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细胞外囊泡来源的长链非编码RNA-GC1作为预测和监测胃癌患者免疫治疗结果的新型生物标志物。

Extracellular vesicle-derived lncRNA-GC1 serves as a novel biomarker for predicting and monitoring the immunotherapeutic outcomes of patients with gastric cancer.

作者信息

Wei Jiangpeng, Wang Xinxin, Dong Danhong, Ru Yi, Chen Lubin, Cheng Xin, Lv Xiaohui, Guo Xin

机构信息

Department of Digestive Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.

Department of General Surgery, Chinese PLA General Hospital, Beijing, China.

出版信息

BMC Med. 2025 Aug 27;23(1):499. doi: 10.1186/s12916-025-04270-0.

Abstract

BACKGROUND

Efforts to predict the outcomes of patients with gastric cancer (GC) following immune checkpoint inhibitor (ICI) treatments remain limited, owing to a lack of reliable biomarkers. Studies have found that extracellular vesicle (EV)-derived lncRNA-GC1 may serve as a GC-specific biomarker. This study was designed to expand on these previous results by estimating the usefulness of EV-derived lncRNA-GC1 as a predictive indicator for patients with GC who undergo ICI treatments.

METHODS

EV-derived lncRNA-GC1 levels were measured using real-time polymerase chain reaction (RT-PCR) in patients with unresectable or metastatic GC who were receiving ICI treatments. Correlations between this biomarker and ICI treatment outcomes were analyzed in a training cohort (n = 136), two external validation cohorts (n = 188 and n = 214), one expanding cohort (n = 30), and one prospective cohort (n = 192).

RESULTS

Circulating EVs exhibited a lncRNA-GC1 expression profile that was distinct from that of tissues or circulating cells. EV-derived lncRNA-GC1 levels were found to be independent of PD-L1 expression status or the density of CD8 T cell infiltration. EV-derived lncRNA-GC1 could be used to effectively predict ICI-related patient outcomes, and could be used for dynamic monitoring throughout treatments. Lower levels of EV-derived lncRNA-GC1 were associated with tumor microenvironmental characteristics such as more robust antitumor immunity-including higher levels of activated CD8 T/NK cells and an increased TH1/TH2 ratio. Such biomarkers can be stably detected in clinical practice. These results were consistent in both the two external validation cohorts and the one prospective cohort.

CONCLUSIONS

EV-derived lncRNA-GC1 can be used to reliably predict immunotherapeutic outcomes in patients with GC who undergo ICI treatments, suggesting that targeted analyses of this lncRNA may be useful for guiding treatment planning, monitoring, and associated decision-making processes.

摘要

背景

由于缺乏可靠的生物标志物,预测胃癌(GC)患者接受免疫检查点抑制剂(ICI)治疗后的结果的努力仍然有限。研究发现,细胞外囊泡(EV)衍生的lncRNA-GC1可能作为一种GC特异性生物标志物。本研究旨在通过评估EV衍生的lncRNA-GC1作为接受ICI治疗的GC患者的预测指标的有用性来扩展这些先前的结果。

方法

使用实时聚合酶链反应(RT-PCR)测量接受ICI治疗的不可切除或转移性GC患者中EV衍生的lncRNA-GC1水平。在一个训练队列(n = 136)、两个外部验证队列(n = 188和n = 214)、一个扩展队列(n = 30)和一个前瞻性队列(n = 192)中分析该生物标志物与ICI治疗结果之间的相关性。

结果

循环EV表现出与组织或循环细胞不同的lncRNA-GC1表达谱。发现EV衍生的lncRNA-GC1水平与PD-L1表达状态或CD8 T细胞浸润密度无关。EV衍生的lncRNA-GC1可用于有效预测ICI相关的患者结果,并可用于整个治疗过程中的动态监测。较低水平的EV衍生的lncRNA-GC1与肿瘤微环境特征相关,如更强的抗肿瘤免疫力,包括更高水平的活化CD8 T/NK细胞和增加的TH1/TH2比率。这种生物标志物可以在临床实践中稳定检测到。这些结果在两个外部验证队列和一个前瞻性队列中都是一致的。

结论

EV衍生的lncRNA-GC1可用于可靠地预测接受ICI治疗的GC患者的免疫治疗结果,表明对该lncRNA的靶向分析可能有助于指导治疗计划、监测和相关决策过程。

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