Evidence map›Paper›PMID 25735774›Full record

ArticleCancer discovery2015

Intratumoral heterogeneity in a Trp53-null mouse model of human breast cancer.

Mei Zhang, Anna Tsimelzon, Chi-Hsuan Chang, Cheng Fan, Andrew Wolff, Charles M Perou, Susan G Hilsenbeck, Jeffrey M Rosen

Open access · greenAbstract read
In one paragraph

Article in Cancer discovery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.0field-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

49 citing papers in PubMed, 73 citations in OpenAlex.

  1. Trial
  2. Article
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  4. Article
  5. CXCR4Nature communications · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Epithelial Stem Cells: Making, Shaping and Breaking the Niche.Advances in experimental medicine and biology · 2022
    Article
  13. Article
  14. Review
  15. Heterogeneity within molecular subtypes of breast cancer.American journal of physiology. Cell physiology · 2021
    Review
  16. In Silico Logical Modelling to Uncover Cooperative Interactions in Cancer.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Mei ZhangDepartment of Developmental Biology, University of Pittsburgh, Pittsburgh, Pennsylvania. meizhang@pitt.edu jrosen@bcm.edu.
Anna TsimelzonLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, Texas.
Chi-Hsuan ChangDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas.
Cheng FanLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Andrew WolffDepartment of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA.
Charles M PerouLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina. Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina. Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Susan G HilsenbeckLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, Texas.
Jeffrey M RosenDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas. meizhang@pitt.edu jrosen@bcm.edu.
Baylor College of Medicine · USUniversity of North Carolina at Chapel Hill · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KATHERINE A. HOADLEY · 1992 to 2026
$59.3M
Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Geoffrey A Preidis · 2001 to 2026
$28.3M
Virology CoreP30AI036211 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI LEWIS, DOROTHY E. · 1994 to 2015
$21.7M
The Core of the Computational BiologyU54CA149196 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2010 to 2015
$10.6M
MALAT1 lncRNA as a Therapeutic Target in Triple Negative Breast CancerR01CA016303 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ROSEN, JEFFREY MARK · 1985 to 2022
$8.1M
HORMONAL REGULATION OF BREAST CANCERR37CA016303 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ROSEN, JEFFREY MARK · 1989 to 2011
$7.3M
Therapeutic Targeting of Breast Cancer Tumor Initiating CellsR01CA148761 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEROU, CHARLES M, ROSEN, JEFFREY MARK · 2010 to 2025
$6.5M
Defining the role of the tumor-initiating cell niche in breast cancerR00CA142898 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ZHANG, MEI · 2012 to 2014
$725k
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
Defining the role of the tumor-initiating cell niche in breast cancerK99CA142898 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, MEI · 2010 to 2011
$279k
NCI NIH HHS CA016303NCI NIH HHS CA125123NCI NIH HHS CA142898NCI NIH HHS CA148761NCI NIH HHS K99 CA142898NCI NIH HHS P30 CA047904NCI NIH HHS P30CA047904NCI NIH HHS P30 CA125123NCI NIH HHS P50 CA058223NCI NIH HHS P50-CA058223NCI NIH HHS R00 CA142898NCI NIH HHS R01 CA016303NCI NIH HHS R01 CA148761NCI NIH HHS R37 CA016303NCI NIH HHS U54 CA149196NCRR NIH HHS S10 RR024574NCRR NIH HHS S10RR024574NIAID NIH HHS P30 AI036211NIDDK NIH HHS DK56338NIDDK NIH HHS P30 DK056338
6 · The paper itself

Abstract

unlabelledIntratumoral heterogeneity correlates with clinical outcome and reflects the cellular complexity and dynamics within a tumor. Such heterogeneity is thought to contribute to radio- and chemoresistance because many treatments may target only certain tumor cell subpopulations. A better understanding of the functional interactions between various subpopulations of cells, therefore, may help in the development of effective cancer treatments. We identified a unique subpopulation of tumor cells expressing mesenchymal-like markers in a Trp53-null mouse model of basal-like breast cancer using fluorescence-activated cell sorting and microarray analysis. Both in vitro and in vivo experiments revealed the existence of cross-talk between these "mesenchymal-like" cells and tumor-initiating cells. Knockdown of genes encoding ligands upregulated in the mesenchymal cells and their corresponding receptors in the tumor-initiating cells resulted in reduced tumorigenicity and increased tumor latency. These studies illustrate the non-cell-autonomous properties and importance of cooperativity between tumor subpopulations. SIGNIFICANCE: Intratumoral heterogeneity has been considered one important factor in assessing a patient's initial response to treatment and selecting drug regimens to effectively increase tumor response rate. Elucidating the functional interactions between various subpopulations of tumor cells will help provide important new insights in understanding treatment response and tumor progression.

Indexed as

AnimalsAntigens, SurfaceBiomarkers, TumorBreast NeoplasmsCell CycleCell Self RenewalCell Transformation, NeoplasticCoculture TechniquesDisease Models, AnimalDown-RegulationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunophenotypingMiceAntigens, SurfaceBiomarkers, TumorTumor Suppressor Protein p53

Identifiers

PMID25735774
PMCPMC4420701
OpenAlexW2128527767

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.