Evidence map›Paper›PMID 23703818›Full record

ArticleHuman & experimental toxicology2014

Metabolism of the environmental toxicant benzo(a)pyrene by subcellular fractions of human ovary.

P V Rekhadevi, D L Diggs, A C Huderson, K L Harris, A E Archibong, A Ramesh

Open access · greenAbstract read
In one paragraph

Article in Human & experimental toxicology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-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

8 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Effects of Benzo[a]pyrene on Human Sperm Functions: An In Vitro Study.International journal of molecular sciences · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. In Vitro Co-Exposure to CeONanomaterials (Basel, Switzerland) · 2021
    Article
  7. Review
  8. 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

6 authors at 2 institutions in 1 country.

P V Rekhadevi1Department of Biochemistry and Cancer Biology, Meharry Medical College, Nashville, TN, USA.
D L Diggs
A C Huderson
K L Harris
A E Archibong
A Ramesh
Meharry Medical College · USEnvironmental Protection Agency · US

Funding

VITAMIN D DEFICIENCY AND INCREASED RISK OF UTERINE FIBROIDS IN AFRICAN AMERICANSG12RR003032 · NCRR · MEHARRY MEDICAL COLLEGE · PI HOLT, ROBERT G · 1985 to 2011
$27.4M
Translational Pathology CoreU54CA163069 · NCI · MEHARRY MEDICAL COLLEGE · PI BALLARD, BILLY RAY · 2011 to 2025
$18.8M
Mechanisms for Benzo(a)pyrene-Induced Colon Cancer Exacerbation by Dietary FatR01CA142845 · NCI · MEHARRY MEDICAL COLLEGE · PI RAMESH, ARAMANDLA · 2010 to 2013
$1.2M
Chemoprevention of colon cancer via neonatal imprintingR03CA130112 · NCI · MEHARRY MEDICAL COLLEGE · PI RAMESH, ARAMANDLA · 2007 to 2008
$147k
NCI NIH HHS 1R03CA130112-01NCI NIH HHS 5R01CA142845-04NCI NIH HHS R01 CA142845NCI NIH HHS R03 CA130112NCI NIH HHS U54 CA163069NCRR NIH HHS G12 RR003032NCRR NIH HHS G12 RR03032
6 · The paper itself

Abstract

Knowledge of the ability of the female reproductive system to metabolize environmental chemicals is critical not only from the standpoint of toxicity but also from infertility risk assessment. Benzo(a)pyrene (BaP) is a toxicant that is released into the environment from automobile exhausts, cigarette smoke, burning of refuse, industrial emissions, and hazardous waste sites. In exposed animals, BaP becomes activated to reactive metabolites that interfere with target organ function and as a consequence cause toxicity. Studies on animal models conducted in our laboratories and those of others have shown that BaP possess endocrine disrupting properties. Thus, this chemical has the potential to cause infertility and cancers in the female genital tract. An understanding of BaP metabolism in the female reproductive system will be of importance in the diagnosis and management of female fertility as well as cancers in the reproductive tissues. Therefore, the objective of our study was to examine the metabolism of BaP by human ovarian subcellular fractions. Human ovary samples (eight individuals) were obtained from postoperative tissue removed from subjects with uterine tumors. Subcellular fractions (nuclear, cytosolic, mitochondrial, and microsomal) were prepared by differential centrifugation. BaP (1 μM and 3 μM) was individually incubated with individual subcellular fractions for 15 min and the products were analyzed by high-performance liquid chromatography. Among the different fractions tested, microsomal BaP metabolism was higher than the rest of the fractions. The BaP metabolites identified were as follows: BaP-9,10-diol, BaP-4,5-diol, BaP-7,8-diol, 9(OH) BaP, 3(OH) BaP, BaP-1,6-dione, BaP-3,6-dione, and BaP-6,12-dione. Of interest was the presence of DNA-reactive metabolites such as BaP-3,6-dione, BaP-6,12-dione, and BaP 7,8-diol, which have been implicated in the causation of infertility and cancer. Our results indicate that women who are exposed to BaP via cigarette smoke, occupational settings, and diet are more likely at a larger risk of this toxicant-induced infertility and cancer than others.

Indexed as

Benzo(a)pyreneEnvironmental PollutantsFemaleHumansOvarySubcellular FractionsBenzo(a)pyreneEnvironmental PollutantsBenzo(a)pyreneinfertilitymetabolismovarysubcellular fractions

Identifiers

PMID23703818
PMCPMC4062653
OpenAlexW2070066938

What OpenQuestion holds

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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.