Drug Repurposing - Molecular Aspects and Therapeutic Applications 2022
DOI: 10.5772/intechopen.101377
|View full text |Cite
|
Sign up to set email alerts
|

Gene Signature-Based Drug Repositioning

Abstract: With the advent of dynamical omics technology, especially the transcriptome and proteome, a huge amount of data related to various diseases and approved drugs are available under multi global projects or researches with their interests. These omics data and new machine learning technology largely promote the translation of drug research into clinical trials. We will cover the following topics in this chapter. 1) An introduction to the basic discipline of gene signature-based drug repurposing; 2) databases of g… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 84 publications
0
1
0
Order By: Relevance
“…Gene expression reversal methodology is increasingly being utilized to identify potential drugs for repurposing. 1 - 4 The underlying assumption of these approaches is that a disease can be treated by a drug that has been shown to revert the disease related gene expression signature (GES) back to a normal gene expression state. This approach has been enabled by the fast growth of large publically available gene expression databases such as GEO (Gene Expression Omnibus) at the National Center for Biotechnology Information (NCBI), 5 the large-scale perturbation database termed Connectivity Map (CMap), 6 and the Library of Integrated Network-Based Cellular Signatures (LINCS).…”
Section: Introductionmentioning
confidence: 99%
“…Gene expression reversal methodology is increasingly being utilized to identify potential drugs for repurposing. 1 - 4 The underlying assumption of these approaches is that a disease can be treated by a drug that has been shown to revert the disease related gene expression signature (GES) back to a normal gene expression state. This approach has been enabled by the fast growth of large publically available gene expression databases such as GEO (Gene Expression Omnibus) at the National Center for Biotechnology Information (NCBI), 5 the large-scale perturbation database termed Connectivity Map (CMap), 6 and the Library of Integrated Network-Based Cellular Signatures (LINCS).…”
Section: Introductionmentioning
confidence: 99%