嘧啶代谢重塑免疫微环境,意味着胶质瘤预后不良。

IF 2.8 3区 医学 Q2 ONCOLOGY Clinical & Translational Oncology Pub Date : 2024-10-16 DOI:10.1007/s12094-024-03753-5
Ruoyu Huang, Jingchen Yang, Xuejing Li, Huiyuan Chen, Xing Liu
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引用次数: 0

摘要

背景:胶质瘤的代谢环境极其复杂。嘧啶代谢可显著影响多种癌细胞的恶性进展。本研究旨在探讨嘧啶代谢与胶质瘤恶性进展之间的关系:方法:我们分析了两个胶质瘤 RNA 序列数据库,构建了嘧啶代谢相关风险特征。方法:我们分析了两个胶质瘤 RNA 序列数据库,构建了一个嘧啶代谢相关风险特征,并基于该风险特征建立了一个个体化预后预测模型。通过功能分析和体外实验评估了嘧啶代谢在肿瘤免疫微环境和胶质瘤恶性进展中的作用:结果:根据嘧啶代谢相关风险评分预测,高危组有恶性程度更高、生存率更低的趋势。功能分析显示,嘧啶代谢对肿瘤免疫微环境有显著调节作用。体外实验证实,靶向嘧啶代谢相关基因可抑制胶质瘤细胞的恶性程度:总之,我们建立的嘧啶代谢相关特征可作为弥漫性胶质瘤的独立预后生物标志物,并与肿瘤免疫微环境调控密切相关。
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Pyrimidine metabolism reshapes immune microenvironment and implies poor prognosis in glioma.

Background: The metabolic environment of glioma is extremely complex. Pyrimidine metabolism can significantly influence malignant progression of multiple kinds of cancer cells. In this study, we intend to explore the relationship between pyrimidine metabolism and malignant progression of glioma.

Methods: We analyzed two glioma RNA-sequencing databases to construct a pyrimidine metabolism-related risk signature. An individualized prognosis prediction model based on this risk signature was established. Functional analysis and in vitro experiments were conducted to assess the role of pyrimidine metabolism in the tumor-immune microenvironment and malignant progress of gliomas.

Results: The high-risk group, as predicted by the pyrimidine metabolism-related risk score, showed a tendency toward more malignant entities and poorer survival outcomes. Functional analysis revealed that pyrimidine metabolism significantly regulates the tumor-immune microenvironment. In vitro experiments confirmed that targeting pyrimidine metabolism-related genes can inhibit malignancy of glioma cell.

Conclusion: In short, the pyrimidine metabolism-related signature we established could serve as an independent prognostic biomarker in diffuse gliomas and has a close association with regulation of the tumor-immune microenvironment.

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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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