Evidence map›Paper›PMID 16456542›Full record

ArticleThe EMBO journal2006

PTEN tumor suppressor associates with NHERF proteins to attenuate PDGF receptor signaling.

Yoko Takahashi, Fabiana C Morales, Erica L Kreimann, Maria-Magdalena Georgescu

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The EMBO journal, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

118 citing papers in PubMed, 220 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Concurrent PTEN and PDGFRB Alterations Characterize Storiform Collagenoma.The American journal of surgical pathology · 2024
    Article
  6. Article
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  8. Review
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  16. A Critical Role for NaJournal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  17. PHLPPing the Script: Emerging Roles of PHLPP Phosphatases in Cell Signaling.Annual review of pharmacology and toxicology · 2021
    Review
  18. Article
  19. Article
  20. Article

58 more citing papers are in PubMed but not listed here.

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.

Yoko TakahashiDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Fabiana C Morales
Erica L Kreimann
Maria-Magdalena Georgescu
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
TRAINING PROGRAM IN MOLECULAR GENETICS OF CANCERT32CA009299 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOZANO, GUILLERMINA · 1985 to 2014
$4.7M
Connecting PTEN and NF2 cancer predisposition syndromesR01CA107201 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GEORGESCU, MARIA-MAGDALENA · 2005 to 2009
$1.6M
NCI NIH HHS CA09299-26NCI NIH HHS CA107201NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA107201NCI NIH HHS T32 CA009299
6 · The paper itself

Abstract

PTEN, a tumor suppressor frequently inactivated in many human cancers, directly antagonizes the activity of phosphatidylinositol-3-OH kinase (PI3K) by dephosphorylating phosphoinositides. We show here that PTEN interacts directly with the NHERF1 and NHERF2 (Na+/H+ exchanger regulatory factor) homologous adaptor proteins through the PDZ motif of PTEN and the PDZ1 domain of NHERF1 or both PDZ domains of NHERF2. NHERFs were shown to interact directly with platelet-derived growth factor receptor (PDGFR), and we demonstrate the assembly of a ternary complex between PTEN, NHERFs and PDGFR. The activation of the PI3K pathway after PDGFR stimulation was prolonged in NHERF1(-/-) mouse embryonic fibroblasts as compared to wild-type cells, consistent with defective PTEN recruitment to PDGFR in the absence of NHERF1. Depletion of NHERF2 by small interfering RNA similarly increased PI3K signaling. Phenotypically, the loss of NHERF1 enhanced the PDGF-induced cytoskeletal rearrangements and chemotactic migration of the cells. These data indicate that, in normal cells, NHERF proteins recruit PTEN to PDGFR to restrict the activation of the PI3K.

Indexed as

AnimalsCell Line, TumorChemotaxisCytoskeletonEnzyme ActivationFibroblastsHumansMicePhosphatidylinositol 3-KinasesPhosphoproteinsPlatelet-Derived Growth FactorPTEN PhosphohydrolaseReceptors, Platelet-Derived Growth FactorSodium-Hydrogen ExchangersPhosphatidylinositol 3-KinasesPhosphoproteinsPlatelet-Derived Growth FactorPTEN PhosphohydrolasePTEN protein, humanPten protein, mouseReceptors, Platelet-Derived Growth Factorsodium-hydrogen exchanger regulatory factorSodium-Hydrogen Exchangers

Identifiers

PMID16456542
PMCPMC1383560
OpenAlexW2083879234

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.