Evidence map›Paper›PMID 27684561›Full record

ArticlePloS one

Effect of Polyaryl Hydrocarbons on Cytotoxicity in Monocytic Cells: Potential Role of Cytochromes P450 and Oxidative Stress Pathways.

Sabina Ranjit, Narasimha M Midde, Namita Sinha, Benjamin J Patters, Mohammad A Rahman, Theodore J Cory, P S S Rao, Santosh Kumar

Open access · goldAbstract read
In one paragraph

Article in PloS one. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 2 institutions in 1 country.

Sabina RanjitDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.
Narasimha M MiddeDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.
Namita SinhaDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.
Benjamin J PattersDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.
Mohammad A RahmanDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.
Theodore J CoryDepartment of Clinical Pharmacy, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.
P S S RaoDepartment of Pharmaceutical Sciences, The University of Findley, 1000 N. Main Street, Findlay, OH, 45840, United States of America.
Santosh KumarDepartment of Pharmaceutical Sciences, University of Tennessee Health Science Center, Memphis, TN, 38163, United States of America.ORCID http://orcid.org/0000-0001-7846-5674
University of Tennessee Health Science Center · USUniversity of Findlay · US

Funding

Exosomes in tobacco-and HIV-mediated neurotoxcityR21DA042374 · NIDA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KUMAR, SANTOSH · 2016 to 2017
$431k
NIDA NIH HHS R21 DA042374
6 · The paper itself

Abstract

backgroundBenzo(a)pyrene (BaP), naphthalene (NPh), phenanthrene (Phe), benzo(a)antharacene (BeA), and benzo(b)fluoranthene (BeF) are known carcinogenic polyaryl hydrocarbons (PAHs) present in cigarette smoke. This study was designed to examine the relative effect of these constituents on the cytotoxicity of monocytic cells and the possible mechanism of PAH-mediated cytotoxicity.

methodsWe examined the acute (6-24 hours) and chronic (7 days) effects of these PAHs on the expression of cytochromes P450 (CYPs), oxidative stress, and cytotoxicity. The treated cells were examined for mRNA and protein levels of CYPs (1A1 and 3A4) and antioxidants enzymes (AOEs) superoxide dismutase-1 (SOD1) and catalase. Further, we assessed the levels of reactive oxygen species (ROS), caspase-3 cleavage activity, and cell viability. We performed these experiments in U937 and/or primary monocytic cells.

resultsOf the five PAHs tested, after chronic treatment only BaP (100 nM) showed a significant increase in the expression of CYP1A1, AOEs (SOD1 and catalase), ROS generation, caspase-3 cleavage activity, and cytotoxicity. However, acute treatment with BaP showed only an increase in the mRNA expression of CYP1A1.

conclusionsThese results suggest that of the five PAHs tested, BaP is the major contributor to the toxic effect of PAHs in monocytic cells, which is likely to occur through CYP and oxidative stress pathways.

Identifiers

PMID27684561
PMCPMC5042547
OpenAlexW2525750312

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.