Evidence map›Paper›PMID 26246600›Full record

ArticleMolecular biology of the cell2015

Ezrin regulates focal adhesion and invadopodia dynamics by altering calpain activity to promote breast cancer cell invasion.

Victoria Hoskin, Alvin Szeto, Abdi Ghaffari, Peter A Greer, Graham P Côté, Bruce E Elliott

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 70 citations in OpenAlex.

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  15. Mechanosensitive channel Piezo1 is required for pulmonary artery smooth muscle cell proliferation.American journal of physiology. Lung cellular and molecular physiology · 2022
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  18. Osteosarcoma mechanobiology and therapeutic targets.British journal of pharmacology · 2022
    Review
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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

6 authors at 1 institution in 1 country.

Victoria HoskinDivision of Cancer Biology and Genetics, Cancer Research Institute, Queen's University, Kingston, ON K7L 3N6, Canada Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON K7L 3N6, Canada.
Alvin SzetoDivision of Cancer Biology and Genetics, Cancer Research Institute, Queen's University, Kingston, ON K7L 3N6, Canada Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON K7L 3N6, Canada.
Abdi GhaffariDivision of Cancer Biology and Genetics, Cancer Research Institute, Queen's University, Kingston, ON K7L 3N6, Canada Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON K7L 3N6, Canada.
Peter A GreerDivision of Cancer Biology and Genetics, Cancer Research Institute, Queen's University, Kingston, ON K7L 3N6, Canada Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON K7L 3N6, Canada.
Graham P CôtéDepartment of Biomedical and Molecular Sciences, Queen's University, Kingston, ON K7L 3N6, Canada.
Bruce E ElliottDivision of Cancer Biology and Genetics, Cancer Research Institute, Queen's University, Kingston, ON K7L 3N6, Canada Department of Pathology and Molecular Medicine, Queen's University, Kingston, ON K7L 3N6, Canada elliottb@queensu.ca.
Queen's University · CA

Funding

Canadian Institutes of Health Research MOP-102644
6 · The paper itself

Abstract

Up-regulation of the cytoskeleton linker protein ezrin frequently occurs in aggressive cancer types and is closely linked with metastatic progression. However, the underlying molecular mechanisms detailing how ezrin is involved in the invasive and metastatic phenotype remain unclear. Here we report a novel function of ezrin in regulating focal adhesion (FA) and invadopodia dynamics, two key processes required for efficient invasion to occur. We show that depletion of ezrin expression in invasive breast cancer cells impairs both FA and invadopodia turnover. We also demonstrate that ezrin-depleted cells display reduced calpain-mediated cleavage of the FA and invadopodia-associated proteins talin, focal adhesion kinase (FAK), and cortactin and reduced calpain-1-specific membrane localization, suggesting a requirement for ezrin in maintaining proper localization and activity of calpain-1. Furthermore, we show that ezrin is required for cell directionality, early lung seeding, and distant organ colonization but not primary tumor growth. Collectively our results unveil a novel mechanism by which ezrin regulates breast cancer cell invasion and metastasis.

Indexed as

AnimalsBreast NeoplasmsCalpainCell AdhesionCell Line, TumorCell MovementCytoskeletal ProteinsCytoskeletonExtracellular MatrixEzrinFemaleFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsHEK293 CellsHeterograftsHumansCalpainCytoskeletal ProteinsEzrinFocal Adhesion Protein-Tyrosine KinasesTalin

Identifiers

PMID26246600
PMCPMC4591691
OpenAlexW2194684539

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.