Evidence map›Paper›PMID 28270621›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Integrin-β4 identifies cancer stem cell-enriched populations of partially mesenchymal carcinoma cells.

Brian Bierie, Sarah E Pierce, Cornelia Kroeger, Daniel G Stover, Diwakar R Pattabiraman, Prathapan Thiru, Joana Liu Donaher, Ferenc Reinhardt, Christine L Chaffer, Zuzana Keckesova and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 225 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
225citing papers in PubMed, 2 pooled it
14.7field-weighted citation impact, top 1% 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

225 citing papers in PubMed, 2 syntheses or guidelines pooled it, 363 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Review
  6. Targeting the Barriers Driving Immune Exclusion.Pharmaceuticals (Basel, Switzerland) · 2026
    Review
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  16. LMO2 Regulates Epithelial-Mesenchymal Plasticity of Mammary Epithelial Cells.Journal of mammary gland biology and neoplasia · 2026
    Article
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  18. Review
  19. Review
  20. Article

165 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

11 authors at 3 institutions in 1 country.

Brian BierieWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Sarah E PierceDepartment of Biology, Brown University, Providence, RI 02912.
Cornelia KroegerWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Daniel G StoverDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115.
Diwakar R PattabiramanWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Prathapan ThiruWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Joana Liu DonaherWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Ferenc ReinhardtWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Christine L ChafferWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Zuzana KeckesovaWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Robert A WeinbergWhitehead Institute for Biomedical Research, Cambridge, MA 02142; weinberg@wi.mit.edu.
Whitehead Institute for Biomedical Research · USBrown University · USDana-Farber Cancer Institute · US

Funding

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
Induced Differentiation to Deplete CSCs from Breast CancerR01CA078461 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI WEINBERG, ROBERT A · 1999 to 2017
$8.5M
Exploiting the epithelial-to-mesenchymal transition for the differentiation of cancer stem cellsK99CA201574 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI PATTABIRAMAN, DIWAKAR R · 2016 to 2017
$202k
NCI NIH HHS K99 CA201574NCI NIH HHS P01 CA080111NCI NIH HHS R01 CA078461
6 · The paper itself

Abstract

Neoplastic cells within individual carcinomas often exhibit considerable phenotypic heterogeneity in their epithelial versus mesenchymal-like cell states. Because carcinoma cells with mesenchymal features are often more resistant to therapy and may serve as a source of relapse, we sought to determine whether such cells could be further stratified into functionally distinct subtypes. Indeed, we find that a basal epithelial marker, integrin-β4 (ITGB4), can be used to enable stratification of mesenchymal-like triple-negative breast cancer (TNBC) cells that differ from one another in their relative tumorigenic abilities. Notably, we demonstrate that ITGB4

Indexed as

CarcinomaCell Line, TumorEpithelial-Mesenchymal TransitionFemaleHumansIntegrin beta4MesodermNeoplastic Stem CellsPrognosisTranscription FactorsTriple Negative Breast NeoplasmsTumor Suppressor ProteinsZinc Finger E-box-Binding Homeobox 1Integrin beta4ITGB4 protein, humanTP63 protein, humanTranscription FactorsTumor Suppressor ProteinsZinc Finger E-box-Binding Homeobox 1cancerEMTheterogeneityITGB4mesenchymal

Identifiers

PMID28270621
PMCPMC5373369
OpenAlexW2593940162

What OpenQuestion holds

Textmetadata
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.