Evidence map›Paper›PMID 22078097›Full record

ReviewBreast cancer research : BCR2011

Breast cancer epithelial-to-mesenchymal transition: examining the functional consequences of plasticity.

David J Drasin, Tyler P Robin, Heide L Ford

Open access · goldAbstract readReview
In one paragraph

Review in Breast cancer research : BCR, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 2% 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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 161 citations in OpenAlex.

  1. Pooled it
  2. Multi-omic Profiling of Recurrence Risk Across Breast Cancer Subtypes.medRxiv : the preprint server for health sciences · 2026
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  12. The TGFβ2-Snail1-miRNAClinical and translational medicine · 2024
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37 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

3 authors at 1 institution in 1 country.

David J DrasinDepartment of Obstetrics and Gynecology, University of Colorado Anschutz Medical Campus, 12700 E, 19th Ave, MS 8613, Aurora, CO 80045, USA.
Tyler P Robin
Heide L Ford
University of Colorado Anschutz Medical Campus · US

Funding

Medical Scientist Training ProgramT32GM008497 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI WILSON, CARA C. · 1993 to 2022
$15.2M
Role of Six1 in EMT and Tumor ProgressionR01CA095277 · NCI · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L. · 2002 to 2017
$4.3M
The Six1/Eya Transcriptional complex as a mediator of lymphangiogenesis and lymphR01CA157790 · NCI · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L. · 2011 to 2015
$1.8M
TRAIL Receptor Signaling in Human TumorsR01CA124545 · NCI · UNIVERSITY OF COLORADO DENVER · PI BEHBAKHT, KIAN, FORD, HEIDE L. · 2008 to 2011
$1.7M
NCI NIH HHS 1R01-CA124545-01NCI NIH HHS 1R01-CA157790NCI NIH HHS 2R01-CA095277NCI NIH HHS R01 CA095277NIGMS NIH HHS T32 GM008497
6 · The paper itself

Abstract

The epithelial-to-mesenchymal transition (EMT) is a critical developmental process that has recently come to the forefront of cancer biology. In breast carcinomas, acquisition of a mesenchymal-like phenotype that is reminiscent of an EMT, termed oncogenic EMT, is associated with pro-metastatic properties, including increased motility, invasion, anoikis resistance, immunosuppression and cancer stem cell characteristics. This oncogenic EMT is a consequence of cellular plasticity, which allows for interconversion between epithelial and mesenchymal-like states, and is thought to enable tumor cells not only to escape from the primary tumor, but also to colonize a secondary site. Indeed, the plasticity of cancer cells may explain the range of pro-metastatic traits conferred by oncogenic EMT, such as the recently described link between EMT and cancer stem cells and/or therapeutic resistance. Continued research into this relationship will be critical in developing drugs that block mechanisms of breast cancer progression, ultimately improving patient outcomes.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsBreast NeoplasmsFemaleHumansNeoplasm MetastasisNeoplastic Stem Cells

Identifiers

PMID22078097
PMCPMC3326549
OpenAlexW1977186103

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.