Evidence map›Paper›PMID 24627819›Full record

ArticleHealthcare informatics research2014

Drug similarity search based on combined signatures in gene expression profiles.

Kihoon Cha, Min-Sung Kim, Kimin Oh, Hyunjung Shin, Gwan-Su Yi

Erratum issuedAbstract read
In one paragraph

Article in Healthcare informatics research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Computing Drug-Drug Similarity from Patient-Centric Data.Bioengineering (Basel, Switzerland) · 2023
    Article
  3. Article
  4. Article
  5. Article
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors.

Kihoon ChaDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Min-Sung KimDepartment of Information and Communications Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Kimin OhDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Hyunjung ShinDepartment of Industrial Engineering, Ajou University, Suwon, Korea.
Gwan-Su YiDepartment of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesRecently, comparison of drug responses on gene expression has been a major approach to identifying the functional similarity of drugs. Previous studies have mostly focused on a single feature, the expression differences of individual genes. We provide a more robust and accurate method to compare the functional similarity of drugs by diversifying the features of comparison in gene expression and considering the sample dependent variations.

methodsFor differentially expressed gene measurement, we modified the conventional t-test to normalize variations in diverse experimental conditions of individual samples. To extract significant differentially co-expressed gene modules, we searched maximal cliques among the co-expressed gene network. Finally, we calculated a combined similarity score by averaging the two scaled scores from the above two measurements.

resultsThis method shows significant performance improvement in comparison to other approaches in the test with Connectivity Map data. In the test to find the drugs based on their own expression profiles with leave-one-out cross validation, the proposed method showed an area under the curve (AUC) score of 0.99, which is much higher than scores obtained with previous methods, ranging from 0.71 to 0.93. In the drug networks, we could find well clustered drugs having the same target proteins and novel relations among drugs implying the possibility of drug repurposing.

conclusionsInclusion of the features of a co-expressed module provides more implications to infer drug action. We propose that this method be used to find collaborative cellular mechanisms associated with drug action and to simply identify drugs having similar responses.

Indexed as

Drug RepositioningGene Expression RegulationGene Regulatory NetworksPharmacological BiomarkersTranscriptome

Identifiers

PMID24627819
PMCPMC3950266

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.