Evidence map›Paper›PMID 25247494›Full record

ArticlePloS one2014

PTEN redundancy: overexpressing lpten, a homolog of Dictyostelium discoideum ptenA, the ortholog of human PTEN, rescues all behavioral defects of the mutant ptenA-.

Daniel F Lusche, Deborah Wessels, Nicole A Richardson, Kanoe B Russell, Brett M Hanson, Benjamin A Soll, Benjamin H Lin, David R Soll

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Actin Waves and Dynamic Patterning of the Plasma Membrane.The Yale journal of biology and medicine · 2019
    Article
  2. OverexpressingOncotarget · 2018
    Article
  3. 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

8 authors at 2 institutions in 1 country.

Daniel F LuscheMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Deborah WesselsMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Nicole A RichardsonMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Kanoe B RussellMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Brett M HansonMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Benjamin A SollMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Benjamin H LinMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
David R SollMonoclonal Antibody Research Institute and Developmental Studies Hybridoma Bank, Department of Biology, The University of Iowa, Iowa City, Iowa, United States of America.
Developmental Studies Hybridoma Bank · USUniversity of Iowa · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the tumor suppressor gene PTEN are associated with a significant proportion of human cancers. Because the human genome also contains several homologs of PTEN, we considered the hypothesis that if a homolog, functionally redundant with PTEN, can be overexpressed, it may rescue the defects of a PTEN mutant. We have performed an initial test of this hypothesis in the model system Dictyostelium discoideum, which contains an ortholog of human PTEN, ptenA. Deletion of ptenA results in defects in motility, chemotaxis, aggregation and multicellular morphogenesis. D. discoideum also contains lpten, a newly discovered homolog of ptenA. Overexpressing lpten completely rescues all developmental and behavioral defects of the D. discoideum mutant ptenA-. This hypothesis must now be tested in human cells.

Indexed as

Base SequenceChemotaxisCyclic AMPDictyosteliumDNA, ProtozoanGene Knockout TechniquesGenes, ProtozoanHumansMolecular Sequence DataProtein Structure, TertiaryProtozoan ProteinsPTEN PhosphohydrolaseRecombinant Fusion ProteinsSpecies SpecificityCyclic AMPDNA, ProtozoanProtozoan ProteinsPTEN PhosphohydrolasePTEN protein, humanRecombinant Fusion Proteins

Identifiers

PMID25247494
PMCPMC4172592
OpenAlexW2010721257

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.