VCAM-1预测不良预后并调节胃癌的免疫透:基于TCGA的生物信息学研究
Cheng Wu1,2, Yungeng Liu1,2, Chuanyuan Liu1,2
1Department of Gastrointestinal and Hernia Surgery, Ganzhou Hospital-Nanfang Hospital, Southern Medical University, Ganzhou, China.
Frontiers in genetics
|September 10, 2025
概括
血管细胞粘附分子-1 (VCAM-1) 在胃癌中被上调,预测存活率较低,并影响瘤免疫微环境. VCAM-1可以通过调节免疫细胞透来优化胃癌免疫疗法.
科学领域:
- 在瘤学瘤学.
- 免疫学 免疫学 免疫学
- 分子生物学分子生物学
背景情况:
- 胃癌 (GC) 是癌症死亡的主要原因,预测免疫疗法耐药性的生物标志物有限.
- 血管细胞粘附分子-1 (VCAM-1) 参与瘤进展,但其在GC中的预后和免疫调节作用尚不清楚.
研究的目的:
- 研究VCAM-1表达在胃癌中的临床相关性和预后价值.
- 探索VCAM-1与GC中的瘤免疫微环境之间的关联.
主要方法:
- 来自癌症基因组图谱的RNA测序数据的分析,用于GC中的VCAM-1表达.
- 使用差异基因分析,基因组丰富分析 (GSEA) 和单样GSEA.
- 使用考克斯回归,ROC分析和来自人类蛋白质图谱数据库的免疫组织化学的验证结果.
主要成果:
- 在GC组织中,VCAM-1表达显著上调,与先进的T和N阶段以及较差的整体存活率相关.
- 根据GSEA的指示,VCAM-1与免疫通路 (如17-interleukin信号传递) 有关.
- 通过免疫组织化学证实,VCAM-1与Th1,细胞毒性和CD8+T细胞比例正相关,与Th17细胞相反.
结论:
- 在GC中,VCAM-1作为一种新的预后生物标志物,驱动一种免疫抑制瘤微环境.
- VCAM-1的双重免疫调节功能表明它有可能优化GC免疫疗法策略.
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