Evidence map›Paper›PMID 15952937›Full record

ArticleThe Biochemical journal2005

Participation of both Gab1 and Gab2 in the activation of the ERK/MAPK pathway by epidermal growth factor.

Songshu Meng, Zhengming Chen, Teresita Munoz-Antonia, Jie Wu

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

37 citing papers in PubMed, 82 citations in OpenAlex.

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  14. Cleavage of Grb2-Associated Binding Protein 2 by Viral Proteinase 2A duringFrontiers in cellular and infection microbiology · 2017
    Article
  15. Article
  16. Article
  17. CSF-1 receptor signaling in myeloid cells.Cold Spring Harbor perspectives in biology · 2014
    Review
  18. Article
  19. Article
  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 1 institution in 1 country.

Songshu MengMolecular Oncology Program, H. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Drive, Tampa, FL 33612, USA.
Zhengming Chen
Teresita Munoz-Antonia
Jie Wu
University of South Florida · US

Funding

Modulation of ErbB SignalingR01CA077467 · NCI · H. LEE MOFFITT CANCER CTR &RES INST · PI WU, JIE · 2003 to 2007
$1.4M
SIGNAL TRANSDUCTION BY LYSOPHOSPHATIDIC ACIDR29CA077467 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI WU, JIE · 1999 to 2003
$412k
Modulation of ErbB SignalingR56CA077467 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI WU, JIE · 2009 to 2009
$290k
NCI NIH HHS CA77467NCI NIH HHS R01 CA077467NCI NIH HHS R29 CA077467NCI NIH HHS R56 CA077467
6 · The paper itself

Abstract

Three members of Gab family docking proteins, Gab1, Gab2 and Gab3, have been identified in humans. Previous studies have found that the hepatocyte growth factor preferentially utilizes Gab1 for signalling, whereas Bcr-Abl selectively signals through Gab2. Gab1-SHP2 interaction has been shown to mediate ERK (extracellular-signal-regulated kinase) activation by EGF (epidermal growth factor). However, it was unclear whether EGF selectively utilizes Gab1 for signalling to ERK and whether Gab2 is dispensable in cells where Gab1 and Gab2 are co-expressed. Using T47D and MCF-7 human breast carcinoma cells that express endogenous Gab1 and Gab2, we examined the role of these docking proteins in EGF-induced ERK activation. It was found that EGF induced a similar amount of SHP2-Gab1 and SHP2-Gab2 complexes. Expression of either SHP2-binding defective Gab1 or Gab2 mutant blocked EGF-induced ERK activation. Down-regulation of either Gab1 or Gab2 by siRNAs (small interfering RNAs) effectively inhibited the EGF-stimulated ERK activation pathway and cell migration. Interestingly, the inhibitory effect of Gab1 siRNA could be rescued not only by expression of an exogenous mouse Gab1 but also by an exogenous human Gab2 and vice versa, but not by IRS1 (insulin receptor substrate 1). These results reveal that Gab2 plays a pivotal role in the EGF-induced ERK activation pathway and that it can complement the function of Gab1 in the EGF signalling pathway. Furthermore, Gab1 and Gab2 are critical signalling threshold proteins for ERK activation by EGF.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBase SequenceCell Line, TumorCell MovementChlorocebus aethiopsCOS CellsDown-RegulationEnzyme ActivationEpidermal Growth FactorExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, EnzymologicGene SilencingHumansIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase 1Adaptor Proteins, Signal TransducingEpidermal Growth FactorExtracellular Signal-Regulated MAP KinasesGAB1 protein, humanGAB2 protein, humanIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase 1PhosphoproteinsProtein Tyrosine Phosphatase, Non-Receptor Type 11Protein Tyrosine PhosphatasesPTPN11 protein, humanPtpn11 protein, mouseRNA, Small Interfering

Identifiers

PMID15952937
PMCPMC1237148
OpenAlexW1973415230

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.