Evidence map›Paper›PMID 29968906›Full record

ReviewJournal of cellular physiology2018

Epithelial-to-mesenchymal transition and cancer stem cells contribute to breast cancer heterogeneity.

Deli Hong, Andrew J Fritz, Sayyed K Zaidi, Andre J van Wijnen, Jeffrey A Nickerson, Anthony N Imbalzano, Jane B Lian, Janet L Stein, Gary S Stein

Abstract readReview
In one paragraph

Review in Journal of cellular physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
–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

70 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

10 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

9 authors.

Deli HongDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Andrew J FritzDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.
Sayyed K ZaidiDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0001-6664-5168
Andre J van WijnenDepartments of Orthopedic Surgery and Biochemistry & Molecular Biology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-4458-0946
Jeffrey A NickersonDepartment of Pediatrics, UMass Medical School, Worcester, Massachusetts.
Anthony N ImbalzanoGraduate Program in Cell Biology and Department of Biochemistry and Molecular Pharmacology, UMass Medical School, Worcester, Massachusetts.
Jane B LianDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0001-8683-9138
Janet L SteinDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0002-2474-6822
Gary S SteinDepartment of Biochemistry and University of Vermont Cancer Center, University of Vermont, Burlington, Vermont.ORCID 0000-0001-8762-5422

Funding

Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI CLIFFORD JAMES ROSEN · 2017 to 2026
$51.6M
SUBNUCLEAR TARGETING OF TRANSCRIPTION FACTORSP01CA082834 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI STEIN, GARY S. · 2001 to 2015
$18.4M
Supplement to AWD32581 - Fritz fellowship F32CA220935F32CA220935 · NCI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI FRITZ, ANDREW J · 2018 to 2021
$216k
NCI NIH HHS F32 CA220935NCI NIH HHS P01 CA082834NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

Breast cancer is the most common cancer in women, and accounts for ~30% of new cancer cases and 15% of cancer-related deaths. Tumor relapse and metastasis are primary factors contributing to breast cancer-related deaths. Therefore, the challenge for breast cancer treatment is to sustain remission. A driving force behind tumor relapse is breast cancer heterogeneity (both intertumor, between different patients, and intratumor, within the same tumor). Understanding breast cancer heterogeneity is necessary to develop preventive interventions and targeted therapies. A recently emerging concept is that intratumor heterogeneity is driven by cancer stem cells (CSCs) that are capable of giving rise to a multitude of different cells within a tumor. Studies have highlighted linkage of CSC formation with epithelial-to-mesenchymal transition (EMT). In this review, we summarize the current understanding of breast cancer heterogeneity, links between EMT and CSCs, regulation of EMT by Runx transcription factors, and potential therapeutic strategies targeting these processes.

Indexed as

Breast NeoplasmsCarcinogenesisCore Binding Factor alpha SubunitsEpithelial-Mesenchymal TransitionFemaleGenetic HeterogeneityHumansNeoplastic Stem CellsCore Binding Factor alpha Subunitsbreast cancercancer stem cell (CSC)epithelial-to-mesenchymal transition (EMT)tumor heterogeneity

Identifiers

PMID29968906
PMCPMC6185773

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.