磷脂酰肌醇
转录组
花生四烯酸
细胞生物学
生物
二十烷酸
脂质代谢
沙盒(软件开发)
糖酵解
生物化学
类有机物
基因表达调控
信号转导
二酰甘油激酶
细胞分化
基因
基因表达
脂毒性
新陈代谢
化学
脂肪酸
激酶
代谢途径
脂质信号
结直肠癌
作者
Albert Maimo-Barcelo,Joan Bestard-Escalas,Karim Perez-Romero,Lucia Martin-Saiz,Josep Muncunill-Fortuny,Catalina Crespi,Marco A. Olivera Martínez,L. A. Martin,Daniel H. López,Gonzalo P. Martin,José Manuel Olea,José A. Fernández,Ramón María Alvargonzález Rodríguez,Gwendolyn Barceló‐Coblijn
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2026-02-22
标识
DOI:10.64898/2026.02.20.706976
摘要
ABSTRACT Membrane lipid composition changes concomitantly with human colonocyte differentiation, a tightly regulated process occurring along the colon crypt. This process is heavily disrupted in colon cancer. Nonetheless, the regulatory mechanisms driving these changes, especially the replacement of arachidonic acid phosphatidylinositol species with monounsaturated fatty acid species, and how they are altered in cancer, remain unknown. To establish the transcriptional networks underlying this remodeling, we integrated transcriptomic and lipidomic profiles of isolated healthy and tumor human colonocytes using system biology approaches; identifying key gene regulatory networks involved in arachidonic acid and eicosanoid metabolism and phosphatidylinositol cycle as significant regulators during differentiation. Consistently, a distinct impact was found on organoid differentiation depending on colonocyte subtype and specific prostaglandin. Remarkably, the shift and associated transcriptomic programs were lost in tumor that heightened phosphoinositide metabolism. Altogether, these results underscore the importance of lipid remodeling in colonocyte stemness maintenance and proper onset of differentiation programs.
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