Evidence map›Paper›PMID 30086285›Full record

ArticleBiochemical pharmacology2018

Quantitative characterization of UDP-glucuronosyltransferase 2B17 in human liver and intestine and its role in testosterone first-pass metabolism.

Haeyoung Zhang, Abdul Basit, Diana Busch, King Yabut, Deepak Kumar Bhatt, Marek Drozdzik, Marek Ostrowski, Albert Li, Carol Collins, Stefan Oswald and 1 more

Open access · greenAbstract read
In one paragraph

Article in Biochemical pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Curcumin enhances the oral bioavailability of testosterone by inhibiting its intestinal metabolism.Drug metabolism and disposition: the biological fate of chemicals · 2025
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Relevance of Human Aldoketoreductases and MicrobialDrug metabolism and disposition: the biological fate of chemicals · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. The Roles of Androgens in Humans: Biology, Metabolic Regulation and Health.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Quantitative Investigation of Irinotecan Metabolism, Transport, and Gut Microbiome Activation.Drug metabolism and disposition: the biological fate of chemicals · 2021
    Article
  17. Review
  18. Enzyme Kinetics of Uridine Diphosphate Glucuronosyltransferases (UGTs).Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  19. Review
  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

11 authors at 4 institutions in 3 countries.

Haeyoung ZhangDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Abdul BasitDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Diana BuschDepartment of Clinical Pharmacology, University of Greifswald, Greifswald, Germany.
King YabutDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Deepak Kumar BhattDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Marek DrozdzikDepartment of Experimental and Clinical Pharmacology, Pomeranian Medical University, Szczecin, Poland.
Marek OstrowskiDepartment of General and Transplantation Surgery, Pomeranian Medical University, Szczecin, Poland.
Albert LiIn Vitro ADMET Laboratories (IVAL), Columbia, MD, USA.
Carol CollinsDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Stefan OswaldDepartment of Clinical Pharmacology, University of Greifswald, Greifswald, Germany.
Bhagwat PrasadDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA. Electronic address: bhagwat@uw.edu.
University of Washington · USPomeranian Medical University · PLUniversität Greifswald · DEIn Vitro Admet Laboratories (United States) · US

Funding

Pharmacological Sciences SupplementT32GM007750 · NIGMS · UNIVERSITY OF WASHINGTON · PI ATKINS, WILLIAM M · 1985 to 2023
$12.6M
PBPK prediction of ontogeny mediated alteration in hepatic drug eliminationR01HD081299 · NICHD · WASHINGTON STATE UNIVERSITY · PI PRASAD, BHAGWAT · 2015 to 2025
$4.6M
NICHD NIH HHS R01 HD081299NIGMS NIH HHS T32 GM007750
6 · The paper itself

Abstract

Protein abundance and activity of UGT2B17, a highly variable drug- and androgen-metabolizing enzyme, were quantified in microsomes, S9 fractions, and primary cells isolated from human liver and intestine by validated LC-MS/MS methods. UGT2B17 protein abundance showed >160-fold variation (mean ± SD, 1.7 ± 2.7 pmol/mg microsomal protein) in adult human liver microsomes (n = 26) and significant correlation (r

Indexed as

EnterocytesEnzyme InhibitorsGene Expression Regulation, EnzymologicGlucuronosyltransferaseHepatocytesHumansImatinib MesylateMicrosomesMinor Histocompatibility AntigensTestosteroneEnzyme InhibitorsGlucuronosyltransferaseImatinib MesylateMinor Histocompatibility AntigensTestosteroneUGT2B17 protein, humanFirst-pass metabolismGlucuronidationInter-individual variabilityMetabolomicsTestosteroneUGT2B17

Identifiers

PMID30086285
PMCPMC6188809
OpenAlexW2887505080

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.