Evidence map›Paper›PMID 28198666›Full record

ArticleBMC genomics2017

DeSigN: connecting gene expression with therapeutics for drug repurposing and development.

Bernard Kok Bang Lee, Kai Hung Tiong, Jit Kang Chang, Chee Sun Liew, Zainal Ariff Abdul Rahman, Aik Choon Tan, Tsung Fei Khang, Sok Ching Cheong

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
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  3. Review
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  7. Article
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  9. Article
  10. Computational Methods for Drug Repurposing.Advances in experimental medicine and biology · 2022
    Article
  11. Article
  12. Article
  13. Diagnostic and prognostic value of thymidylate synthase expression in breast cancer.Clinical and experimental pharmacology & physiology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Time-Course Transcriptome Analysis for Drug Repositioning inFrontiers in cell and developmental biology · 2019
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Bernard Kok Bang LeeDepartment of Oral & Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Kai Hung TiongDepartment of Oral & Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Jit Kang ChangData Intensive Computing Centre, Research Management & Innovation Complex, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Chee Sun LiewData Intensive Computing Centre, Research Management & Innovation Complex, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Zainal Ariff Abdul RahmanDepartment of Oral & Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Aik Choon TanDivision of Medical Oncology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.
Tsung Fei KhangCentre for Data Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Sok Ching CheongDepartment of Oral & Maxillofacial Clinical Sciences, Faculty of Dentistry, University of Malaya, 50603, Kuala Lumpur, Malaysia. sokching.cheong@cancerresearch.my.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe drug discovery and development pipeline is a long and arduous process that inevitably hampers rapid drug development. Therefore, strategies to improve the efficiency of drug development are urgently needed to enable effective drugs to enter the clinic. Precision medicine has demonstrated that genetic features of cancer cells can be used for predicting drug response, and emerging evidence suggest that gene-drug connections could be predicted more accurately by exploring the cumulative effects of many genes simultaneously.

resultsWe developed DeSigN, a web-based tool for predicting drug efficacy against cancer cell lines using gene expression patterns. The algorithm correlates phenotype-specific gene signatures derived from differentially expressed genes with pre-defined gene expression profiles associated with drug response data (IC

conclusionsDeSigN is a robust method that is useful for the identification of candidate drugs using an input gene signature obtained from gene expression analysis. This user-friendly platform could be used to identify drugs with unanticipated efficacy against cancer cell lines of interest, and therefore could be used for the repurposing of drugs, thus improving the efficiency of drug development.

Indexed as

Drug DesignDrug RepositioningSoftwareAlgorithmsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationComputational BiologyDatabases, GeneticGene Expression ProfilingGene Expression RegulationHumansInhibitory Concentration 50Protein Kinase InhibitorsReproducibility of ResultsAntineoplastic AgentsProtein Kinase InhibitorsCancerCell lineDeSigNDrug repurposingGene expression

Identifiers

PMID28198666
PMCPMC5310278

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Registered trials

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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.