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卵巢癌转录组分析揭示肿瘤相关炎症/免疫与患者预后之间的关联

英文原题:Transcriptome analysis of ovarian cancer uncovers association between tumor-related inflammation/immunity and patient outcome.

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Transcriptome analysis of ovarian cancer uncovers association between tumor-related inflammation/immunity and patient outcome.

PubMed 2025/02/06(内容时间) Front Pharmacol Q1 · IF 5.4(JCR 2025)

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研究概要

这些发现为卵巢癌的免疫治疗和预后评估提供了新的视角和潜在靶点,并为临床治疗和患者管理提供了新的策略和方向。本研究为进一步理解药物反应机制和肿瘤免疫治疗提供了关键信息。它为卵巢癌的治疗和预后改善提供了新的策略和方法。

研究思路结论见上方概要

上皮性卵巢癌(EOC)是一种影响女性生殖系统的癌症,致死率很高。它在治疗方面面临重大挑战,且往往预后不良。近年来,随着 PARPi 的出现,卵巢癌的治疗进入了全程管理的新阶段。尽管越来越多的药物获批,但 PARPi 的治疗效果仍然非常有限。随着 PD-1/PD-L1、CTLA-4、溶瘤病毒、癌症疫苗、过继细胞疗法等的快速发展,肿瘤免疫治疗为卵巢癌的治疗提供了新的机遇。

本研究利用多个数据库的综合转录组分析,收集正常卵巢样本和卵巢癌组织样本的基因转录本及临床特征,旨在探究肿瘤免疫治疗耐药的机制,并揭示卵巢癌免疫微环境与炎症相关基因之间的关系。研究使用多种R包进行差异基因分析、富集分析、共表达网络构建和预后模型构建。

研究发现,卵巢癌患者的预后与参与炎症的基因集密切相关。通过聚类和免疫微环境分析确定的两种炎症基因表达模式在免疫浸润微环境、临床病理特征和生存率方面存在显著差异。进一步分析显示,高风险组具有更高丰度的M2型巨噬细胞浸润、更活跃的抗肿瘤免疫反应、更高的肿瘤干性评分、可能更差的预后,以及对多种化疗药物和免疫检查点抑制剂的缓解率较低。

展开英文摘要原文

Epithelial ovarian cancer (EOC) is a cancer that affects the female reproductive system and is highly lethal. It poses significant challenges in terms of treatment and often has a poor prognosis. In recent years, with the advent of PARPi, the treatment of ovarian cancer has entered a new stage of full-process management. Although more and more drugs have been approved, the therapeutic effect of PARPi is still very limited. With the rapid development of PD-1/PD-L1, CTLA-4, oncolytic viruses, cancer vaccines, adoptive cell therapy, etc., tumor immunotherapy has provided new opportunities for the treatment of ovarian cancer.

This study used comprehensive transcriptome analysis across multiple databases to gather gene transcripts and clinical features of normal ovarian samples and tissue samples from ovarian cancer. The aim was to explore the mechanisms underlying tumor immunotherapy resistance and to reveal the relationship between ovarian cancer's immune microenvironment and genes linked to inflammation. Various R packages were used for differential gene analysis, enrichment analysis, co-expression network construction, and prognostic model building.

It has been found that the prognosis of ovarian cancer patients is closely associated with sets of genes involved in inflammation. The immune infiltration microenvironment, clinicopathological features, and survival rates differed significantly between two inflammatory gene expression patterns identified using cluster and immune microenvironment analyses. Further analysis revealed that the high-risk group had a higher abundance of M2-type macrophage infiltration, more active anti-tumor immune response, higher tumor stemness score, potentially worse prognosis, and lower response rates to multiple chemotherapy drugs and immune checkpoint inhibitors.

These findings provide new perspectives and potential targets for immunotherapy and prognostic evaluation of ovarian cancer and offer new strategies and directions for clinical treatment and patient management. This study provides crucial information to further our comprehension of drug response mechanisms and tumor immunotherapy. It offers new strategies and methods for the treatment and prognostic improvement of ovarian cancer.

论文信息

作者
Wang J、Zhu W、Li X、Wu Y、Ma W、Wang Y、Zhao W、Wei F
单位
Department of Obstetrics and Gynecology, Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.China
期刊
Frontiers in pharmacology2025
原文标识
PubMed 39981173 · DOI 10.3389/fphar.2025.1500251