Literature DB >> 31511427

Machine learning analysis of DNA methylation profiles distinguishes primary lung squamous cell carcinomas from head and neck metastases.

Philipp Jurmeister1,2,3, Michael Bockmayr1,4,5, Philipp Seegerer6, Teresa Bockmayr1, Denise Treue1, Grégoire Montavon6, Claudia Vollbrecht1,3,7, Alexander Arnold1, Daniel Teichmann8, Keno Bressem9, Ulrich Schüller4,5,10, Maximilian von Laffert1, Klaus-Robert Müller6,11,12, David Capper13,8, Frederick Klauschen14,3.   

Abstract

Head and neck squamous cell carcinoma (HNSC) patients are at risk of suffering from both pulmonary metastases or a second squamous cell carcinoma of the lung (LUSC). Differentiating pulmonary metastases from primary lung cancers is of high clinical importance, but not possible in most cases with current diagnostics. To address this, we performed DNA methylation profiling of primary tumors and trained three different machine learning methods to distinguish metastatic HNSC from primary LUSC. We developed an artificial neural network that correctly classified 96.4% of the cases in a validation cohort of 279 patients with HNSC and LUSC as well as normal lung controls, outperforming support vector machines (95.7%) and random forests (87.8%). Prediction accuracies of more than 99% were achieved for 92.1% (neural network), 90% (support vector machine), and 43% (random forest) of these cases by applying thresholds to the resulting probability scores and excluding samples with low confidence. As independent clinical validation of the approach, we analyzed a series of 51 patients with a history of HNSC and a second lung tumor, demonstrating the correct classifications based on clinicopathological properties. In summary, our approach may facilitate the reliable diagnostic differentiation of pulmonary metastases of HNSC from primary LUSC to guide therapeutic decisions.
Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2019        PMID: 31511427     DOI: 10.1126/scitranslmed.aaw8513

Source DB:  PubMed          Journal:  Sci Transl Med        ISSN: 1946-6234            Impact factor:   17.956


  34 in total

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3.  Clinical epigenomics for cardiovascular disease: Diagnostics and therapies.

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4.  Ultrasensitive detection of circulating tumour DNA via deep methylation sequencing aided by machine learning.

Authors:  Naixin Liang; Bingsi Li; Ziqi Jia; Chenyang Wang; Pancheng Wu; Tao Zheng; Yanyu Wang; Fujun Qiu; Yijun Wu; Jing Su; Jiayue Xu; Feng Xu; Huiling Chu; Shuai Fang; Xingyu Yang; Chengju Wu; Zhili Cao; Lei Cao; Zhongxing Bing; Hongsheng Liu; Li Li; Cheng Huang; Yingzhi Qin; Yushang Cui; Han Han-Zhang; Jianxing Xiang; Hao Liu; Xin Guo; Shanqing Li; Heng Zhao; Zhihong Zhang
Journal:  Nat Biomed Eng       Date:  2021-06-15       Impact factor: 25.671

Review 5.  The regulation mechanisms and the Lamarckian inheritance property of DNA methylation in animals.

Authors:  Yulong Li; Yujing Xu; Tongxu Liu; Hengyi Chang; Xiaojun Yang
Journal:  Mamm Genome       Date:  2021-04-15       Impact factor: 2.957

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7.  Identification of the origin of brain metastases based on the relative methylation orderings of CpG sites.

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10.  DIMEimmune: Robust estimation of infiltrating lymphocytes in CNS tumors from DNA methylation profiles.

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