Drug Discovery: Genomic and Transcriptomic Approaches

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Biopharmaceuticals".

Deadline for manuscript submissions: closed (31 May 2023) | Viewed by 2391

Special Issue Editor


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Guest Editor
Department of Neurology, Jinan University, Guangzhou, China
Interests: bioinformatics; omics; drug discovery

Special Issue Information

Dear Colleagues,

With the development of sequencing capability and bioinformatics analytic tools, omics have become an indispensable tool in modern drug discovery. High-throughput data such as genomic, epigenetic, transcriptomic, proteomic, metabolomic, and ribosome profiling data as well as single-cell sequencing have all made significant contributions to mechanism-based drug discovery and drug repurposing. Omics data analysis can not only accelerate drug target identification and drug candidate screening but can also facilitate the characterization of side effects and predict drug resistance.

For this Special Issue, we encourage the use of omics data for drug-discovery-related exploration, aiming to provide a forum for advances in the development and application of omics-based drug-discovery strategies.

Original research articles and reviews that focus on, but are not limited to, the following topics are welcome:

  • The identification or verification of drug targets and biomarkers by integrating diverse omics data;
  • The identification of disease-associated screenable phenotypes based on omics data analysis;
  • The prediction or refinement of drug candidates through omics data mining;
  • Assessment of the potential for drug resistance or adverse drug reactions using omics data;
  • Prediction of a drug's activity, toxicity, or mechanism of action through omics data analysis. 

Prof. Dr. Keshen Li
Guest Editor

Manuscript Submission Information

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Keywords

  • omics
  • bioinformatics
  • drug discovery
  • drug response
  • drug target

Published Papers (1 paper)

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Research

19 pages, 10547 KiB  
Article
Repurposing Approved Drugs for Sarcopenia Based on Transcriptomics Data in Humans
by Shuang Liang, Danyang Liu, Zhengwu Xiao, Jonathan Greenbaum, Hui Shen, Hongmei Xiao and Hongwen Deng
Pharmaceuticals 2023, 16(4), 607; https://doi.org/10.3390/ph16040607 - 18 Apr 2023
Cited by 2 | Viewed by 2075
Abstract
Sarcopenia, characterized by age-related loss of muscle mass, strength, and decreased physical performance, is a growing public health challenge amid the rapidly ageing population. As there are no approved drugs that target sarcopenia, it has become increasingly urgent to identify promising pharmacological interventions. [...] Read more.
Sarcopenia, characterized by age-related loss of muscle mass, strength, and decreased physical performance, is a growing public health challenge amid the rapidly ageing population. As there are no approved drugs that target sarcopenia, it has become increasingly urgent to identify promising pharmacological interventions. In this study, we conducted an integrative drug repurposing analysis utilizing three distinct approaches. Firstly, we analyzed skeletal muscle transcriptomic sequencing data in humans and mice using gene differential expression analysis, weighted gene co-expression analysis, and gene set enrichment analysis. Subsequently, we employed gene expression profile similarity assessment, hub gene expression reversal, and disease-related pathway enrichment to identify and repurpose candidate drugs, followed by the integration of findings with rank aggregation algorithms. Vorinostat, the top-ranking drug, was also validated in an in vitro study, which demonstrated its efficacy in promoting muscle fiber formation. Although still requiring further validation in animal models and human clinical trials, these results suggest a promising drug repurposing prospect in the treatment and prevention of sarcopenia. Full article
(This article belongs to the Special Issue Drug Discovery: Genomic and Transcriptomic Approaches)
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