血浆代谢组学检测结直肠癌的新生物标志物的发现和验证

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2025-06-06 DOI:10.1002/mco2.70201
Jianv Huang, Le Wang, Xiang Zhang, Xinyi Liu, Junyan Miao, Yuefan Shen, Chengqu Fu, Xianxiu Ge, Xue Wang, Jiancong Hu, Guanman Li, Yang Sun, Yinglei Miao, Juncheng Dai, Lingbin Du, Hongxia Ma, Guangfu Jin, Ni Li, Lin Miao, Zhibin Hu, Xiaosheng He, Jun Yu, Hongbing Shen, Dong Hang
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引用次数: 0

摘要

代谢紊乱在结直肠癌(CRC)的发生中起着至关重要的作用,但对早期发现结直肠癌及其前驱病变有用的代谢物的鉴定仍然难以捉摸。我们在一项两阶段病例对照研究中采用液相色谱-质谱法进行了非靶向血浆代谢组学分析,其中包括219例结直肠癌病例、164例结直肠癌腺瘤(CRA)病例和219例正常对照(NC)作为训练集,91例结直肠癌、115例结直肠癌和109例NC作为验证集。在891个已命名的代谢物中,239个在CRC与NC中显著改变,26个在CRA与NC中显著改变,88个在CRC与CRA中显著改变。在调整潜在混杂因素后,结果是稳定的。10种代谢物,包括6种脂类、1种苯类、1种有机杂环化合物、1种有机酸衍生物和1种有机氧化合物,在鉴别CRC和NC方面表现最佳(AUC = 0.81)。此外,7种代谢物在区分CRA和NC方面表现最佳,AUC为0.89。我们的研究结果提供了新的证据,支持特定的血浆代谢物,特别是那些与脂质代谢有关的代谢物,作为CRC早期检测的有希望的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery and Validation of Novel Biomarkers for Colorectal Neoplasia Detection via Plasma Metabolomics

Metabolic disturbance plays a critical role in the initiation of colorectal cancer (CRC), yet the identification of metabolites that are useful for early detection of CRC and its precursor lesions remains elusive. We conducted an untargeted plasma metabolomic profiling by liquid chromatography-mass spectrometry in a two-stage case–control study, including 219 CRC cases, 164 colorectal adenoma (CRA) cases, and 219 normal controls (NC) as a training set, and 91 CRC, 115 CRA, and 109 NC as a validation set. Among 891 named metabolites, 239 were significantly altered in CRC versus NC, 26 in CRA versus NC, and 88 in CRC versus CRA within the training set. The results were stable when adjusting for potential confounders. A panel of 10 metabolites, including six lipid species, one benzenoid, one organoheterocyclic compound, one organic acid derivative, and one organic oxygen compound, showed optimal performance in discriminating CRC from NC (AUC = 0.81) in the validation. Moreover, a panel of seven metabolites exhibited optimal performance in discriminating CRA from NC, with an AUC of 0.89. Our findings provide novel evidence supporting specific plasma metabolites, particularly those implicated in lipid metabolism, as promising biomarkers for the early detection of CRC.

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来源期刊
CiteScore
6.70
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