结直肠癌
重编程
生物
癌变
脂质代谢
调节器
线粒体融合
癌症研究
细胞生物学
线粒体
癌症
平衡
下调和上调
脂肪酸合酶
酶
生物化学
细胞生长
硬脂酸
脂滴
新陈代谢
丁酸盐
脂肪酸代谢
体外
脂肪组织
融合蛋白
代谢途径
焊剂(冶金)
癌细胞
甾醇调节元件结合蛋白
基因表达调控
作者
Zhiqian Bi,Xiaoyao Chang,Shengyun Zhu,Shuilian Fu,Yuzhe Zhang,Tingting Wang,Feng Wang,Hongqin Zhuang,Zi-Chun Hua
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-02-13
卷期号:12 (7): eadz2892-eadz2892
标识
DOI:10.1126/sciadv.adz2892
摘要
Lipid metabolic reprogramming is a hallmark of colorectal cancer (CRC), yet the precise molecular mechanisms underlying lipid-mediated oncogenesis and the specific lipid metabolic enzymes involved remain largely elusive. Here, we identify elongation of very-long-chain fatty acid protein 6 (Elovl6) as a critical regulator in CRC progression. Clinical data reveal significant down-regulation of Elovl6 in colon cancer tissues, with low expression levels correlating with unfavorable patient prognosis. We demonstrate that Elovl6 exerts potent tumor-suppressive effects, significantly inhibiting cellular proliferation in vitro and attenuating tumor growth in vivo. Mechanistically, it maintains intestinal microbial homeostasis by preventing the expansion of opportunistic pathogens while simultaneously orchestrating metabolic reprogramming through modulation of phospholipid biosynthesis pathways. Notably, we find that stearic acid, a key Elovl6-derived metabolite, promotes mitochondrial fusion by stabilizing mitofusin 1 protein. These findings not only position Elovl6 as a promising therapeutic target but also suggest that dietary supplementation with stearic acid could represent a viable strategy for CRC prevention and treatment.
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