Evidence map›Paper›PMID 20507214›Full record

ReviewExpert opinion on therapeutic targets2010

PAK1 as a therapeutic target.

Julia V Kichina, Anna Goc, Belal Al-Husein, Payaningal R Somanath, Eugene S Kandel

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

77 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Regulation of Cancer Metastasis by PAK2.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

17 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

5 authors at 4 institutions in 1 country.

Julia V KichinaRoswell Park Cancer Institute, Department of Cell Stress Biology, Elm and Carlton Streets, Buffalo, NY 14263, USA.
Anna Goc
Belal Al-Husein
Payaningal R Somanath
Eugene S Kandel
Augusta University · USRoswell Park Comprehensive Cancer Center · USUniversity of Georgia · USWeatherford College · US

Funding

Genetic Determinants of Akt-induced TransformationK01CA098176 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI KANDEL, EUGENE S · 2005 to 2009
$641k
REVERSIBLE PROMOTER-INSERTION FOR IN VIVO STUDIES OF MELANOMAR21CA116060 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI KANDEL, EUGENE S · 2005 to 2006
$253k
NCI NIH HHS CA098176NCI NIH HHS CA116060NCI NIH HHS CA1337708NCI NIH HHS K01 CA098176NCI NIH HHS R21 CA116060
6 · The paper itself

Abstract

importance of the fieldP21-activated kinases (PAKs) are involved in multiple signal transduction pathways in mammalian cells. PAKs, and PAK1 in particular, play a role in such disorders as cancer, mental retardation and allergy. Cell motility, survival and proliferation, the organization and function of cytoskeleton and extracellular matrix, transcription and translation are among the processes affected by PAK1. AREAS COVERED IN THIS REVIEW: We discuss the mechanisms that control PAK1 activity, its involvement in physiological and pathophysiological processes, the benefits and the drawbacks of the current tools to regulate PAK1 activity, the evidence that suggests PAK1 as a therapeutic target and the likely directions of future research. WHAT THE READER WILL GAIN: The reader will gain a better knowledge and understanding of the areas described above. TAKE HOME MESSAGE: PAK1 is a promising therapeutic target in cancer and allergen-induced disorders. Its suitability as a target in vascular, neurological and infectious diseases remains ambiguous. Further advancement of this field requires progress on such issues as the development of specific and clinically acceptable inhibitors, the choice between targeting one or multiple PAK isoforms, elucidation of the individual roles of PAK1 targets and the mechanisms that may circumvent inhibition of PAK1.

Indexed as

AnimalsEnzyme ActivationGene Expression Regulation, EnzymologicHumansHypersensitivityImmunityIntellectual DisabilityIsoenzymesNeoplasmsOrgan Specificityp21-Activated KinasesProtein Structure, TertiarySignal TransductionSubstrate SpecificityIsoenzymesp21-Activated KinasesPAK1 protein, human

Identifiers

PMID20507214
PMCPMC3137287
OpenAlexW2061709289

What OpenQuestion holds

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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.