Evidence map›Paper›PMID 25296724›Full record

ReviewBritish journal of pharmacology2015

The effects of microRNA on the absorption, distribution, metabolism and excretion of drugs.

Y He, J R Chevillet, G Liu, T K Kim, K Wang

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Promises and challenges in pharmacoepigenetics.Cambridge prisms. Precision medicine · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Germline variants in cancer therapy.Cancer drug resistance (Alhambra, Calif.) · 2019
    Review
  11. Article
  12. Overview of microRNA Modulation in Analgesic Research.Current protocols in pharmacology · 2017
    Review
  13. The Promises of Quantitative Proteomics in Precision Medicine.Journal of pharmaceutical sciences · 2017
    Article
  14. MiRNAs and miRNA Polymorphisms Modify Drug Response.International journal of environmental research and public health · 2016
    Review
  15. Article
  16. Epigenetics and pharmacology.British journal of pharmacology · 2015
    Article
  17. Review
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

5 authors at 3 institutions in 2 countries.

Y HeInstitute of Medical Systems Biology, Guangdong Medical College, Dongguan, Guangdong, China.
J R ChevilletInstitute for Systems Biology, Seattle, WA, USA.
G LiuDepartment of Chemistry and Biochemistry, North Dakota State University, Fargo, ND, USA.
T K KimInstitute for Systems Biology, Seattle, WA, USA.
K WangInstitute for Systems Biology, Seattle, WA, USA.
Institute for Systems Biology · USGuangdong Medical College · CNNorth Dakota State University · US

Funding

Quantitative Systems BiologyP50GM076547 · NIGMS · INSTITUTE FOR SYSTEMS BIOLOGY · PI DUDLEY, AIMEE M · 2006 to 2016
$30.6M
NIGMS NIH HHS P50 GM076547NIGMS NIH HHS P50GM076547
6 · The paper itself

Abstract

The importance of genetic factors (e.g. sequence variation) in the absorption, distribution, metabolism, excretion (ADME) and overall efficacy of therapeutic agents is well established. Our ability to identify, interpret and utilize these factors is the subject of much clinical investigation and therapeutic development. However, drug ADME and efficacy are also heavily influenced by epigenetic factors such as DNA/histone methylation and non-coding RNAs [especially microRNAs (miRNAs)]. Results from studies using tools, such as in silico miRNA target prediction, in vitro functional assays, nucleic acid profiling/sequencing and high-throughput proteomics, are rapidly expanding our knowledge of these factors and their effects on drug metabolism. Although these studies reveal a complex regulation of drug ADME, an increased understanding of the molecular interplay between the genome, epigenome and transcriptome has the potential to provide practically useful strategies to facilitate drug development, optimize therapeutic efficacy, circumvent adverse effects, yield novel diagnostics and ultimately become an integral component of personalized medicine.

Indexed as

Absorption, PhysiologicalBiotransformationCytochrome P-450 Enzyme SystemDNA MethylationGene Expression RegulationHumansMembrane Transport ProteinsMicroRNAsPharmaceutical PreparationsReceptors, Cytoplasmic and NuclearTranscriptomeCytochrome P-450 Enzyme SystemMembrane Transport ProteinsMicroRNAsPharmaceutical PreparationsReceptors, Cytoplasmic and Nuclear

Identifiers

PMID25296724
PMCPMC4439871
OpenAlexW1603480357

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.