Evidence map›Paper›PMID 22109888›Full record

ArticleEndocrinology2012

Neonatal exposure to estradiol/bisphenol A alters promoter methylation and expression of Nsbp1 and Hpcal1 genes and transcriptional programs of Dnmt3a/b and Mbd2/4 in the rat prostate gland throughout life.

Wan-yee Tang, Lisa M Morey, Yuk Yin Cheung, Lynn Birch, Gail S Prins, Shuk-mei Ho

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

81 citing papers in PubMed, 161 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. HPCAL1 is a novel driver of autophagy-dependent ferroptosis.Journal of Zhejiang University. Science. B · 2023
    Article
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  12. Review
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  16. Review
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21 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Wan-yee TangDepartment of Environmental Health, College of Medicine, University of Cincinnati, Cincinnati, Ohio 45267, USA.
Lisa M Morey
Yuk Yin Cheung
Lynn Birch
Gail S Prins
Shuk-mei Ho
University of Illinois Chicago · USCenter for Environmental Health · USUniversity of Cincinnati Medical Center · US

Funding

REPRODUCTIVE AND DEVELOPMENTAL TOXICOLOGY RESEARCHP30ES006096 · NIEHS · UNIVERSITY OF CINCINNATI · PI PINNEY, SUSAN MENGEL · 1992 to 2022
$35.4M
Training Program in Cancer TherapeuticsT32CA117846 · NCI · UNIVERSITY OF CINCINNATI · PI PRICE, CAROLYN M, TAKIAR, VINITA · 2006 to 2022
$6.5M
Epigenetic Basis for Prostate Carcinogenesis following Early Estrogenic ExposuresR01ES015584 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HO, SHUK-MEI, PRINS, GAIL S · 2008 to 2012
$3.1M
Development Estrogenization of the Rat Prostate GlandR01DK040890 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PRINS, GAIL S · 1996 to 2010
$2.9M
Susceptible Window of High Fat Diet/Bisphenol A Programming of Breast Cancer RiskU01ES019480 · NIEHS · UNIVERSITY OF CINCINNATI · PI HO, SHUK-MEI · 2010 to 2014
$2.2M
Developmental Reprogramming of Prostate Carcinogenesis by BPARC2ES018789 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HO, SHUK-MEI, MANCINI, MICHAEL A. · 2009 to 2010
$1.9M
Developmental Exposure to Low-dose Bisphenol A and Human Prostate Cancer SusceptiRC2ES018758 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI HO, SHUK-MEI, PRINS, GAIL S · 2009 to 2010
$1.9M
Hormone-induced inflammation and prostate cancerR01CA112532 · NCI · UNIVERSITY OF CINCINNATI · PI HO, SHUK-MEI · 2006 to 2009
$1.1M
Chronic exposure to Biphenol A and uterine cancer risk markersU01ES020988 · NIEHS · UNIVERSITY OF CINCINNATI · PI HO, SHUK-MEI · 2011 to 2014
$796k
Estrogens/Xenoestrogens and Epigenetic Regulation of Gene ExpressionR00ES016817 · NIEHS · JOHNS HOPKINS UNIVERSITY · PI TANG, WAN-YEE · 2010 to 2012
$747k
Estrogens/Xenoestrogens and Epigenetic Regulation of Gene ExpressionK99ES016817 · NIEHS · UNIVERSITY OF CINCINNATI · PI TANG, WAN-YEE · 2008 to 2009
$180k
Dietary Intervention for Bisphenol A-induced Susceptibility to Prostate NeoplasiaR03CA136023 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PRINS, GAIL S · 2008 to 2009
$157k
BLRD VA I01 BX000675NCI NIH HHS CA112532NCI NIH HHS CA136023NCI NIH HHS R01 CA112532NCI NIH HHS R03 CA136023NCI NIH HHS T32 CA117846NIDDK NIH HHS DK40890NIDDK NIH HHS R01 DK040890NIEHS NIH HHS ES006096NIEHS NIH HHS ES015584NIEHS NIH HHS ES016817NIEHS NIH HHS ES018758NIEHS NIH HHS ES018789NIEHS NIH HHS ES019480NIEHS NIH HHS ES020988NIEHS NIH HHS K99 ES016817NIEHS NIH HHS P30 ES006096NIEHS NIH HHS R00 ES016817NIEHS NIH HHS R01 ES015584NIEHS NIH HHS RC2 ES018758NIEHS NIH HHS RC2 ES018789NIEHS NIH HHS U01 ES019480NIEHS NIH HHS U01 ES020988
6 · The paper itself

Abstract

Evidence supporting an early origin of prostate cancer is growing. We demonstrated previously that brief exposure of neonatal rats to estradiol or bisphenol A elevated their risk of developing precancerous lesions in the prostate upon androgen-supported treatment with estradiol as adults. Epigenetic reprogramming may be a mechanism underlying this inductive event in early life, because we observed overexpression of phosphodiesterase 4D variant 4 (Pde4d4) through induction of hypomethylation of its promoter. This epigenetic mark was invisible in early life (postnatal d 10), becoming apparent only after sexual maturation. Here, we asked whether other estrogen-reprogrammable epigenetic marks have similar or different patterns in gene methylation changes throughout life. We found that hypomethylation of the promoter of nucleosome binding protein-1 (Nsbp1), unlike Pde4d4, is an early and permanent epigenetic mark of neonatal exposure to estradiol/bisphenol A that persists throughout life, unaffected by events during adulthood. In contrast, hippocalcin-like 1 (Hpcal1) is a highly plastic epigenetic mark whose hypermethylation depends on both type of early-life exposure and adult-life events. Four of the eight genes involved in DNA methylation/demethylation showed early and persistent overexpression that was not a function of DNA methylation at their promoters, including genes encoding de novo DNA methyltransferases (Dnmt3a/b) and methyl-CpG binding domain proteins (Mbd2/4) that have demethylating activities. Their lifelong aberrant expression implicates them in early-life reprogramming and prostate carcinogenesis during adulthood. We speculate that the distinctly different fate of early-life epigenetic marks during adulthood reflects the complex nature of lifelong editing of early-life epigenetic reprogramming.

Indexed as

AnimalsAnimals, NewbornAzacitidineBase SequenceBenzhydryl CompoundsBisphenol A CompoundsCalcium-Binding ProteinsDecitabineDNA-Binding ProteinsDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3ADNA Methyltransferase 3BDNA PrimersEstradiolGene ExpressionAzacitidineBenzhydryl Compoundsbisphenol ABisphenol A CompoundsCalcium-Binding ProteinsDecitabineDNA-Binding ProteinsDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDNA PrimersEstradiolHMGN ProteinsHpcal1 protein, ratMBD2 proteinNerve Tissue ProteinsPhenolsRNA, Small Interfering

Identifiers

PMID22109888
PMCPMC3249669
OpenAlexW2070584219

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.