| Literature DB >> 33207877 |
Malena Manzi1,2, Martín Palazzo3,4, María Elena Knott1, Pierre Beauseroy3, Patricio Yankilevich4, María Isabel Giménez5, María Eugenia Monge1.
Abstract
A discovery-based lipid profiling study of serum samples from a cohort that included patients with clear cell renal cell carcinoma (ccRCC) stages I, II, III, and IV (n = 112) and controls (n = 52) was performed using ultraperformance liquid chromatography coupled to quadrupole-time-of-flight mass spectrometry and machine learning techniques. Multivariate models based on support vector machines and the LASSO variable selection method yielded two discriminant lipid panels for ccRCC detection and early diagnosis. A 16-lipid panel allowed discriminating ccRCC patients from controls with 95.7% accuracy in a training set under cross-validation and 77.1% accuracy in an independent test set. A second model trained to discriminate early (I and II) from late (III and IV) stage ccRCC yielded a panel of 26 compounds that classified stage I patients from an independent test set with 82.1% accuracy. Thirteen species, including cholic acid, undecylenic acid, lauric acid, LPC(16:0/0:0), and PC(18:2/18:2), identified with level 1 exhibited significantly lower levels in samples from ccRCC patients compared to controls. Moreover, 3α-hydroxy-5α-androstan-17-one 3-sulfate, cis-5-dodecenoic acid, arachidonic acid, cis-13-docosenoic acid, PI(16:0/18:1), PC(16:0/18:2), and PC(O-16:0/20:4) contributed to discriminate early from late ccRCC stage patients. The results are auspicious for early ccRCC diagnosis after validation of the panels in larger and different cohorts.Entities:
Keywords: LASSO; biomarkers; clear cell renal cell carcinoma; lipidomics; machine learning; mass spectrometry; support vector machines; ultraperformance liquid chromatography
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Year: 2020 PMID: 33207877 DOI: 10.1021/acs.jproteome.0c00663
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466