Evidence map›Paper›PMID 17544257›Full record

ArticleCellular signalling2007

Multiple proteins mediate IQGAP1-stimulated cell migration.

Jennifer M Mataraza, Zhigang Li, Ha-Won Jeong, Matthew D Brown, David B Sacks

Open access · greenAbstract read
In one paragraph

Article in Cellular signalling, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Calreticulin inhibits inflammation-induced osteoclastogenesis and bone resorption.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. IQGAP1: a regulator of intracellular spacetime relativity.Journal of immunology (Baltimore, Md. : 1950) · 2012
    Review
  12. Article
  13. Anchored protein kinase A recruitment of active Rac GTPase.The Journal of biological chemistry · 2011
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

5 authors at 2 institutions in 1 country.

Jennifer M MatarazaDepartment of Pathology, Brigham and Women's Hospital and Harvard, Medical School, Boston, MA 02115, USA.
Zhigang Li
Ha-Won Jeong
Matthew D Brown
David B Sacks
Harvard University · USBrigham and Women's Hospital · US

Funding

CALMODULIN IN NEOPLASTIC TRANSFORMATION OF BREAST TISSUER01CA075205 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKS, DAVID B · 1999 to 2008
$2.8M
NCI NIH HHS R01 CA075205
6 · The paper itself

Abstract

Cell migration, a highly complex physiological phenomenon that requires the co-ordinated and tightly regulated function of several proteins, is mediated by a number of signalling pathways. Elucidation of the molecular mechanisms of cell migration impacts our comprehension of numerous cell functions, ranging from development and immune surveillance to angiogenesis and metastasis. The scaffold protein IQGAP1, which binds multiple proteins and regulates their functions, promotes cell motility. Many of the IQGAP1 binding proteins have been implicated in cell migration. In this study, we employed a multifaceted strategy to identify proteins that contribute to IQGAP1-stimulated cell migration. Using specific IQGAP1 point mutant constructs, an interaction with actin was shown to be essential for IQGAP1 to increase cell migration. In contrast, eliminating the binding of Ca(2+)/calmodulin, but not Ca(2+)-free calmodulin, augmented the ability of IQGAP1 to stimulate cell migration. Consistent with these findings, selective inhibition of calmodulin function at the plasma membrane with a specific peptide inhibitor enhanced cell migration mediated by IQGAP1. Interestingly, immunofluorescence staining and confocal microscopy suggest that localization of Cdc42 at the leading edge is not necessary for maximal migration of epithelial cells. Coupled with the observations that Cdc42 and Rac1 contribute to IQGAP1-stimulated cell migration, these data suggest that IQGAP1 serves as a junction to integrate multiple signalling molecules to facilitate cell migration.

Indexed as

Cell MovementActinsCalmodulincdc42 GTP-Binding ProteinCell Line, TumorHumansProtein BindingProteinsrac1 GTP-Binding Proteinras GTPase-Activating ProteinsActinsCalmodulincdc42 GTP-Binding ProteinIQ motif containing GTPase activating protein 1Proteinsrac1 GTP-Binding Proteinras GTPase-Activating Proteins

Identifiers

PMID17544257
PMCPMC1992526
OpenAlexW1973572530

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.