Obesity-related Drug-Gene Interaction Analysis Service
InquiryObesity-related drug-gene interaction analysis is a crucial method for understanding how genetic factors influence drug responses in obese patients, particularly concerning treatment strategies that target obesity-related conditions. At Protheragen, our service for obesity-related drug-gene interaction analysis integrates bioinformatics and network pharmacology to analyze key genes and signaling pathways involved in obesity and related metabolic disorders.
Unlock the Genetic Code to Personalized Obesity Treatment with Our Drug-Gene Interaction Analysis
The obesity-related drug-gene interaction analysis service at Protheragen focuses on identifying differentially expressed genes (DEGs) associated with obesity, particularly those involved in lipid metabolism, insulin resistance, and inflammation. By leveraging bioinformatics tools and mining public databases like GEO and FerrDb, our service constructs comprehensive networks of drug-gene interactions, including transcription factors and miRNAs. Key genes such as IL-6, VEGFA, PTGS2, and STAT3 are integrated into protein-protein interaction (PPI) networks using Cytoscape to highlight potential therapeutic targets. Additionally, the analysis explores the interplay between the immune system and metabolism, identifying immune cells like macrophages and T cells that influence drug responses, aiming to reduce inflammation associated with obesity.
Our team utilizes data mining tools to extract gene and drug interaction information from public databases, constructing drug-gene interaction networks. With the help of tools, key genes are integrated into protein-protein interaction networks, further revealing obesity-related signaling pathways and potential drug targets.
Data Acquisition
Gene expression data from public repositories like GEO and databases such as FerrDb are collected. For example, datasets like GSE2508 and GSE25401 provide human adipose tissue gene profiles.
Differential Gene Expression Analysis
Using tools like the 'limma' package in R, DEGs are identified by comparing obese and non-obese samples. This analysis filters genes based on fold-change and p-values, narrowing down those relevant to obesity.
Network Construction
PPI networks are created using the STRING database, highlighting key genes linked to obesity-related pathways, which are further analyzed for drug-gene interactions using Cytoscape.
Drug Interaction Prediction
Using databases such as DGIdb, candidate drugs that can potentially target the identified key genes are predicted. Examples of such drugs include statins and anti-inflammatory agents targeting IL-6 and other critical markers.
Anti-Obesity Therapy Development
We also provide a full range of services to facilitate the development of anti-obesity therapies and conduct in-depth preclinical studies using a wealth of cell and animal models.
Applications
- This service can be used to identify gene-drug interactions in obese individuals, allowing for tailored treatment strategies that optimize therapeutic efficacy.
- This service can be used to assist pharmaceutical companies in identifying genetic markers that influence drug response, facilitating the development of more effective obesity treatments.
- This service reveals genetic pathways involved in obesity, providing deeper insights into the disease's underlying mechanisms and potential intervention points.
- This service helps in determining how multiple drugs interact with specific genetic factors, guiding combination therapies to treat obesity and related comorbidities.
Advantages
- Our service enables precise therapeutic approaches by identifying how specific genes affect drug metabolism and efficacy in obese patients.
- Our service utilizes bioinformatics tools to integrate large datasets from public databases, providing a robust analysis of genetic and drug interactions.
- By identifying gene variations that influence drug response, our service helps improve the success rates of obesity treatments.
- This service reduces the time and expense associated with trial-and-error approaches in drug development and research by offering targeted genetic insights.
Publication
Technology: PharmMapper, SwissTargetPrediction, PPI, Cytoscape, ClusterProfiler, AutoDock
Journal: Frontiers in Endocrinology
IF: 3.9
Published: 2020
Results: This study explores the therapeutic potential of melatonin in treating leptin resistance-induced obesity using a network pharmacology approach. By identifying 33 common targets between melatonin and LR-induced obesity, including key hub genes like TP53, AKT1, and TNF, the study highlights melatonin's impact on critical pathways such as lipid metabolism, inflammation, and endocrine resistance. Through bioinformatic analyses and molecular docking, the research demonstrates melatonin's ability to bind strongly to obesity-related proteins, suggesting its role in reducing obesity-related complications by modulating metabolic and inflammatory pathways.
Fig.1 PPI network of LR-induced obesity. (Suriagandhi & Nachiappan, 2020)
Frequently Asked Questions
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What kind of data is used in this analysis?
The service utilizes gene expression data, drug-gene interaction databases, protein-protein interaction networks, and public resources like GEO and FerrDb for comprehensive analysis.
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Can this analysis predict adverse drug reactions?
Yes, the service can help predict potential adverse drug reactions by identifying gene variants that affect drug metabolism and response in obese patients.
At Protheragen, our obesity-related drug-gene interaction analysis service provides a cutting-edge approach to understanding how genetic factors influence drug responses in obesity. Please feel free to contact us to learn more about our services and innovative anti-obesity solutions.
Reference
- Suriagandhi, V.; Nachiappan V. Therapeutic target analysis and molecular mechanism of melatonin-treated leptin resistance induced obesity: A systematic study of network pharmacology. Frontiers in Endocrinology. 2020, 13: 927576. (CC BY 4.0)
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.