巴基斯坦卢比
贝伐单抗
血管生成拟态
癌症研究
结直肠癌
医学
癌症
重编程
转录组
基因
染色体易位
化学
药理学
后天抵抗
癌细胞
细胞
作者
Weihao Li,Jianhong Peng,Jiahua He,Leen Liao,Da Kang,Weili Zhang,Weifeng Wang,Ruowei Wang,Song Wang,Yuanbin Liao,L Yu,Qingjian Ou,Yujing Fang,Xiaojun Wu,Peirong Ding,Zhizhong Pan,Chi Zhou,Junzhong Lin
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2026-03-05
卷期号:86 (11): 2759-2776
被引量:1
标识
DOI:10.1158/0008-5472.can-25-3520
摘要
Despite the clinical utility of bevacizumab in advanced colorectal cancer, resistance remains a major challenge. In this study, we unveiled a lactate-mediated mechanism driving vasculogenic mimicry (VM) and bevacizumab resistance through PKM2 lactylation. PKM2 lactylation at K206 by AARS1 promoted PKM2 nuclear translocation and interaction with FOSL1. PKM2 binding facilitated FOSL1-dependent super-enhancer formation and target gene transcription, which contributed to colorectal cancer cell VM. Genetic or pharmacologic inhibition of PKM2 lactylation disrupted VM and synergized with bevacizumab in patient-derived preclinical models, significantly improving therapeutic efficacy. Together, this study reveals lactylation as a metabolic switch linking cancer glycolytic reprogramming to transcriptional rewiring and proposes targeting PKM2 lactylation to enhance the antitumor activity of bevacizumab in colorectal cancer. SIGNIFICANCE: PKM2 lactylation mediates vasculogenic mimicry by facilitating FOSL1-dependent super-enhancer formation and represents a potential target to improve the clinical efficacy of bevacizumab in colorectal cancer patients.
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