胶质瘤
生物
表观遗传学
重编程
癌症研究
血管生成
组蛋白
免疫疗法
调节器
癌基因
肿瘤进展
免疫系统
细胞周期
细胞生物学
细胞
癌症
免疫学
生物化学
遗传学
基因
作者
Tao Luo,Liang Liu,Hao Wang,Shuai Wen
标识
DOI:10.3892/ijo.2025.5764
摘要
Gliomas are the most common primary brain tumors, and exhibit highly heterogeneous and aggressive biological behaviors. Metabolic reprogramming is a hallmark of gliomas, and lactate accumulation serves a critical role in tumor progression. In addition to its traditional role as a metabolic byproduct, lactate has been recognized as a signaling molecule that modifies proteins through lactylation, which is a novel post‑translational modification. Lactate‑induced lactylation of histone and non‑histone proteins is emerging as a key epigenetic and metabolic regulator that influences glioma development, immune evasion, angiogenesis and therapeutic resistance. The present review provides mechanistic insights into protein lactylation, its role in glioma progression and its potential therapeutic implications. Targeting lactate metabolism and lactylation‑modifying enzymes holds promise for improving glioma treatment outcomes.
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