Evidence map›Paper›PMID 28552654›Full record

ArticleBiochemical pharmacology2017

MicroRNA hsa-miR-370-3p suppresses the expression and induction of CYP2D6 by facilitating mRNA degradation.

Linjuan Zeng, Yinting Chen, Yong Wang, Li-Rong Yu, Bridgett Knox, Jiwei Chen, Tieliu Shi, Si Chen, Zhen Ren, Lei Guo and 6 more

Open access · greenAbstract read
In one paragraph

Article in Biochemical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Novel Approaches to Characterize Individual Drug Metabolism and Advance Precision Medicine.Drug metabolism and disposition: the biological fate of chemicals · 2023
    Review
  4. Does ethnicity impact CYP2D6 genotype-phenotype relationships?Clinical and translational science · 2023
    Article
  5. Article
  6. Review
  7. Review
  8. Processing body (P-body) and its mediators in cancer.Molecular and cellular biochemistry · 2022
    Review
  9. Article
  10. miR-15a-3p Protects Against Isoniazid-Induced Liver InjuryFrontiers in molecular biosciences · 2021
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

16 authors at 6 institutions in 2 countries.

Linjuan ZengDepartment of Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai 519000, China; National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Yinting ChenNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA; Department of Gastroenterology, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou 510120, China; Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China.
Yong WangNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Li-Rong YuNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Bridgett KnoxNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Jiwei ChenSchool of Life Sciences, East China Normal University, Shanghai 200241, China.
Tieliu ShiSchool of Life Sciences, East China Normal University, Shanghai 200241, China.
Si ChenNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Zhen RenNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Lei GuoNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Yuanfeng WuNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
David LiuLongevity Center, CHI St. Vincent Hospital, Little Rock, AR 72205, USA.
Kaihong HuangDepartment of Gastroenterology, Sun Yat-sen Memorial Hospital of Sun Yat-sen University, Guangzhou 510120, China; Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China.
Weida TongNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA.
Dianke YuNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA; School of Public Health, Qingdao University, Qingdao 266071, China. Electronic address: dianke.yu@fda.hhs.gov.
Baitang NingNational Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, USA. Electronic address: baitang.ning@fda.hhs.gov.
United States Food and Drug Administration · USNational Center for Toxicological Research · USEast China Normal University · CNCHI St. Vincent · USFifth Affiliated Hospital of Sun Yat-sen University · CNSun Yat-sen University · CN

Funding

Intramural FDA HHS FD999999
6 · The paper itself

Abstract

Cytochrome P450 2D6 (CYP2D6) participates in the metabolism of approximately 20-25% of prescribed drugs. Genetic polymorphisms influence the expression and/or activity of CYP2D6, and inter-individual differences in drug activation and elimination caused by CYP2D6 genetic variants were reported. However, little is known about the potential modulation of CYP2D6 expression by microRNAs (miRNAs). In the current study, by using in silico prediction of the stabilities of miRNA/mRNA complexes, we screened 38 miRNA candidates that may interact with the transcript of CYP2D6. An inverse correlation between the expression of miRNA hsa-miR-370-3p and the expression of CYP2D6 was observed in human liver tissue samples. Electrophoretic mobility shift assays confirmed that hsa-miR-370-3p was able to directly bind to its cognate target within the coding region of the CYP2D6 transcript. The transfection of hsa-miR-370-3p mimics into the HepG2

Indexed as

Epigenesis, GeneticCell LineComputational BiologyCytochrome P-450 CYP2D6Cytochrome P-450 CYP2D6 InducersDatabases, ProteinDexamethasoneElectrophoretic Mobility Shift AssayEnzyme InductionEnzyme RepressionExpert SystemsGlucocorticoidsHepatocytesHumansHydrolysisMicroRNAsCytochrome P-450 CYP2D6Cytochrome P-450 CYP2D6 InducersDexamethasoneGlucocorticoidsMicroRNAsMIRN370 microRNA, humanRecombinant ProteinsRNA, MessengerCYP2D6Drug metabolizing enzymesEpigeneticshsa-miR-370-3pPharmacogenomics

Identifiers

PMID28552654
PMCPMC5687086
OpenAlexW2619099958

What OpenQuestion holds

Textmetadata
LicenceTDM
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.