Evidence map›Paper›PMID 30755582›Full record

ReviewExperimental & molecular medicine2019

PAK4 signaling in health and disease: defining the PAK4-CREB axis.

So-Yoon Won, Jung-Jin Park, Eun-Young Shin, Eung-Gook Kim

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

51 citing papers in PubMed, 86 citations in OpenAlex.

  1. Computational Identification of New Dual PAK4 and NAMPT Inhibitors.International journal of molecular sciences · 2026
    Article
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  5. Role of serine/threonine phosphatases 1 and 2A in pancreatic acinar fluid and electrolyte secretion.American journal of physiology. Gastrointestinal and liver physiology · 2026
    Article
  6. Article
  7. Review
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  9. Clinicopathological implications of miR-3127 in melanoma.Journal of pathology and translational medicine · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
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  15. p21-Activated Kinase 4 and Ischemic Acute Kidney Injury in Mice and Humans.Journal of the American Society of Nephrology : JASN · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Inhibition of NAMPT by PAK4 Inhibitors.International journal of molecular sciences · 2024
    Article
  20. Review
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.

So-Yoon WonDepartment of Biochemistry, Chungbuk National University College of Medicine, Cheongju, 28644, Korea.
Jung-Jin ParkDepartment of Biochemistry, Chungbuk National University College of Medicine, Cheongju, 28644, Korea.
Eun-Young Shin *Department of Biochemistry, Chungbuk National University College of Medicine, Cheongju, 28644, Korea. eyshin@chungbuk.ac.kr.
Eung-Gook Kim *Department of Biochemistry, Chungbuk National University College of Medicine, Cheongju, 28644, Korea. egkim@chungbuk.ac.kr.
Chungbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

p21-Activated kinase 4 (PAK4), a member of the PAK family, regulates a wide range of cellular functions, including cell adhesion, migration, proliferation, and survival. Dysregulation of its expression and activity thus contributes to the development of diverse pathological conditions. PAK4 plays a pivotal role in cancer progression by accelerating the epithelial-mesenchymal transition, invasion, and metastasis. Therefore, PAK4 is regarded as an attractive therapeutic target in diverse types of cancers, prompting the development of PAK4-specific inhibitors as anticancer drugs; however, these drugs have not yet been successful. PAK4 is essential for embryonic brain development and has a neuroprotective function. A long list of PAK4 effectors has been reported. Recently, the transcription factor CREB has emerged as a novel effector of PAK4. This finding has broad implications for the role of PAK4 in health and disease because CREB-mediated transcriptional reprogramming involves a wide range of genes. In this article, we review the PAK4 signaling pathways involved in prostate cancer, Parkinson's disease, and melanogenesis, focusing in particular on the PAK4-CREB axis.

Indexed as

Disease SusceptibilitySignal TransductionAnimalsCyclic AMP Response Element-Binding ProteinHumansMelaninsNeoplasmsp21-Activated KinasesParkinson DiseaseProtein BindingProtein Interaction Domains and MotifsCyclic AMP Response Element-Binding ProteinMelaninsp21-Activated KinasesPAK4 protein, human

Identifiers

PMID30755582
PMCPMC6372590
OpenAlexW2911929133

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.