Evidence map›Paper›PMID 11259684›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2001

Role of the cytoplasmic tyrosines of beta 1A integrins in transformation by v-src.

T Sakai, R Jove, R Fässler, D F Mosher

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 81 citations in OpenAlex.

  1. α(M)β(2) integrin-mediated adhesion and motility of IL-5-stimulated eosinophils on periostin.American journal of respiratory cell and molecular biology · 2013
    Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Beta1 integrin cytoplasmic tyrosines promote skin tumorigenesis independent of their phosphorylation.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The final steps of integrin activation: the end game.Nature reviews. Molecular cell biology · 2010
    Review
  18. Article
  19. Src kinases as therapeutic targets for cancer.Nature reviews. Clinical oncology · 2009
    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

4 authors at 3 institutions in 2 countries.

T SakaiDepartment of Medicine and University of Wisconsin Comprehensive Cancer Center, University of Wisconsin, 1300 University Avenue, Madison, WI 53706, USA.
R Jove
R Fässler
D F Mosher
Moffitt Cancer Center · USLund University · SEMolecular Oncology (United States) · US

Funding

SCOR--CELLULAR AND MOLECULAR MECHANISMS OF ASTHMAP50HL056396 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MALTER, JAMES S · 1997 to 2006
$13.8M
STUDIES OF FIBRONECTIN AND RELATED GLYCOPROTEINSR01HL021644 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI MOSHER, DEANE FREMONT · 1985 to 2010
$3.2M
NHLBI NIH HHS HL21644NHLBI NIH HHS HL56396NHLBI NIH HHS P50 HL056396NHLBI NIH HHS R01 HL021644
6 · The paper itself

Abstract

GD25 cells lacking beta 1 integrins or expressing beta 1A with mutations of conserved cytoplasmic tyrosines (Y783, Y795) to phenylalanine have poor directed migration to platelet-derived growth factor or lysophosphatidic acid when compared with GD25 cells expressing wild-type beta 1A. We studied the effects of v-src on these cells. Transformation with v-src caused tyrosine and serine phosphorylation of wild-type beta1 A but not of Y783/795F doubly mutated beta 1A. v-src-transformed cells had rounded and/or fusiform morphology and poor assembly of fibronectin matrix. Adhesion to fibronectin or laminin and coupling of focal contacts to actin-containing cytoskeleton were preserved in transformed Y783/795F cells but lost on transformation when beta 1A was wild type. Transformed Y783/795F cells also retained ability, albeit limited, to migrate across filters, whereas transformed cells with wild-type beta 1A were unable to transverse filters. Studies of single tyrosine mutants showed that the more important tyrosine for retaining ability to adhere, assemble focal contacts, and migrate is Y783. These results suggest that overactive phosphorylation of cytoplasmic residues of beta 1A, particularly Y783, accounts in part for the phenotype of v-src-transformed cells.

Indexed as

ActinsAnimalsCell AdhesionCell MovementCells, CulturedCell Transformation, NeoplasticCytoplasmCytoskeletonFibronectinsFocal AdhesionsIntegrin beta1MiceOncogene Protein pp60(v-src)PhosphorylationTyrosineActinsFibronectinsIntegrin beta1Oncogene Protein pp60(v-src)Tyrosine

Identifiers

PMID11259684
PMCPMC31134
OpenAlexW1965871583

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.