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通过单细胞 RNA-seq 和 bulk RNA-seq 整合分析建立卵巢癌耗竭 CD8+T 细胞相关基因模型。

Establishment of an ovarian cancer exhausted CD8+T cells-related genes model by integrated analysis of scRNA-seq and bulk RNA-seq.

机构信息

Department of Gynecology, Affiliated Xingtai People Hospital of Hebei Medical University, Xingtai, China.

Department of Oncology, Affiliated Xingtai People Hospital of Hebei Medical University, 16 Hongxing Road, Xingtai, Hebei, 054001, People's Republic of China.

出版信息

Eur J Med Res. 2024 Jul 5;29(1):358. doi: 10.1186/s40001-024-01948-8.

Abstract

Ovarian cancer (OC) was the fifth leading cause of cancer death and the deadliest gynecological cancer in women. This was largely attributed to its late diagnosis, high therapeutic resistance, and a dearth of effective treatments. Clinical and preclinical studies have revealed that tumor-infiltrating CD8+T cells often lost their effector function, the dysfunctional state of CD8+T cells was known as exhaustion. Our objective was to identify genes associated with exhausted CD8+T cells (CD8TEXGs) and their prognostic significance in OC. We downloaded the RNA-seq and clinical data from the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases. CD8TEXGs were initially identified from single-cell RNA-seq (scRNA-seq) datasets, then univariate Cox regression, the least absolute shrinkage and selection operator (LASSO), and multivariate Cox regression were utilized to calculate risk score and to develop the CD8TEXGs risk signature. Kaplan-Meier analysis, univariate Cox regression, multivariate Cox regression, time-dependent receiver operating characteristics (ROC), nomogram, and calibration were conducted to verify and evaluate the risk signature. Gene set enrichment analyses (GSEA) in the risk groups were used to figure out the closely correlated pathways with the risk group. The role of risk score has been further explored in the homologous recombination repair deficiency (HRD), BRAC1/2 gene mutations and tumor mutation burden (TMB). A risk signature with 4 CD8TEXGs in OC was finally built in the TCGA database and further validated in large GEO cohorts. The signature also demonstrated broad applicability across various types of cancer in the pan-cancer analysis. The high-risk score was significantly associated with a worse prognosis and the risk score was proven to be an independent prognostic biomarker. The 1-, 3-, and 5-years ROC values, nomogram, calibration, and comparison with the previously published models confirmed the excellent prediction power of this model. The low-risk group patients tended to exhibit a higher HRD score, BRCA1/2 gene mutation ratio and TMB. The low-risk group patients were more sensitive to Poly-ADP-ribose polymerase inhibitors (PARPi). Our findings of the prognostic value of CD8TEXGs in prognosis and drug response provided valuable insights into the molecular mechanisms and clinical management of OC.

摘要

卵巢癌(OC)是女性癌症死亡的第五大主要原因,也是最致命的妇科癌症。这在很大程度上归因于其晚期诊断、高治疗耐药性和缺乏有效治疗方法。临床和临床前研究表明,肿瘤浸润 CD8+T 细胞通常会失去其效应功能,CD8+T 细胞的功能障碍状态被称为衰竭。我们的目标是鉴定与衰竭的 CD8+T 细胞(CD8TEXGs)相关的基因及其在 OC 中的预后意义。我们从癌症基因组图谱(TCGA)和基因表达综合数据库(GEO)下载了 RNA-seq 和临床数据。首先从单细胞 RNA-seq(scRNA-seq)数据集鉴定 CD8TEXGs,然后使用单因素 Cox 回归、最小绝对收缩和选择算子(LASSO)以及多因素 Cox 回归计算风险评分并开发 CD8TEXGs 风险特征。进行 Kaplan-Meier 分析、单因素 Cox 回归、多因素 Cox 回归、时间依赖性接收者操作特征(ROC)、列线图和校准以验证和评估风险特征。风险组中的基因集富集分析(GSEA)用于找出与风险组密切相关的途径。在同源重组修复缺陷(HRD)、BRAC1/2 基因突变和肿瘤突变负担(TMB)中进一步探讨了风险评分的作用。最终在 TCGA 数据库中构建了一个包含 4 个 OC CD8TEXGs 的风险特征,并在大型 GEO 队列中进一步验证。该特征在泛癌分析中也表现出在各种类型癌症中的广泛适用性。高风险评分与预后较差显著相关,风险评分被证明是独立的预后生物标志物。1 年、3 年和 5 年 ROC 值、列线图、校准和与之前发表的模型的比较证实了该模型的出色预测能力。低风险组患者倾向于表现出更高的 HRD 评分、BRCA1/2 基因突变率和 TMB。低风险组患者对聚 ADP-核糖聚合酶抑制剂(PARPi)更敏感。我们对 CD8TEXGs 在预后和药物反应中的预后价值的研究结果为 OC 的分子机制和临床管理提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/446c/11225302/4bbf16afb3dd/40001_2024_1948_Fig1_HTML.jpg

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