Evidence map›Paper›PMID 19597468›Full record

ArticleOncogene2009

Beta4 integrin promotes osteosarcoma metastasis and interacts with ezrin.

X Wan, S Y Kim, L M Guenther, A Mendoza, J Briggs, C Yeung, D Currier, H Zhang, C Mackall, W-J Li and 4 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Osteosarcoma mechanobiology and therapeutic targets.British journal of pharmacology · 2022
    Review
  5. Review
  6. Osteosarcoma and Metastasis.Frontiers in oncology · 2021
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. MicroRNA-451 dictates the anoikis resistance of osteosarcoma by targeting Rab14.International journal of clinical and experimental pathology · 2017
    Article
  19. Review
  20. 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.

X WanCenter for Cancer Research, National Cancer Institute, Bethesda, MD 20892-1928, USA. xiaolinw@mail.nih.gov
S Y Kim
L M Guenther
A Mendoza
J Briggs
C Yeung
D Currier
H Zhang
C Mackall
W-J Li
R S Tuan
A T Deyrup
C Khanna
L Helman
National Cancer Institute · USCenter for Cancer Research · USEmory University · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USNational Institutes of Health · US

Funding

Molecular Biology of Pediatric TumorsZIASC006892 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI HELMAN, LEE J. · 2009 to 2017
$6.3M
Clinical Program in Pediatric SarcomasZIABC011074 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MACKALL, CRYSTAL · 2009 to 2012
$5.2M
Solid TumorsZIASC006891 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI HELMAN, LEE J. · 2009 to 2017
$5.0M
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
Solid Tumors30Z01SC006891 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI HELMAN, LEE J. · 1996 to 2008
$1.4M
SOLID TUMORSZ01SC006892 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI HELMAN, LEE J. · 1996 to 2008
$1.2M
Cell and Molecular Biology of Skeletal DevelopmentZIAAR041131 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI TUAN, ROCKY S · 2009 to 2009
$703k
Intramural NIH HHS Z01 SC006891Intramural NIH HHS Z01 SC006892Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

The development of pulmonary metastasis is the major cause of death in osteosarcoma, and its molecular basis is poorly understood. In this study, we show that beta4 integrin is highly expressed in human osteosarcoma cell lines and tumor samples. Furthermore, highly metastatic MNNG-HOS cells have increased levels of beta4 integrin. Suppression of beta4 integrin expression by shRNA and disruption of beta4 integrin function by transfection of dominant-negative beta4 integrin was sufficient to revert this highly metastatic phenotype in the MNNG-HOS model without significantly affecting primary tumor growth. These findings suggest a role for beta4 integrin expression in the metastatic phenotype in human osteosarcoma cells. In addition, we identified a previously uncharacterized interaction between beta4 integrin and ezrin, a membrane-cytoskeletal linker protein that is implicated in the metastatic behavior of osteosarcoma. The beta4 integrin-ezrin interaction appears to be critical for maintenance of beta4 integrin expression. These data begin to integrate ezrin and beta4 integrin expression into a model of action for the mechanism of osteosarcoma metastases.

Indexed as

Bone NeoplasmsCell Line, TumorCytoskeletal ProteinsEzrinHumansIntegrin beta4OsteosarcomaCytoskeletal ProteinsEzrinIntegrin beta4

Identifiers

PMID19597468
PMCPMC2753583
OpenAlexW2006260464

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.