Evidence map›Paper›PMID 20534451›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

Pseudopodium-enriched atypical kinase 1 regulates the cytoskeleton and cancer progression [corrected].

Yingchun Wang, Jonathan A Kelber, Hop S Tran Cao, Greg T Cantin, Rui Lin, Wei Wang, Sharmeela Kaushal, Jeanne M Bristow, Thomas S Edgington, Robert M Hoffman and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

76 citing papers in PubMed, 118 citations in OpenAlex.

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Yingchun WangDepartment of Pathology, Moores Cancer Center, University of California, La Jolla, CA 92093, USA.
Jonathan A Kelber
Hop S Tran Cao
Greg T Cantin
Rui Lin
Wei Wang
Sharmeela Kaushal
Jeanne M Bristow
Thomas S Edgington
Robert M Hoffman
Michael Bouvet
John R Yates
Richard L Klemke
Moores Cancer CenterScripps Research Institute · USSociety of Surgical Oncology · USUniversity of California, San Diego · US

Funding

STRUCTUREU54GM064346 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI IMPERIALI, BARBARA · 2001 to 2010
$74.9M
UCSD Cancer Center Training Program in Drug DevelopmentT32CA121938 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Michael Bouvet, Dwayne G. Stupack · 2006 to 2026
$10.3M
Survival Mechanisms of Invasive Carcinoma CellsR01CA097022 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KLEMKE, RICHARD L. · 2003 to 2017
$4.6M
Mechanisms of Lamellipodia Growth &RetractionR01GM068487 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KLEMKE, RICHARD L. · 2003 to 2011
$2.3M
NCI NIH HHS CA097022NCI NIH HHS R01 CA097022NCI NIH HHS T32 CA121938NIGMS NIH HHS GM064346NIGMS NIH HHS GM068487NIGMS NIH HHS R01 GM068487NIGMS NIH HHS U54 GM064346
6 · The paper itself

Abstract

Regulation of the actin-myosin cytoskeleton plays a central role in cell migration and cancer progression. Here, we report the discovery of a cytoskeleton-associated kinase, pseudopodium-enriched atypical kinase 1 (PEAK1). PEAK1 is a 190-kDa nonreceptor tyrosine kinase that localizes to actin filaments and focal adhesions. PEAK1 undergoes Src-induced tyrosine phosphorylation, regulates the p130Cas-Crk-paxillin and Erk signaling pathways, and operates downstream of integrin and epidermal growth factor receptors (EGFR) to control cell spreading, migration, and proliferation. Perturbation of PEAK1 levels in cancer cells alters anchorage-independent growth and tumor progression in mice. Notably, primary and metastatic samples from colon cancer patients display amplified PEAK1 levels in 81% of the cases. Our findings indicate that PEAK1 is an important cytoskeletal regulatory kinase and possible target for anticancer therapy.

Indexed as

ActinsAnimalsBase SequenceCell LineCell Line, TumorCell MovementCell ProliferationColonic NeoplasmsComputational BiologyCytoskeletonDNA PrimersFemaleFocal AdhesionsHumansIn Vitro TechniquesLiver NeoplasmsActinsDNA PrimersPhosphotyrosineProtein-Tyrosine KinasesRecombinant Fusion Proteinssrc-Family Kinases

Identifiers

PMID20534451
PMCPMC2890752
OpenAlexW1989686918

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.