4.7 Article

Pharmaco-miR: linking microRNAs and drug effects

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 15, Issue 4, Pages 648-659

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbs082

Keywords

microRNAs; pharmacogenomics; database; web server; miRNA pharmacogenomic set; Pharmaco-miR

Funding

  1. Memorial Foundation of Eva and Henry Fraenkel
  2. Harboe Foundation
  3. Aase and Einar Danielsen Foundation
  4. Danish Council for Strategic Research
  5. Edmond J. Safra Center for Bioinformatics at Tel Aviv University
  6. Chief Scientist Office, Ministry of Health, Israel [3-4876]
  7. Israel Cancer Association
  8. Wolfson family Charitable Fund
  9. I-CORE Program of the Planning and Budgeting Committee
  10. Israel Science Foundation [41/11]

Ask authors/readers for more resources

MicroRNAs (miRNAs) are short regulatory RNAs that down-regulate gene expression. They are essential for cell homeostasis and active in many disease states. A major discovery is the ability of miRNAs to determine the efficacy of drugs, which has given rise to the field of 'miRNA pharmacogenomics' through 'Pharmaco-miRs'. miRNAs play a significant role in pharmacogenomics by down-regulating genes that are important for drug function. These interactions can be described as triplet sets consisting of a miRNA, a target gene and a drug associated with the gene. We have developed a web server which links miRNA expression and drug function by combining data on miRNA targeting and protein-drug interactions. miRNA targeting information derive from both experimental data and computational predictions, and protein-drug interactions are annotated by the Pharmacogenomics Knowledge base (PharmGKB). Pharmaco-miR's input consists of miRNAs, genes and/or drug names and the output consists of miRNA pharmacogenomic sets or a list of unique associated miRNAs, genes and drugs. We have furthermore built a database, named Pharmaco-miR Verified Sets (VerSe), which contains miRNA pharmacogenomic data manually curated from the literature, can be searched and downloaded via Pharmaco-miR and informs on trends and generalities published in the field. Overall, we present examples of how Pharmaco-miR provides possible explanations for previously published observations, including how the cisplatin and 5-fluorouracil resistance induced by miR-148a may be caused by miR-148a targeting of the gene KIT. The information is available at www.Pharmaco-miR.org.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available