Evidence map›Paper›PMID 20808771›Full record

ArticlePloS one2010

Dcas supports cell polarization and cell-cell adhesion complexes in development.

Nadezhda Tikhmyanova, Alexei V Tulin, Fabrice Roegiers, Erica A Golemis

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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  8. Nedd9 restrains renal cystogenesis in Pkd1-/- mice.Proceedings of the National Academy of Sciences of the United States of America · 2014
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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.

Nadezhda TikhmyanovaFox Chase Cancer Center, Philadelphia, Pennsylvania, United States of America.
Alexei V Tulin
Fabrice Roegiers
Erica A Golemis
Fox Chase Cancer Center · USDrexel University · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
ROLES OF HEF1 IN CELL DIFFERENTIATION AND SURVIVALR01CA063366 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GOLEMIS, ERICA A. · 1998 to 2013
$3.9M
Endocytic Control of Notch-Mediated Cell Fate Decisions in NeurogenesisR01NS059971 · NINDS · RESEARCH INST OF FOX CHASE CAN CTR · PI ROEGIERS, FABRICE J. · 2008 to 2012
$1.7M
Poly ADP-ribose Polymerase in Chromatin and Transcriptional RegulationR01GM077452 · NIGMS · RESEARCH INST OF FOX CHASE CAN CTR · PI TULIN, ALEXEI V · 2008 to 2012
$1.6M
Cas Protein Regulation of EMT in CancerR01CA113342 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GOLEMIS, ERICA A. · 2007 to 2011
$1.5M
CONTROL OF NORMAL AND ABNORMAL CELL GROWTHR29CA063366 · NCI · INSTITUTE FOR CANCER RESEARCH · PI GOLEMIS, ERICA A · 1994 to 1997
–
NCI NIH HHS CA06927NCI NIH HHS CA113342NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA063366NCI NIH HHS R01 CA113342NCI NIH HHS R01S CA63366NIGMS NIH HHS R01 GM077452NINDS NIH HHS R01 NS059971
6 · The paper itself

Abstract

Mammalian Cas proteins regulate cell migration, division and survival, and are often deregulated in cancer. However, the presence of four paralogous Cas family members in mammals (BCAR1/p130Cas, EFS/Sin1, NEDD9/HEF1/Cas-L, and CASS4/HEPL) has limited their analysis in development. We deleted the single Drosophila Cas gene, Dcas, to probe the developmental function of Dcas. Loss of Dcas had limited effect on embryonal development. However, we found that Dcas is an important modulator of the severity of the developmental phenotypes of mutations affecting integrins (If and mew) and their downstream effectors Fak56D or Src42A. Strikingly, embryonic lethal Fak56D-Dcas double mutant embryos had extensive cell polarity defects, including mislocalization and reduced expression of E-cadherin. Further genetic analysis established that loss of Dcas modified the embryonal lethal phenotypes of embryos with mutations in E-cadherin (Shg) or its signaling partners p120- and beta-catenin (Arm). These results support an important role for Cas proteins in cell-cell adhesion signaling in development.

Indexed as

Cell PolarityAllelesAnimalsCadherinsCell AdhesionCytoskeletonDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEpithelial CellsFemaleGene DeletionIntegrinsIntercellular JunctionsMaleMesodermCadherinscas protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsIntegrins

Identifiers

PMID20808771
PMCPMC2927436
OpenAlexW2026306905

What OpenQuestion 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 OpenQuestion graph.