Evidence map›Paper›PMID 31988452›Full record

ArticleOncogene2020

Cytokeratin 5 alters β-catenin dynamics in breast cancer cells.

Olivia McGinn, Ashley V Ward, Lynsey M Fettig, Duncan Riley, Joshua Ivie, Kiran V Paul, Peter Kabos, Jessica Finlay-Schultz, Carol A Sartorius

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Sialyl LewisCancers · 2023
    Article
  12. Review
  13. Essential role of aerobic glycolysis in epithelial-to-mesenchymal transition during carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  14. Article
  15. Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex.International journal of molecular sciences · 2021
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
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 at 1 institution in 1 country.

Olivia McGinnDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Ashley V WardDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Lynsey M FettigDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Duncan RileyDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Joshua IvieDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Kiran V PaulDivision of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Peter KabosDivision of Medical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Jessica Finlay-SchultzDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Carol A SartoriusDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA. Carol.Sartorius@cuanschutz.edu.
University of Colorado Anschutz Medical Campus · US

Funding

ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
Training Program in Cancer BiologyT32CA190216 · NCI · UNIVERSITY OF COLORADO DENVER · PI Craig T. Jordan · 2016 to 2026
$3.5M
Hormones and Tumor Initiating Cells in Human Breast CancersR01CA140985 · NCI · UNIVERSITY OF COLORADO DENVER · PI SARTORIUS, CAROL ANN · 2011 to 2020
$3.0M
Cancer-associated fibroblasts in estrogen receptor positive breast cancer.R01CA205044 · NCI · UNIVERSITY OF COLORADO DENVER · PI KABOS, PETER · 2016 to 2020
$1.8M
Neuronal Transdifferention in vivo: Mechanism and PotentialR01NS086839 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2014 to 2018
$1.7M
Cytokeratin 5/Beta-catenin interaction and crosstalk in hormone regulated breast cancer stem cellsF31CA232456 · NCI · UNIVERSITY OF COLORADO DENVER · PI MCGINN, OLIVIA F · 2019 to 2020
$70k
NCI NIH HHS F31 CA232456NCI NIH HHS R01 CA140985NCI NIH HHS R01 CA205044NCI NIH HHS T32 CA190216NINDS NIH HHS P30 NS048154NINDS NIH HHS R01 NS086839
6 · The paper itself

Abstract

Estrogen receptor (ER) positive breast cancers often contain subpopulations of cells that express the intermediate filament protein cytokeratin 5 (CK5). CK5+ cells are enriched in cancer stem cell (CSC) properties, can be induced by progestins, and predict poor prognosis in ER+ breast cancer. We established through CK5 knockout and overexpression in ER+ breast cancer cell lines that CK5 is important for tumorsphere formation, prompting us to speculate that CK5 has regulatory activity in CSCs. To interrogate CK5 interacting proteins that may be functionally cooperative, we performed immunoprecipitation-mass spectrometry for CK5 in ER+ breast cancer cells. Focusing on proteins with signaling activity, we identified β-catenin, a key transcription factor of the Wnt signaling pathway and cell adhesion molecule, as a CK5 interactor, which we confirmed by co-immunoprecipitation in several breast cancer models. We interrogated the dual functions of β-catenin in relation to CK5. Knockout or knockdown of CK5 ablated β-catenin transcriptional activity in response to progestins and Wnt stimuli. Conversely, CK5 induced by progestins or overexpression was sufficient to promote the loss of β-catenin at the cell membrane and total E-cadherin loss. A breast cancer patient-derived xenograft showed similar loss of membrane β-catenin and E-cadherin in CK5+ but not intratumoral CK5- cells and single-cell RNA sequencing found the top enriched pathways in the CK5+ cell cluster were cell junction remodeling and signaling. This report highlights that CK5 actively remodels cell morphology and that blockade of CK5-β-catenin interaction may reverse the detrimental properties of CK5+ breast cancer cells.

Indexed as

Adherens JunctionsAnimalsAntigens, CDbeta CateninBreast NeoplasmsCadherinsCarcinogenesisCell Line, TumorCell MembraneFemaleGene Knockout TechniquesHumansImmunoprecipitationKeratin-5Mass SpectrometryMiceAntigens, CDbeta CateninCadherinsCDH1 protein, humanKeratin-5KRT5 protein, humanProgestinsReceptors, Estrogen

Identifiers

PMID31988452
PMCPMC7085458
OpenAlexW3000785328

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.