Evidence map›Paper›PMID 23770079›Full record

ArticleCell stem cell2013

Molecular profiling of human mammary gland links breast cancer risk to a p27(+) cell population with progenitor characteristics.

Sibgat Choudhury, Vanessa Almendro, Vanessa F Merino, Zhenhua Wu, Reo Maruyama, Ying Su, Filipe C Martins, Mary Jo Fackler, Marina Bessarabova, Adam Kowalczyk and 35 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Epigenetic and Immune Mechanisms Linking Breastfeeding to Lower Breast Cancer Rates.Medical science monitor : international medical journal of experimental and clinical research · 2024
    Review
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  7. Article
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  14. Cell-type-specific epigenomic variations associated withNAR genomics and bioinformatics · 2022
    Article
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

45 authors at 12 institutions in 5 countries.

Sibgat ChoudhuryDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Vanessa Almendro
Vanessa F Merino
Zhenhua Wu
Reo Maruyama
Ying Su
Filipe C Martins
Mary Jo Fackler
Marina Bessarabova
Adam Kowalczyk
Thomas Conway
Bryan Beresford-Smith
Geoff Macintyre
Yu-Kang Cheng
Zoila Lopez-Bujanda
Antony Kaspi
Rong Hu
Judith Robens
Tatiana Nikolskaya
Vilde D Haakensen
Stuart J Schnitt
Pedram Argani
Gabrielle Ethington
Laura Panos
Michael Grant
Jason Clark
William Herlihy
S Joyce Lin
Grace Chew
Erik W Thompson
April Greene-Colozzi
Andrea L Richardson
Gedge D Rosson
Malcolm Pike
Judy E Garber
Yuri Nikolsky
Joanne L Blum
Alfred Au
E Shelley Hwang
Rulla M Tamimi
Franziska Michor
Izhak Haviv
X Shirley Liu
Saraswati Sukumar
Kornelia Polyak
Brigham and Women's Hospital · USThe University of Melbourne · AUJohns Hopkins University · USTexas Oncology · USHarvard University · USThomson Reuters (United States) · USBaker Heart and Diabetes Institute · AUBeth Israel Deaconess Medical Center · USDana-Farber Cancer Institute · USUniversity of Southern California · USOslo University Hospital · NOUniversity of California, San Francisco · US

Funding

Statistical MethodsP01CA087969 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI TWOROGER, SHELLEY S · 2000 to 2019
$77.8M
Use of Organotypic and Mammary Gland Models to Investigate the Outcomes of ClonalP01CA080111 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI DILLON, DEBORAH · 1999 to 2018
$36.0M
Variation in Receptor Tyrosine Kinases and Breast Cancer RiskP50CA089393 · NCI · DANA-FARBER CANCER INSTITUTE · PI HARRIS, LYNDSAY NORINE · 2000 to 2009
$28.8M
Epithelial-stromal cell interactions in breast cancerR01CA116235 · NCI · DANA-FARBER CANCER INST · PI POLYAK, KORNELIA · 2006 to 2010
$1.8M
NCI NIH HHS CA087969NCI NIH HHS CA116235-04S1NCI NIH HHS P01 CA080111NCI NIH HHS P01 CA087969NCI NIH HHS P50 CA089393NCI NIH HHS P50 CA89383NCI NIH HHS R01 CA116235
6 · The paper itself

Abstract

Early full-term pregnancy is one of the most effective natural protections against breast cancer. To investigate this effect, we have characterized the global gene expression and epigenetic profiles of multiple cell types from normal breast tissue of nulliparous and parous women and carriers of BRCA1 or BRCA2 mutations. We found significant differences in CD44(+) progenitor cells, where the levels of many stem cell-related genes and pathways, including the cell-cycle regulator p27, are lower in parous women without BRCA1/BRCA2 mutations. We also noted a significant reduction in the frequency of CD44(+)p27(+) cells in parous women and showed, using explant cultures, that parity-related signaling pathways play a role in regulating the number of p27(+) cells and their proliferation. Our results suggest that pathways controlling p27(+) mammary epithelial cells and the numbers of these cells relate to breast cancer risk and can be explored for cancer risk assessment and prevention.

Indexed as

Cell LineageGene Expression ProfilingBiomarkersBlotting, WesternBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCell DifferentiationCell ProliferationCells, CulturedCyclin-Dependent Kinase Inhibitor p27Epithelial CellsFemaleFibroblastsFlow CytometryFluorescent Antibody TechniqueBiomarkersBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanCDKN1B protein, humanCyclin-Dependent Kinase Inhibitor p27RNA, Messenger

Identifiers

PMID23770079
PMCPMC3703476
OpenAlexW2074581450

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.