Pharmaco-miR: linking microRNAs and drug effects

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Pharmaco-miR : linking microRNAs and drug effects. / Rukov, Jakob Lewin; Wilentzik, Roni; Jaffe, Ishai; Vinther, Jeppe; Shomron, Noam.

In: Briefings in Bioinformatics, Vol. 15, No. 4, 2014, p. 648-659.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rukov, JL, Wilentzik, R, Jaffe, I, Vinther, J & Shomron, N 2014, 'Pharmaco-miR: linking microRNAs and drug effects', Briefings in Bioinformatics, vol. 15, no. 4, pp. 648-659. https://doi.org/10.1093/bib/bbs082

APA

Rukov, J. L., Wilentzik, R., Jaffe, I., Vinther, J., & Shomron, N. (2014). Pharmaco-miR: linking microRNAs and drug effects. Briefings in Bioinformatics, 15(4), 648-659. https://doi.org/10.1093/bib/bbs082

Vancouver

Rukov JL, Wilentzik R, Jaffe I, Vinther J, Shomron N. Pharmaco-miR: linking microRNAs and drug effects. Briefings in Bioinformatics. 2014;15(4):648-659. https://doi.org/10.1093/bib/bbs082

Author

Rukov, Jakob Lewin ; Wilentzik, Roni ; Jaffe, Ishai ; Vinther, Jeppe ; Shomron, Noam. / Pharmaco-miR : linking microRNAs and drug effects. In: Briefings in Bioinformatics. 2014 ; Vol. 15, No. 4. pp. 648-659.

Bibtex

@article{1f8c9daf431844648df3d796bf281649,
title = "Pharmaco-miR: linking microRNAs and drug effects",
abstract = "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.",
author = "Rukov, {Jakob Lewin} and Roni Wilentzik and Ishai Jaffe and Jeppe Vinther and Noam Shomron",
year = "2014",
doi = "10.1093/bib/bbs082",
language = "English",
volume = "15",
pages = "648--659",
journal = "Briefings in Bioinformatics",
issn = "1467-5463",
publisher = "Oxford University Press",
number = "4",

}

RIS

TY - JOUR

T1 - Pharmaco-miR

T2 - linking microRNAs and drug effects

AU - Rukov, Jakob Lewin

AU - Wilentzik, Roni

AU - Jaffe, Ishai

AU - Vinther, Jeppe

AU - Shomron, Noam

PY - 2014

Y1 - 2014

N2 - 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.

AB - 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.

U2 - 10.1093/bib/bbs082

DO - 10.1093/bib/bbs082

M3 - Journal article

C2 - 23376192

VL - 15

SP - 648

EP - 659

JO - Briefings in Bioinformatics

JF - Briefings in Bioinformatics

SN - 1467-5463

IS - 4

ER -

ID: 44741846