Ning Xie, Dehua Liao, Binliang Liu, Jiwen Zhang, Liping Liu, Gang Huang, Quchang Ouyang
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Ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry was utilized to analyze the metabolites in blood samples. A combination of univariate and multivariate statistical analyses was employed to identify these metabolites, and their biological functions were then ascertained by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Finally, machine learning algorithms were employed to screen responsive biomarkers from all differentially expressed metabolites.</p><p><strong>Results: </strong>Our finding revealed 6889 unique metabolites that were detected. Pathways like retinol metabolism, fatty acid biosynthesis, and steroid hormone biosynthesis were enriched for differentially expressed metabolites. Notably, two key metabolites associated with inetetamab response in BC were identified: FAPy-adenine and 2-Pyrocatechuic acid. There was some negative correlation between progress-free survival (PFS) and their kurtosis content.</p><p><strong>Conclusions: </strong>In summary, the identification of these two significant differential metabolites holds promise as potential biomarkers for evaluating and predicting inetetamab treatment outcomes in BC, ultimately contributing to the diagnosis of the disease and the discovery of prognostic markers.</p>","PeriodicalId":15509,"journal":{"name":"Journal of Clinical Laboratory Analysis","volume":" ","pages":"e25124"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interpretable Machine Learning Algorithms Identify Inetetamab-Mediated Metabolic Signatures and Biomarkers in Treating Breast Cancer.\",\"authors\":\"Ning Xie, Dehua Liao, Binliang Liu, Jiwen Zhang, Liping Liu, Gang Huang, Quchang Ouyang\",\"doi\":\"10.1002/jcla.25124\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>HER2-positive breast cancer (BC), a highly aggressive malignancy, has been treated with the targeted therapy inetetamab for metastatic cases. 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引用次数: 0
摘要
背景:HER2 阳性乳腺癌(BCHER2阳性乳腺癌(BC)是一种侵袭性极强的恶性肿瘤,目前已对转移性病例使用靶向疗法伊尼他单抗进行治疗。伊尼他单抗(Cipterbin)是最近获批的一种治疗HER2阳性转移性乳腺癌的靶向疗法,可显著延长患者的生存期。目前,还没有可靠的生物标志物来预测或评估伊尼他单抗对BC患者的疗效:方法:本研究利用代谢组学和机器学习的力量,揭示了伊美他单抗在BC治疗中的生物标志物。共收集了23份伊美他单抗治疗的BC患者的血浆样本,并将其分为应答者和非应答者。利用超高效液相色谱-四极杆飞行时间质谱分析血液样本中的代谢物。然后,通过基因本体(GO)和京都基因组百科全书(KEGG)富集分析确定了这些代谢物的生物功能。最后,采用机器学习算法从所有差异表达的代谢物中筛选出反应性生物标记物:结果:我们的研究发现,共检测到 6889 个独特的代谢物。视黄醇代谢、脂肪酸生物合成和类固醇激素生物合成等途径富含差异表达的代谢物。值得注意的是,有两种关键代谢物与乙酰替他滨对 BC 的反应有关:FAPy-腺嘌呤和2-儿茶酸。无进展生存期(PFS)与这两个代谢物的峰度含量呈负相关:总之,这两种重要的差异代谢物的鉴定有望成为评估和预测伊美他滨治疗结果的潜在生物标志物,最终有助于疾病的诊断和预后标志物的发现。
Interpretable Machine Learning Algorithms Identify Inetetamab-Mediated Metabolic Signatures and Biomarkers in Treating Breast Cancer.
Background: HER2-positive breast cancer (BC), a highly aggressive malignancy, has been treated with the targeted therapy inetetamab for metastatic cases. Inetetamab (Cipterbin) is a recently approved targeted therapy for HER2-positive metastatic BC, significantly prolonging patients' survival. Currently, there is no established biomarker to reliably predict or assess the therapeutic efficacy of inetetamab in BC patients.
Methods: This study harnesses the power of metabolomics and machine learning to uncover biomarkers for inetetamab in BC therapy. A total of 23 plasma samples from inetetamab-treated BC patients were collected and stratified into responders and nonresponders. Ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry was utilized to analyze the metabolites in blood samples. A combination of univariate and multivariate statistical analyses was employed to identify these metabolites, and their biological functions were then ascertained by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Finally, machine learning algorithms were employed to screen responsive biomarkers from all differentially expressed metabolites.
Results: Our finding revealed 6889 unique metabolites that were detected. Pathways like retinol metabolism, fatty acid biosynthesis, and steroid hormone biosynthesis were enriched for differentially expressed metabolites. Notably, two key metabolites associated with inetetamab response in BC were identified: FAPy-adenine and 2-Pyrocatechuic acid. There was some negative correlation between progress-free survival (PFS) and their kurtosis content.
Conclusions: In summary, the identification of these two significant differential metabolites holds promise as potential biomarkers for evaluating and predicting inetetamab treatment outcomes in BC, ultimately contributing to the diagnosis of the disease and the discovery of prognostic markers.
期刊介绍:
Journal of Clinical Laboratory Analysis publishes original articles on newly developing modes of technology and laboratory assays, with emphasis on their application in current and future clinical laboratory testing. This includes reports from the following fields: immunochemistry and toxicology, hematology and hematopathology, immunopathology, molecular diagnostics, microbiology, genetic testing, immunohematology, and clinical chemistry.