Evidence map›Paper›PMID 22859400›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2012

Age-associated gene expression in normal breast tissue mirrors qualitative age-at-incidence patterns for breast cancer.

Jason R Pirone, Monica D'Arcy, Delisha A Stewart, William C Hines, Melissa Johnson, Michael N Gould, Paul Yaswen, D Joseph Jerry, Sallie Smith Schneider, Melissa A Troester

Abstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. The DNA damage repair landscape in Black women with breast cancer.Therapeutic advances in medical oncology · 2022
    Article
  6. Article
  7. Article
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  11. Article
  12. Article
  13. Article
  14. Integrative analysis of pathway deregulation in obesity.NPJ systems biology and applications · 2017
    Article
  15. Article
  16. Cell Fate Decisions During Breast Cancer Development.Journal of developmental biology · 2016
    Article
  17. Article
  18. Article
  19. Article
  20. Tumor intrinsic subtype is reflected in cancer-adjacent tissue.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2015
    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

10 authors.

Jason R PironeLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Monica D'Arcy
Delisha A Stewart
William C Hines
Melissa Johnson
Michael N Gould
Paul Yaswen
D Joseph Jerry
Sallie Smith Schneider
Melissa A Troester

Funding

Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KATHERINE A. HOADLEY · 1992 to 2026
$59.3M
UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A. Troester · 2001 to 2026
$36.3M
Conserved Biology of Tumor and Microenvironment in Breast Cancer ProgressionR01CA138255 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEROU, CHARLES M, TROESTER, MELISSA A. · 2008 to 2012
$2.4M
Pregnancy, Obesogenic Environments, and Basal-like Breast CancerU01ES019472 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TROESTER, MELISSA A. · 2010 to 2014
$2.3M
Genetics of Breast Cancer Risk at Windows of ExposureU01ES019466 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI GOULD, MICHAEL N · 2010 to 2014
$2.2M
Breast Cancer GWAS: Function and Environmental InteractionsR01ES017400 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI GOULD, MICHAEL N, NEWTON, MICHAEL A · 2009 to 2013
$2.1M
P53-dependent responses to toxicants in parous and nulliparous breastR01ES015739 · NIEHS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI JERRY, D. JOSEPH · 2007 to 2010
$1.5M
NCI NIH HHS P50 CA058223NCI NIH HHS P50CA058223NCI NIH HHS R01 CA138255NCI NIH HHS R01-CA138255NIEHS NIH HHS P30 ES010126NIEHS NIH HHS R01 ES015739NIEHS NIH HHS R01 ES017400NIEHS NIH HHS R01-ES017400NIEHS NIH HHS U01 ES019466NIEHS NIH HHS U01-ES019466NIEHS NIH HHS U01 ES019472NIEHS NIH HHS U01-ES019472NIEHS NIH HHS U01-ES019548
6 · The paper itself

Abstract

backgroundAge is the strongest breast cancer risk factor, with overall breast cancer risk increasing steadily beginning at approximately 30 years of age. However, while breast cancer risk is lower among younger women, young women's breast cancer may be more aggressive. Although, several genomic and epidemiologic studies have shown higher prevalence of aggressive, estrogen-receptor negative breast cancer in younger women, the age-related gene expression that predisposes to these tumors is poorly understood. Characterizing age-related patterns of gene expression in normal breast tissues may provide insights on etiology of distinct breast cancer subtypes that arise from these tissues.

methodsTo identify age-related changes in normal breast tissue, 96 tissue specimens from patients with reduction mammoplasty, ages 14 to 70 years, were assayed by gene expression microarray.

resultsSignificant associations between gene expression levels and age were identified for 802 probes (481 increased, 321 decreased with increasing age). Enriched functions included "aging of cells," "shape change," and "chemotaxis," and enriched pathways included Wnt/beta-catenin signaling, Ephrin receptor signaling, and JAK/Stat signaling. Applying the age-associated genes to publicly available tumor datasets, the age-associated pathways defined two groups of tumors with distinct survival.

conclusionThe hazard rates of young-like tumors mirrored that of high-grade tumors in the Surveillance, Epidemiology, and End Results Program, providing a biologic link between normal aging and age-related tumor aggressiveness. IMPACT: These data show that studies of normal tissue gene expression can yield important insights about the pathways and biologic pressures that are relevant during tumor etiology and progression.

Indexed as

Gene Expression Regulation, NeoplasticAdolescentAdultAgedAge FactorsAgingBreastBreast NeoplasmsFemaleGene ExpressionHumansIncidenceMammaplastyMiddle AgedSignal Transduction

Identifiers

PMID22859400
PMCPMC3684707

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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.