Evidence map›Paper›PMID 22577345›Full record

ArticleNeoplasia (New York, N.Y.)2012

The ezrin metastatic phenotype is associated with the initiation of protein translation.

Joseph W Briggs, Ling Ren, Rachel Nguyen, Kristi Chakrabarti, Jessica Cassavaugh, Said Rahim, Gulay Bulut, Ming Zhou, Timothy D Veenstra, Qingrong Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Detecting the location and significance of Ezrin protein expression in hepatocellular carcinoma.International journal of clinical and experimental pathology · 2018
    Article
  6. Article
  7. Overexpression of ezrin and galectin-3 as predictors of poor prognosis of cervical cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2017
    Article
  8. mTOR Inhibition Mitigates Enhanced mRNA Translation Associated with the Metastatic Phenotype of Osteosarcoma Cells In Vivo.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    Article
  9. The clinical significance of changes in ezrin expression in osteosarcoma of children and young adults.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  10. Ezrin Inhibition Up-regulates Stress Response Gene Expression.The Journal of biological chemistry · 2016
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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

14 authors at 5 institutions in 1 country.

Joseph W BriggsTumor and Metastasis Biology Section, Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
Ling Ren
Rachel Nguyen
Kristi Chakrabarti
Jessica Cassavaugh
Said Rahim
Gulay Bulut
Ming Zhou
Timothy D Veenstra
Qingrong Chen
Jun S Wei
Javed Khan
Aykut Uren
Chand Khanna
Center for Cancer Research · USNational Cancer Institute · USGeorgetown University Medical Center · USGeorgetown University · USScience Applications International Corporation (United States) · US

Funding

BIOINFORMATICS: SYSTEMS BIOLOGY OF PEDIATRIC CANCERSZIABC011002 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KHAN, JAVED · 2009 to 2025
$9.3M
Tumor and Metastasis BiologyZIABC010566 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HELMAN, LEE J. · 2009 to 2017
$4.6M
Tumor and Metastasis TherapyZIABC011024 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KHANNA, CHAND · 2009 to 2013
$3.2M
6 · The paper itself

Abstract

We previously associated the cytoskeleton linker protein, Ezrin, with the metastatic phenotype of pediatric sarcomas, including osteosarcoma and rhabdomyosarcoma. These studies have suggested that Ezrin contributes to the survival of cancer cells after their arrival at secondary metastatic locations. To better understand this role in metastasis, we undertook two noncandidate analyses of Ezrin function including a microarray subtraction of high-and low-Ezrin-expressing cells and a proteomic approach to identify proteins that bound the N-terminus of Ezrin in tumor lysates. Functional analyses of these data led to a novel and unifying hypothesis that Ezrin contributes to the efficiency of metastasis through regulation of protein translation. In support of this hypothesis, we found Ezrin to be part of the ribonucleoprotein complex to facilitate the expression of complex messenger RNA in cells and to bind with poly A binding protein 1 (PABP1; PABPC1). The relevance of these findings was supported by our identification of Ezrin and components of the translational machinery in pseudopodia of highly metastatic cells during the process of cell invasion. Finally, two small molecule inhibitors recently shown to inhibit the Ezrin metastatic phenotype disrupted the Ezrin/PABP1 association. Taken together, these results provide a novel mechanistic basis by which Ezrin may contribute to metastasis.

Indexed as

Neoplasm InvasivenessBlotting, WesternCell LineCell Line, TumorCytoskeletal ProteinsEnzyme-Linked Immunosorbent AssayEzrinHumansImmunoprecipitationOligonucleotide Array Sequence AnalysisPhenotypeProtein BiosynthesisRNA, Small InterferingTandem Mass SpectrometryTransfectionCytoskeletal ProteinsEzrinRNA, Small Interfering

Identifiers

PMID22577345
PMCPMC3349256
OpenAlexW1839204217

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.