综合应激反应途径协调了肺癌多个免疫检查点的翻译控制
Shayna Thomas-Jardin1, Shruthy Suresh2, Ariana Arce1
1The University of Texas Southwestern Medical Center, Dallas, TX, United States.
综合应激反应 (ISR) 途径通过增加PD-L1和CD155.5等免疫检查点来帮助癌细胞存活. 抑制ISR可能提供一种新的肺癌治疗策略.
科学领域:
- 免疫学 免疫学 免疫学
- 癌症生物学 癌症生物学
- 分子生物学分子生物学
背景情况:
- 综合应激反应 (ISR) 对瘤微环境中的癌细胞存活至关重要.
- 通过诱导编程死亡连接体1 (PD-L1),ISR激活促进瘤免疫逃避.
研究的目的:
- 为了识别由ISR调节的额外免疫检查点蛋白质.
- 为了阐明瘤免疫逃逸的ISR介导机制.
主要方法:
- 研究了免疫检查点的ISR协调调节.
- 通过5' UTRs分析了PD-L1和CD155的翻译增强.
- 在人类肺瘤中相关的PD-L1和CD155表达.
主要成果:
- ISR协调诱导了CD155和PD-L1的表达.
- 通过绕过上游开放的阅读框架来增强CD155和PD-L1的翻译.
- 在初级肺瘤中发现PD-L1和CD155之间存在显著的相关性.
- ISR激活加速了瘤生长和T细胞功能受损.
结论:
- 该ISR协调多个免疫检查点的表达,包括PD-L1和CD155.5.
- 联合阻断PD-1,TIGIT和ISR抑制 (ISRIB) 可以克服ISR驱动的瘤免疫逃逸.
- 这项研究提出了针对ISR的肺癌新型治疗策略.
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