Evidence map›Paper›PMID 35752443›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2022

High-Throughput Production of Diverse Xenobiotic Metabolites with Cytochrome P450-Transduced Huh7 Hepatoma Cell Lines.

Choon-Myung Lee, Ken H Liu, Grant Singer, Gary W Miller, Shuzhao Li, Dean P Jones, Edward T Morgan

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 1 institution in 1 country.

Choon-Myung LeeDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.).
Ken H LiuDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.).
Grant SingerDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.).
Gary W MillerDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.).
Shuzhao LiDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.).
Dean P JonesDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.) etmorga@emory.edu dpjones@emory.edu.
Edward T MorganDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, Georgia (C.-m.L., G.S., E.T.M.); Clinical Biomarkers Laboratory, Department of Medicine, Emory University, Atlanta, Georgia (K.H.L., D.P.J.); Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, New York (G.W.M.); and The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut (S.L.) etmorga@emory.edu dpjones@emory.edu.ORCID 0000-0003-4273-2261
Emory University · US

Funding

Pilot Project ProgramP30ES019776 · NIEHS · EMORY UNIVERSITY · PI William Michael Caudle · 2013 to 2026
$22.6M
U2C Experimental CoreU2CES030163 · NIEHS · EMORY UNIVERSITY · PI JONES, DEAN PAUL, LI, SHUZHAO · 2018 to 2021
$3.6M
NIEHS NIH HHS P30 ES019776NIEHS NIH HHS U2C ES030163
6 · The paper itself

Abstract

Precision medicine and exposomics require methods to assess xenobiotic metabolism in human metabolomic analyses, including the identification of known and undocumented drug and chemical exposures as well as their metabolites. Recent work demonstrated the use of high-throughput generation of xenobiotic metabolites with human liver S-9 fractions for their detection in human plasma and urine. Here, we tested whether a panel of lentivirally transduced human hepatoma cell lines (Huh7) that express individual cytochrome P450 (P450) enzymes could be used to generate P450-specific metabolites in a high-throughput manner, while simultaneously identifying the enzymes responsible. Cell-line activities were verified using P450-specific probe substrates. To increase analytical throughput, we used a pooling strategy where 36 chemicals were grouped into 12 unique mixtures, each mixture containing 6 randomly selected compounds, and each compound being present in two separate mixtures. Each mixture was incubated with 8 different P450 cell lines for 0 and 2 hours and extracts were analyzed using liquid chromatography-high-resolution mass spectrometry. Cell lines selectively metabolized test substrates, e.g., pazopanib, bupropion, and

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsBupropionCell LineCytochrome P-450 Enzyme SystemHumansXenobioticsBupropionCytochrome P-450 Enzyme SystemXenobiotics

Identifiers

PMID35752443
PMCPMC9450959
OpenAlexW4283585864

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.