bing Chang
标识
DOI:10.3892/ijo.2022.5407
摘要
Bile acids (BAs) are the major components of bile and products of cholesterol metabolism. Cholesterol is catalyzed by a variety of enzymes in the liver to form primary BAs, which are excreted into the intestine with bile, and secondary BAs are formed under the modification of the gut microbiota. Most of the BAs return to the liver via the portal vein, completing the process of enterohepatic circulation. BAs have an important role in the development of hepatocellular carcinoma (HCC), which may participate in the progression of HCC by recognizing receptors such as farnesoid X receptor (FXR) and mediating multiple downstream pathways. Certain BAs, such as ursodeoxycholic acid and obeticholic acid, were indicated to be able to delay liver injury and HCC progression. In the present review, the structure and function of BAs were introduced and the metabolism of BAs and the process of enterohepatic circulation were outlined. Furthermore, the mechanisms by which BAs participate in the development of HCC were summarized and possible strategies for targeting BAs and key sites of their metabolic processes to treat HCC were suggested.
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