Transcriptomic Module Discovery of Diarrhea-Predominant Irritable Bowel Syndrome: A Causal Network Inference Approach

被引:0
作者
Guido, Davide [1 ]
Maqoud, Fatima [2 ]
Aloisio, Michelangelo [2 ]
Mallardi, Domenica [2 ]
Ura, Blendi [3 ]
Gualandi, Nicolo [4 ]
Cocca, Massimiliano [5 ,6 ]
Russo, Francesco [2 ]
机构
[1] Natl Inst Gastroenterol, Data Sci Unit, IRCCS Saverio Bellis, I-70013 Castellana Grotte, Italy
[2] IRCCS Saverio de Bellis, Funct Gastrointestinal Disorders Res Grp, Natl Inst Gastroenterol, I-70013 Castellana Grotte, Bari, Italy
[3] IRCCS Burlo Garofolo, Inst Maternal & Child Hlth, I-34137 Trieste, Italy
[4] Univ Udine, Dept Med, Lab Biochem, Ple Kolbe 4, I-33100 Udine, Italy
[5] Canc Res Ctr Lyon CRCL, INSERM U1052, CNRS UMR 5286, F-69008 Lyon, France
[6] Inst Hepatol Lyon IHL, F-69002 Lyon, France
关键词
IBS-D; transcriptomics; causal network inference; biomarkers; therapeutic targets; EPIGENETIC INACTIVATION; COMPLEMENT-SYSTEM; GENE-EXPRESSION; DISEASE; DISORDERS; CHILDREN; CRITERIA; CELLS;
D O I
10.3390/ijms25179322
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Irritable bowel syndrome with diarrhea (IBS-D) is the most prevalent subtype of IBS, characterized by chronic gastrointestinal symptoms in the absence of identifiable pathological findings. This study aims to investigate the molecular mechanisms underlying IBS-D using transcriptomic data. By employing causal network inference methods, we identify key transcriptomic modules associated with IBS-D. Utilizing data from public databases and applying advanced computational techniques, we uncover potential biomarkers and therapeutic targets. Our analysis reveals significant molecular alterations that affect cellular functions, offering new insights into the complex pathophysiology of IBS-D. These findings enhance our understanding of the disease and may foster the development of more effective treatments.
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页数:24
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