Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies

Obesity is an excess accumulation of body fat. Its progression rate has remained high in recent years. Therefore, the aim of this study was to diagnose important differentially expressed genes (DEGs) associated in its development, which may be used as novel biomarkers or potential therapeutic target...

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Main Authors: Harish Joshi, Basavaraj Vastrad, Nidhi Joshi, Chanabasayya Vastrad, Anandkumar Tengli, Iranna Kotturshetti
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2021.628907/full
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author Harish Joshi
Basavaraj Vastrad
Nidhi Joshi
Chanabasayya Vastrad
Anandkumar Tengli
Iranna Kotturshetti
author_facet Harish Joshi
Basavaraj Vastrad
Nidhi Joshi
Chanabasayya Vastrad
Anandkumar Tengli
Iranna Kotturshetti
author_sort Harish Joshi
collection DOAJ
description Obesity is an excess accumulation of body fat. Its progression rate has remained high in recent years. Therefore, the aim of this study was to diagnose important differentially expressed genes (DEGs) associated in its development, which may be used as novel biomarkers or potential therapeutic targets for obesity. The gene expression profile of E-MTAB-6728 was downloaded from the database. After screening DEGs in each ArrayExpress dataset, we further used the robust rank aggregation method to diagnose 876 significant DEGs including 438 up regulated and 438 down regulated genes. Functional enrichment analysis was performed. These DEGs were shown to be significantly enriched in different obesity related pathways and GO functions. Then protein–protein interaction network, target genes - miRNA regulatory network and target genes - TF regulatory network were constructed and analyzed. The module analysis was performed based on the whole PPI network. We finally filtered out STAT3, CORO1C, SERPINH1, MVP, ITGB5, PCM1, SIRT1, EEF1G, PTEN and RPS2 hub genes. Hub genes were validated by ICH analysis, receiver operating curve (ROC) analysis and RT-PCR. Finally a molecular docking study was performed to find small drug molecules. The robust DEGs linked with the development of obesity were screened through the expression profile, and integrated bioinformatics analysis was conducted. Our study provides reliable molecular biomarkers for screening and diagnosis, prognosis as well as novel therapeutic targets for obesity.
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spelling doaj.art-5ba79dbba099469daab322be70401b7a2022-12-21T20:26:21ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922021-06-011210.3389/fendo.2021.628907628907Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking StudiesHarish Joshi0Basavaraj Vastrad1Nidhi Joshi2Chanabasayya Vastrad3Anandkumar Tengli4Iranna Kotturshetti5Department of Endocrinology, Endocrine and Diabetes Care Center, Hubbali, IndiaDepartment of Biochemistry, Basaveshwar College of Pharmacy, Gadag, IndiaDepartment of Medicine, Dr. D. Y. Patil Medical College, Kolhapur, IndiaBiostatistics and Bioinformatics, Chanabasava Nilaya, Bharthinagar, Dharwad, IndiaDepartment of Pharmaceutical Chemistry, JSS College of Pharmacy, Mysuru and JSS Academy of Higher Education & Research, Mysuru, IndiaDepartment of Ayurveda, Rajiv Gandhi Education Society`s Ayurvedic Medical College, Ron, IndiaObesity is an excess accumulation of body fat. Its progression rate has remained high in recent years. Therefore, the aim of this study was to diagnose important differentially expressed genes (DEGs) associated in its development, which may be used as novel biomarkers or potential therapeutic targets for obesity. The gene expression profile of E-MTAB-6728 was downloaded from the database. After screening DEGs in each ArrayExpress dataset, we further used the robust rank aggregation method to diagnose 876 significant DEGs including 438 up regulated and 438 down regulated genes. Functional enrichment analysis was performed. These DEGs were shown to be significantly enriched in different obesity related pathways and GO functions. Then protein–protein interaction network, target genes - miRNA regulatory network and target genes - TF regulatory network were constructed and analyzed. The module analysis was performed based on the whole PPI network. We finally filtered out STAT3, CORO1C, SERPINH1, MVP, ITGB5, PCM1, SIRT1, EEF1G, PTEN and RPS2 hub genes. Hub genes were validated by ICH analysis, receiver operating curve (ROC) analysis and RT-PCR. Finally a molecular docking study was performed to find small drug molecules. The robust DEGs linked with the development of obesity were screened through the expression profile, and integrated bioinformatics analysis was conducted. Our study provides reliable molecular biomarkers for screening and diagnosis, prognosis as well as novel therapeutic targets for obesity.https://www.frontiersin.org/articles/10.3389/fendo.2021.628907/fulladipositiesobesitydifferentially expressed genesmodulesprotein–protein interaction network
spellingShingle Harish Joshi
Basavaraj Vastrad
Nidhi Joshi
Chanabasayya Vastrad
Anandkumar Tengli
Iranna Kotturshetti
Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies
Frontiers in Endocrinology
adiposities
obesity
differentially expressed genes
modules
protein–protein interaction network
title Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies
title_full Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies
title_fullStr Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies
title_full_unstemmed Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies
title_short Identification of Key Pathways and Genes in Obesity Using Bioinformatics Analysis and Molecular Docking Studies
title_sort identification of key pathways and genes in obesity using bioinformatics analysis and molecular docking studies
topic adiposities
obesity
differentially expressed genes
modules
protein–protein interaction network
url https://www.frontiersin.org/articles/10.3389/fendo.2021.628907/full
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