GCN5-ERK乳化-酸化循环放大了乳酸驱动的癌症进展
Bingsong Huang1,2, Mingpeng Jin3,4, Gaofeng Cui5
1Department of Neurosurgery, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, China.
Nature chemical biology
|January 13, 2026
概括
乳酸酸通过通过ERK乳化激活MAPK通路来加速癌症. 这项研究确定GCN5是负责酶和抑制剂,可以减少KRAS突变癌症的瘤生长.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 癌症研究 癌症研究
背景情况:
- 华堡效应增加了乳酸生产,通过不清楚的机制促进了癌症的进展.
- 乳酸在癌症进展中的作用需要了解其分子驱动因素.
研究的目的:
- 阐明将乳酸盐与癌症进展联系起来的分子机制.
- 为了确定关键的酶和途径参与乳酸介导的癌症生长.
- 开发和测试针对这种途径的治疗策略.
主要方法:
- 研究了乳酸在激活MAPK通路中的作用.
- 确定GCN5为ERK (细胞外信号调节激酶) 的乳酸转移酶.
- 评估了ERK乳化对ERK-MEK相互作用和激活的影响.
- 在癌症模型中开发和测试了ERK乳糖化细胞透抑制剂.
主要成果:
- 乳酸酸通过ERK乳化激活MAPK通路,促进癌症的进展.
- 鉴定出GCN5是负责ERK乳酸化的乳酸转移酶.
- 激活的ERK酸化了GCN5,形成了一个积极的反循环.
- 在K231处的ERK乳化减弱了ERK-MEK相互作用,增强了ERK的二分化和激活.
- 开发的抑制剂在KRAS突变癌症模型中的瘤生长受损.
结论:
- 乳酸盐通过ERK-GCN5乳化-酸化级联加速癌症的进展.
- 向ERK乳化为RAS-ERK驱动的癌症提供了潜在的治疗策略.
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