Unveiling new disease, pathway, and gene associations via multi-scale neural network

被引:13
|
作者
Gaudelet, Thomas [1 ]
Malod-Dognin, Noel [2 ]
Sanchez-Valle, Jon [2 ]
Pancaldi, Vera [2 ,3 ,4 ]
Valencia, Alfonso [2 ,5 ]
Przulj, Nataga [1 ,2 ,5 ]
机构
[1] UCL, Dept Comp Sci, London, England
[2] Barcelona Supercomp Ctr BSC, Barcelona, Spain
[3] Ctr Rech Cancerol Toulouse CRCT, ERL5294 CNRS, UMR1037 Inserm, F-31037 Toulouse, France
[4] Univ Paul Sabatier III, Toulouse, France
[5] ICREA, Pg Lluis Co, Barcelona, Spain
来源
PLOS ONE | 2020年 / 15卷 / 04期
基金
欧洲研究理事会;
关键词
OSTEOSARCOMA; COMORBIDITY; EXPRESSION; SYSTEM; CELLS; TUMOR; SIRT3;
D O I
10.1371/journal.pone.0231059
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Diseases involve complex modifications to the cellular machinery. The gene expression profile of the affected cells contains characteristic patterns linked to a disease. Hence, new biological knowledge about a disease can be extracted from these profiles, improving our ability to diagnose and assess disease risks. This knowledge can be used for drug re-purposing, or by physicians to evaluate a patient's condition and co-morbidity risk. Here, we consider differential gene expressions obtained by microarray technology for patients diagnosed with various diseases. Based on these data and cellular multi-scale organization, we aim at uncovering diseasedisease, disease-gene and disease-pathway associations. We propose a neural network with structure based on the multi-scale organization of proteins in a cell into biological pathways. We show that this model is able to correctly predict the diagnosis for the majority of patients. Through the analysis of the trained model, we predict disease-disease, disease-pathway, and disease-gene associations and validate the predictions by comparisons to known interactions and literature search, proposing putative explanations for the predictions.
引用
收藏
页数:12
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