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Machine learning of serum metabolic patterns encodes early-stage lung adenocarcinoma

Early cancer detection greatly increases the chances for successful treatment, but available diagnostics for some tumours, including lung adenocarcinoma (LA), are limited. An ideal early-stage diagnosis of LA for large-scale clinical use must address quick detection, low invasiveness, and high perfo...

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Detalles Bibliográficos
Autores principales: Huang, Lin, Wang, Lin, Hu, Xiaomeng, Chen, Sen, Tao, Yunwen, Su, Haiyang, Yang, Jing, Xu, Wei, Vedarethinam, Vadanasundari, Wu, Shu, Liu, Bin, Wan, Xinze, Lou, Jiatao, Wang, Qian, Qian, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366718/
https://www.ncbi.nlm.nih.gov/pubmed/32678093
http://dx.doi.org/10.1038/s41467-020-17347-6
Descripción
Sumario:Early cancer detection greatly increases the chances for successful treatment, but available diagnostics for some tumours, including lung adenocarcinoma (LA), are limited. An ideal early-stage diagnosis of LA for large-scale clinical use must address quick detection, low invasiveness, and high performance. Here, we conduct machine learning of serum metabolic patterns to detect early-stage LA. We extract direct metabolic patterns by the optimized ferric particle-assisted laser desorption/ionization mass spectrometry within 1 s using only 50 nL of serum. We define a metabolic range of 100–400 Da with 143 m/z features. We diagnose early-stage LA with sensitivity~70–90% and specificity~90–93% through the sparse regression machine learning of patterns. We identify a biomarker panel of seven metabolites and relevant pathways to distinguish early-stage LA from controls (p < 0.05). Our approach advances the design of metabolic analysis for early cancer detection and holds promise as an efficient test for low-cost rollout to clinics.