Roles of peroxisome proliferator-activated receptors in hepatocellular carcinoma

被引:5
|
作者
Zhao, Yaqin [1 ]
Tan, Huabing [2 ]
Zhang, Xiaoyu [3 ]
Zhu, Jing [4 ,5 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Dept Abdominal Oncol, Chengdu, Peoples R China
[2] Hubei Univ Med, Renmin Hosp, Dept Infect Dis, Liver Dis Lab, Shiyan, Hubei, Peoples R China
[3] Xuzhou Med Univ, Affiliated Huaian Hosp, Dept Gen Surg, Div Gastrointestinal Surg, Huaian, Peoples R China
[4] Nanjing Drum Tower Hosp, Nanjing, Peoples R China
[5] Nanjing Drum Tower Hosp, Dept Oncol, Nanjing, Peoples R China
关键词
HCC; NAFLD; peroxisome proliferator-activated receptor (PPAR); prognosis; FATTY LIVER-DISEASE; PPAR-GAMMA; CELL-PROLIFERATION; HEPATIC STEATOSIS; LIPID-METABOLISM; ALPHA; TUMORIGENESIS; PROGRESSION; CANCER; GROWTH;
D O I
10.1111/jcmm.18042
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hepatocellular carcinoma (HCC), the main pathological type of liver cancer, is linked to risk factors such as viral hepatitis, alcohol intake and non-alcoholic fatty liver disease (NAFLD). Recent advances have greatly improved our understanding that NAFLD is playing a major risk factor for HCC. Peroxisome proliferator-activated receptors (PPARs) are a class of transcription factors divided into three subtypes: PPAR alpha (PPARA), PPAR delta/beta (PPARD) and PPAR gamma (PPARG). As important nuclear receptors, PPARs are involved in many physiological processes, and PPARs can improve NAFLD by regulating lipid metabolism, accelerating fatty acid oxidation and inhibiting inflammation. In recent years, some studies have shown that PPARs can participate in the occurrence and development of HCC by regulating metabolic pathways. In addition, PPAR modulators have been reported to inhibit the proliferation and metastasis of HCC cells and can enhance the curative effect of conventional treatments. This article reviews the role of PPARs in the occurrence and development of HCC, as well as its value in the diagnosis, treatment and prognosis of HCC, in order to provide directions for future research.
引用
收藏
页数:12
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