过氧化物酶体
脂质代谢
脂质体
棕榈酰化
过氧化物酶体增殖物激活受体
生物
生物化学
细胞生物学
硫酯酶
化学
癌症研究
受体
生物合成
半胱氨酸
酶
作者
Junqi Shan,Xinyu Li,Runqi Sun,Yao Yao,Yan Sun,Qin Kuang,Xianling Dai,Yanlai Sun
标识
DOI:10.1186/s13046-024-03154-0
摘要
The failure of proper recognition of the intricate nature of pathophysiology in colorectal cancer (CRC) has a substantial effect on the progress of developing novel medications and targeted therapy approaches. Imbalances in the processes of lipid oxidation and biosynthesis of fatty acids are significant risk factors for the development of CRC. Therapeutic intervention that specifically targets the peroxisome proliferator-activated receptor gamma (PPARγ) and its downstream response element, in response to lipid metabolism, has been found to promote the growth of tumors and has shown significant clinical advantages in cancer patients.
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