EPHX2 Inhibits Colon Cancer Progression by Promoting Fatty Acid Degradation

被引:21
作者
Zhou, Yiran [1 ,2 ]
Li, Xiao [1 ,2 ]
Guan, Aoran [1 ,2 ]
Zhou, Haodong [1 ,2 ]
Zhu, Yankun [1 ,2 ]
Wang, Ruotian [1 ,2 ]
Li, Ruhong [1 ,2 ]
机构
[1] Kunming Med Univ, Yanan Hosp Kunming City, Dept Gen Surg, Yanan Hosp, Kunming, Yunnan, Peoples R China
[2] Key Lab Tumor Immunol Prevent & Treatment Yunnan, Kunming, Yunnan, Peoples R China
关键词
EPHX2; CRC; metabolic reprogramming; fatty acid degradation; ROS; lipid droplet; SOLUBLE EPOXIDE HYDROLASE; METABOLISM; ROLES; CELLS;
D O I
10.3389/fonc.2022.870721
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor cells use metabolic reprogramming to keep up with the need for bioenergy, biosynthesis, and oxidation balance needed for rapid tumor division. This phenomenon is considered a marker of tumors, including colon cancer (CRC). As an important pathway of cellular energy metabolism, fatty acid metabolism plays an important role in cellular energy supply and oxidation balance, but presently, our understanding of the exact role of fatty acid metabolism in CRC is limited. Currently, no lipid metabolism therapy is available for the treatment of CRC. The establishment of a lipidmetabolism model regulated by oncogenes/tumor suppressor genes and associated with the clinical characteristics of CRC is necessary to further understand the mechanism of fatty acid metabolism in CRC. In this study, through multi-data combined with bioinformatic analysis and basic experiments, we introduced a tumor suppressor gene, EPHX2, which is rarely reported in CRC, and confirmed that its inhibitory effect on CRC is related to fatty acid degradation.
引用
收藏
页数:11
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