Evidence map›Paper›PMID 17202406›Full record

ArticleMolecular biology of the cell2007

Loss of Vav2 proto-oncogene causes tachycardia and cardiovascular disease in mice.

Vincent Sauzeau, Mirjana Jerkic, José M López-Novoa, Xosé R Bustelo

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

46 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
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  3. Article
  4. RAC1 signaling in prostate cancer: VAV GEFs take center stage.Frontiers in cell and developmental biology · 2025
    Article
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  15. International journal of environmental research and public health · 2020
    Article
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  18. 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

4 authors at 2 institutions in 1 country.

Vincent SauzeauCentro de Investigación del Cáncer, Instituto de Biología Molecular y Celular del Cáncer, University of Salamanca, E-37007 Salamanca, Spain.
Mirjana Jerkic
José M López-Novoa
Xosé R Bustelo
Centro de Investigación del Cáncer · ESConsejo Superior de Investigaciones Científicas · ES

Funding

VAV FAMILY PROTEINS IN CELL SIGNALING AND CANCERR01CA073735 · NCI · UNIVERSITY OF SALAMANCA · PI BUSTELO, XOSE R · 1997 to 2009
$1.8M
NCI NIH HHS R01 CA073735NCI NIH HHS R01-CA73735-09
6 · The paper itself

Abstract

The Vav family is a group of signal transduction molecules that activate Rho/Rac GTPases during cell signaling. Experiments using knockout mice have indicated that the three Vav proteins present in mammals (Vav1, Vav2, and Vav3) are essential for proper signaling responses in hematopoietic cells. However, Vav2 and Vav3 are also highly expressed in nonhematopoietic tissues, suggesting that they may have additional functions outside blood cells. Here, we report that this is the case for Vav2, because the disruption of its locus in mice causes tachycardia, hypertension, and defects in the heart, arterial walls, and kidneys. We also provide physiological and pharmacological evidence demonstrating that the hypertensive condition of Vav2-deficient mice is due to a chronic stimulation of the renin/angiotensin II and sympathetic nervous systems. Together, these results indicate that Vav2 plays crucial roles in the maintenance of cardiovascular homeostasis in mice.

Indexed as

Adrenal GlandsAldosteroneAnimalsAortaEndothelinsGene Expression RegulationGuanine Nucleotide Exchange FactorsHeart VentriclesHypertensionKidneyKidney Function TestsMiceMice, KnockoutPhenotypeProto-Oncogene Proteins c-vavRenin-Angiotensin SystemAldosteroneEndothelinsGuanine Nucleotide Exchange FactorsProto-Oncogene Proteins c-vavVasopressinsVav2 protein, mouseVav3 protein, mouse

Identifiers

PMID17202406
PMCPMC1805112
OpenAlexW2121398382

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.