Evidence map›Paper›PMID 39756822›Full record

ArticlePhysiological reports2025

Genome analysis uncovers an inverse correlation between alterations in P21-activated kinases and patient survival across multiple cancer types.

Jessie M Vo, Linh M La, Ananda V Anderson, Abdulaziz H Alanazi, Payaningal R Somanath

Abstract read
In one paragraph

Article in Physiological reports, 2025. 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
–field-weighted citation impact
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.

  1. Article
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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

5 authors.

Jessie M VoClinical and Experimental Therapeutics, University of Georgia, Augusta, Georgia, USA.
Linh M LaClinical and Experimental Therapeutics, University of Georgia, Augusta, Georgia, USA.
Ananda V AndersonClinical and Experimental Therapeutics, University of Georgia, Augusta, Georgia, USA.
Abdulaziz H AlanaziClinical and Experimental Therapeutics, University of Georgia, Augusta, Georgia, USA.
Payaningal R SomanathClinical and Experimental Therapeutics, University of Georgia, Augusta, Georgia, USA.ORCID https://orcid.org/0000-0003-3017-0230

Funding

Implementing a Maternal health and PRegnancy Outcomes Vision for Everyone (IMPROVE)UL1TR002378 · NCATS · EMORY UNIVERSITY · PI Andres J Garcia, Elizabeth O. Ofili · 2017 to 2026
$92.1M
HHS | NIH | National Center for Advancing Translational Sciences (NCATS) UL1TR002378NCATS NIH HHS UL1 TR002378
6 · The paper itself

Abstract

Cancer is a complex disease with profound societal and economic impacts, especially in metastatic cases where treatment challenges arise due to the absence of reliable biomarkers and effective therapies. While P21-activated kinases (PAKs) play a key role in cancer progression, their potential as predictive markers for metastasis and therapeutic targets has not been fully explored. We hypothesized that genetic alterations in PAK isoforms could be linked to reduced overall patient survival. To investigate this, we used data from the cBioPortal for Cancer Genomics, analyzing several randomized, multicentered phase-3 clinical trial datasets. The analysis revealed significant genetic alterations in PAK genes, particularly in cancers such as breast, prostate, pancreatic, and lung. Notably, elevated PAK expression was associated with poorer survival outcomes in prostate and breast cancer patients. In pancreatic and lung cancers, although a trend of poorer survival with PAK alterations was observed, it was not statistically significant. Our findings underscore the importance of PAK isoforms as potential biomarkers and therapeutic targets, particularly in metastatic cancers. Further research could lead to improved patient outcomes through targeted interventions aimed at PAK-related pathways, with PAK serving as a reliable biomarker for the precise diagnosis, monitoring, and personalization of treatment strategies.

Indexed as

Neoplasmsp21-Activated KinasesBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleBiomarkers, Tumorp21-Activated Kinasescancergenetic alterationsmetastasisP21 activated kinasepatient survival

Identifiers

PMID39756822
PMCPMC11702381

What Socratic holds

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LicenceCC BY
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Registered trials

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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.