Xia Yan, Lin Xin, Cheng Yangyang, Xu Huimin, Zeng Jingya, Xie Wanlin, Wang Mingzhu, Sun Yihua
Department of Clinical Laboratory, Harbin Medical University Cancer Hospital, Harbin, China.
Scientific Research Center, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Front Genet. 2022 Jun 28;13:938796. doi: 10.3389/fgene.2022.938796. eCollection 2022.
Immunotherapy is widely used to treat various cancers, but patients with gastric cancer (GC), which has a high mortality rate, benefit relatively less from this therapy. Platelets are closely related to GC progression and metastasis. This study aimed to find novel potential biomarkers related to platelet function to predict GC and immunotherapy efficacy. First, based on platelet activation, signaling, and aggregation (abbreviation: function)-related genes (PFRGs), we used the least absolute shrinkage and selection operator (Lasso) regression method to construct a platelet-function-related genes prognostic score (PFRGPS). PRFGPS was verified in three independent external datasets (GSE26901, GSE15459, and GSE84437) for its robustness and strong prediction performance. Our results demonstrate that PRFGPS is an independent prognostic indicator for predicting overall survival in patients with GC. In addition, prognosis, potential pathogenesis mechanisms, and the response to immunotherapy were defined via gene set enrichment analysis, tumor mutational burden, tumor microenvironment, tumor immune dysfunction and exclusion (TIDE), microsatellite instability, and immune checkpoint inhibitors. We found that the high-PRFGPS subgroup had a cancer-friendly immune microenvironment, a high TIDE score, a low tumor mutational burden, and relatively low microsatellite instability. In the immunophenoscore model, the therapeutic effect on anti-PD-1 and anti-CTLA-4 in the high-PRFGPS subgroup was relatively low. In conclusion, PRFGPS could be used as a reference index for GC prognosis to develop more successful immunotherapy strategies.
免疫疗法被广泛用于治疗各种癌症,但胃癌(GC)患者的死亡率很高,从这种疗法中获益相对较少。血小板与GC的进展和转移密切相关。本研究旨在寻找与血小板功能相关的新型潜在生物标志物,以预测GC和免疫治疗疗效。首先,基于血小板激活、信号传导和聚集(缩写:功能)相关基因(PFRGs),我们使用最小绝对收缩和选择算子(Lasso)回归方法构建了血小板功能相关基因预后评分(PFRGPS)。PFRGPS在三个独立的外部数据集(GSE26901、GSE15459和GSE84437)中得到验证,证明其具有稳健性和强大的预测性能。我们的结果表明,PFRGPS是预测GC患者总生存的独立预后指标。此外,通过基因集富集分析、肿瘤突变负担、肿瘤微环境、肿瘤免疫功能障碍和排除(TIDE)、微卫星不稳定性和免疫检查点抑制剂来确定预后、潜在发病机制和对免疫治疗的反应。我们发现,高PFRGPS亚组具有有利于癌症的免疫微环境、高TIDE评分、低肿瘤突变负担和相对较低的微卫星不稳定性。在免疫表型评分模型中,高PFRGPS亚组对抗PD-1和抗CTLA-4的治疗效果相对较低。总之,PFRGPS可作为GC预后的参考指标,以制定更成功的免疫治疗策略。