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Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers

Systemic Sclerosis (SSc) is an autoimmune disease associated with changes in the skin's structure in which the immune system attacks the body. A recent meta-analysis has reported a high incidence of cancer prognosis including lung cancer (LC), leukemia (LK), and lymphoma (LP) in patients with S...

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Autores principales: Islam, Md Khairul, Rahman, Md. Habibur, Islam, Md Rakibul, Islam, Md Zahidul, Mamun, Md Mainul Islam, Azad, A.K.M., Moni, Mohammad Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841363/
https://www.ncbi.nlm.nih.gov/pubmed/35198765
http://dx.doi.org/10.1016/j.heliyon.2022.e08892
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author Islam, Md Khairul
Rahman, Md. Habibur
Islam, Md Rakibul
Islam, Md Zahidul
Mamun, Md Mainul Islam
Azad, A.K.M.
Moni, Mohammad Ali
author_facet Islam, Md Khairul
Rahman, Md. Habibur
Islam, Md Rakibul
Islam, Md Zahidul
Mamun, Md Mainul Islam
Azad, A.K.M.
Moni, Mohammad Ali
author_sort Islam, Md Khairul
collection PubMed
description Systemic Sclerosis (SSc) is an autoimmune disease associated with changes in the skin's structure in which the immune system attacks the body. A recent meta-analysis has reported a high incidence of cancer prognosis including lung cancer (LC), leukemia (LK), and lymphoma (LP) in patients with SSc as comorbidity but its underlying mechanistic details are yet to be revealed. To address this research gap, bioinformatics methodologies were developed to explore the comorbidity interactions between a pair of diseases. Firstly, appropriate gene expression datasets from different repositories on SSc and its comorbidities were collected. Then the interconnection between SSc and its cancer comorbidities was identified by applying the developed pipelines. The pipeline was designed as a generic workflow to demonstrate a premise comorbid condition that integrate regarding gene expression data, tissue/organ meta-data, Gene Ontology (GO), Molecular pathways, and other online resources, and analyze them with Gene Set Enrichment Analysis (GSEA), Pathway enrichment and Semantic Similarity (SS). The pipeline was implemented in R and can be accessed through our Github repository: https://github.com/hiddenntreasure/comorbidity. Our result suggests that SSc and its cancer comorbidities share differentially expressed genes, functional terms (gene ontology), and pathways. The findings have led to a better understanding of disease pathways and our developed methodologies may be applied to any set of diseases for finding any association between them. This research may be used by physicians, researchers, biologists, and others.
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spelling pubmed-88413632022-02-22 Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers Islam, Md Khairul Rahman, Md. Habibur Islam, Md Rakibul Islam, Md Zahidul Mamun, Md Mainul Islam Azad, A.K.M. Moni, Mohammad Ali Heliyon Research Article Systemic Sclerosis (SSc) is an autoimmune disease associated with changes in the skin's structure in which the immune system attacks the body. A recent meta-analysis has reported a high incidence of cancer prognosis including lung cancer (LC), leukemia (LK), and lymphoma (LP) in patients with SSc as comorbidity but its underlying mechanistic details are yet to be revealed. To address this research gap, bioinformatics methodologies were developed to explore the comorbidity interactions between a pair of diseases. Firstly, appropriate gene expression datasets from different repositories on SSc and its comorbidities were collected. Then the interconnection between SSc and its cancer comorbidities was identified by applying the developed pipelines. The pipeline was designed as a generic workflow to demonstrate a premise comorbid condition that integrate regarding gene expression data, tissue/organ meta-data, Gene Ontology (GO), Molecular pathways, and other online resources, and analyze them with Gene Set Enrichment Analysis (GSEA), Pathway enrichment and Semantic Similarity (SS). The pipeline was implemented in R and can be accessed through our Github repository: https://github.com/hiddenntreasure/comorbidity. Our result suggests that SSc and its cancer comorbidities share differentially expressed genes, functional terms (gene ontology), and pathways. The findings have led to a better understanding of disease pathways and our developed methodologies may be applied to any set of diseases for finding any association between them. This research may be used by physicians, researchers, biologists, and others. Elsevier 2022-02-08 /pmc/articles/PMC8841363/ /pubmed/35198765 http://dx.doi.org/10.1016/j.heliyon.2022.e08892 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Islam, Md Khairul
Rahman, Md. Habibur
Islam, Md Rakibul
Islam, Md Zahidul
Mamun, Md Mainul Islam
Azad, A.K.M.
Moni, Mohammad Ali
Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers
title Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers
title_full Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers
title_fullStr Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers
title_full_unstemmed Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers
title_short Network based systems biology approach to identify diseasome and comorbidity associations of Systemic Sclerosis with cancers
title_sort network based systems biology approach to identify diseasome and comorbidity associations of systemic sclerosis with cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8841363/
https://www.ncbi.nlm.nih.gov/pubmed/35198765
http://dx.doi.org/10.1016/j.heliyon.2022.e08892
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