局部晚期直肠癌新辅助放化疗期间血清代谢物的LC-MS代谢组学分析

IF 2.8 3区 医学 Q2 ONCOLOGY
Clinical & Translational Oncology Pub Date : 2024-12-01 Epub Date: 2024-06-03 DOI:10.1007/s12094-024-03537-x
Qiliang Peng, Lili Jiang, Yi Shen, Yao Xu, Xinan Shen, Li Zou, Yaqun Zhu, Yuntian Shen
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引用次数: 0

摘要

研究背景本研究旨在利用液相色谱-质谱(LC-MS)代谢组学分析方法,研究局部晚期直肠癌(LARC)患者新辅助化放疗(NCRT)期间的血清代谢物谱。方法:从放疗前、放疗中和放疗后的 20 名 LARC 患者中采集 60 份血清样本,进行 LC-MS 代谢组学分析,以确定代谢物的变化。应用功能注释发现代谢途径的改变。筛选出关键代谢物,并利用随机森林和 ROC 曲线计算其预测放疗敏感性的能力:结果表明,NCRT 导致血清代谢物谱发生显著变化。血清代谢谱在不同时间点和不同敏感性组之间有明显的分离。此外,功能注释显示,不同的代谢物与一系列重要的代谢途径相关。放疗前的(3Z,6Z)-3,6-壬二烯纳和放疗前的1-羟基布洛芬在区分NCRT敏感组和非敏感组方面显示出良好的预测性能,AUC分别为0.812和0.75。重要的是,不同代谢物的组合能显著提高预测能力:这项研究证明了 LC-MS 代谢组学在揭示 LARC NCRT 期间血清代谢物谱方面的潜力。鉴定出的代谢物可作为治疗该疾病的潜在生物标记物和治疗靶点。此外,了解受影响的代谢途径有助于为 LARC 患者设计更加个性化的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

LC-MS metabolomics analysis of serum metabolites during neoadjuvant chemoradiotherapy in locally advanced rectal cancer.

LC-MS metabolomics analysis of serum metabolites during neoadjuvant chemoradiotherapy in locally advanced rectal cancer.

Background: This study aimed to investigate the serum metabolite profiles during neoadjuvant chemoradiotherapy (NCRT) in locally advanced rectal cancer (LARC) using liquid chromatography-mass spectrometry (LC-MS) metabolomics analysis.

Methods: 60 serum samples were collected from 20 patients with LARC before, during, and after radiotherapy. LC-MS metabolomics analysis was performed to identify the metabolite variations. Functional annotation was applied to discover altered metabolic pathways. The key metabolites were screened and their ability to predict sensitivity to radiotherapy was calculated using random forests and ROC curves.

Results: The results showed that NCRT led to significant changes in the serum metabolite profiles. The serum metabolic profiles showed an apparent separation between different time points and different sensitivity groups. Moreover, the functional annotation showed that the differential metabolites were associated with a series of important metabolic pathways. Pre-radiotherapy (3Z,6Z)-3,6-Nonadiena and pro-radiotherapy 1-Hydroxyibuprofen showed good predictive performance in discriminating the sensitive and non-sensitive group to NCRT, with an AUC of 0.812 and 0.75, respectively. Importantly, the combination of different metabolites significantly increased the predictive ability.

Conclusion: This study demonstrated the potential of LC-MS metabolomics for revealing the serum metabolite profiles during NCRT in LARC. The identified metabolites may serve as potential biomarkers and therapeutic targets for the management of this disease. Furthermore, the understanding of the affected metabolic pathways may help design more personalized therapeutic strategies for LARC patients.

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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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