Evidence map›Paper›PMID 35701181›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2022

Thomas J DiProspero, Lauren G Brown, Trevor D Fachko, Matthew R Lockett

Open access · bronzeAbstract read
In one paragraph

Article in Drug metabolism and disposition: the biological fate of chemicals, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

4 authors at 1 institution in 1 country.

Thomas J DiProsperoChemistry, University of North Carolina at Chapel Hill, United States.
Lauren G BrownChemistry, Univeristy of North Carolina at Chapel Hill, United States.
Trevor D FachkoChemistry, University of North Carolina at Chapel Hill, United States.
Matthew R LockettChemistry, University of North Carolina at Chapel Hill, United States mlockett@unc.edu.ORCID 0000-0003-4851-7757
University of North Carolina at Chapel Hill · US

Funding

UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel · 2001 to 2026
$36.3M
Paper-based cultures supporting tissue-like structures for biochemical studies of oxygen gradients and screening applicationsR35GM128697 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Matthew Ryen Lockett · 2018 to 2026
$3.1M
NIEHS NIH HHS P30 ES010126NIGMS NIH HHS R35 GM128697
6 · The paper itself

Abstract

The cellular microenvironment plays an important role in liver zonation, the spatial distribution of metabolic tasks amongst hepatocytes lining the sinusoid. Standard tissue culture practices provide an excess of oxygen and a lack of signaling molecules typically found in the liver. We hypothesized that incorporating physiologically relevant environments would promote post-differentiation patterning of hepatocytes and result in zonal-like characteristics. To test this hypothesis, we evaluated the transcriptional regulation and activity of drug-metabolizing enzymes in HepaRG cells exposed to three different oxygen tensions, in the presence or absence of Wnt/β-catenin signaling. The drug-metabolizing activity of cells exposed to representative periportal (11% O

Indexed as

cytochrome P450drug metabolismhepatocytesin vitro toxicity assays

Identifiers

PMID35701181
PMCPMC9341261
OpenAlexW4282928161

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.