Evidence map›Paper›PMID 23999928›Full record

ReviewThe Prostate2013

Epigenetic susceptibility factors for prostate cancer with aging.

N A Damaschke, B Yang, S Bhusari, J P Svaren, D F Jarrard

Open access · greenAbstract readReview
In one paragraph

Review in The Prostate, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. RASSF1A and its epigenetic dysregulation in genitourinary cancer: a current update.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
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  18. Article
  19. Role of lncRNAs in aging and age-related diseases.Aging medicine (Milton (N.S.W)) · 2018
    Review
  20. 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

5 authors at 2 institutions in 1 country.

N A DamaschkeDepartment of Urology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
B Yang
S Bhusari
J P Svaren
D F Jarrard
University of Wisconsin–Madison · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

MODULATION OF IGF-II IMPRINTING IN THE AGING PROSTATER01CA097131 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI JARRARD, DAVID F. · 2002 to 2013
$2.5M
NCI NIH HHS R01 CA097131
6 · The paper itself

Abstract

backgroundIncreasing age is a significant risk factor for prostate cancer. The prostate is exposed to environmental and endogenous stress that may underlie this remarkable incidence. DNA methylation, genomic imprinting, and histone modifications are examples of epigenetic factors known to undergo change in the aging and cancerous prostate. In this review we examine the data linking epigenetic alterations in the prostate with aging to cancer development.

methodsAn online search of current and past peer reviewed literature on epigenetic changes with cancer and aging was performed. Relevant articles were analyzed.

resultsEpigenetic changes are responsible for modifying expression of oncogenes and tumor suppressors. Several of these changes may represent a field defect that predisposes to cancer development. Focal hypermethylation occurs at CpG islands in the promoters of certain genes including GSTP1, RARβ2, and RASSF1A with both age and cancer, while global hypomethylation is seen in prostate cancer and known to occur in the colon and other organs. A loss of genomic imprinting is responsible for biallelic expression of the well-known Insulin-like Growth Factor 2 (IGF2) gene. Loss of imprinting (LOI) at IGF2 has been documented in cancer and is also known to occur in benign aging prostate tissue marking the presence of cancer. Histone modifications have the ability to dictate chromatin structure and direct gene expression.

conclusionsEpigenetic changes with aging represent molecular mechanisms to explain the increased susceptibly of the prostate to develop cancer in older men. These changes may provide an opportunity for diagnostic and chemopreventive strategies given the epigenome can be modified.

Indexed as

AgingCpG IslandsDNA MethylationEpigenesis, GeneticGenetic Predisposition to DiseaseGenomic ImprintingHistonesHumansInsulin-Like Growth Factor IIMaleProstatic NeoplasmsRisk FactorsHistonesIGF2 protein, humanInsulin-Like Growth Factor IIagingepigeneticsimprintingmethylationprostate cancer

Identifiers

PMID23999928
PMCPMC4237278
OpenAlexW1537175468

What OpenQuestion holds

Textmetadata
LicenceTDM
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.