Evidence map›Paper›PMID 40746562›Full record

ArticleFrontiers in immunology2025

PCP4 inhibits the progression of prostate cancer through Ca

Wenqiao Jia, Zeyuan Yu, Feifei Sun, Ping Liu, Bo Han

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Wenqiao JiaDepartment of Health Management Center, Qilu Hospital of Shandong University, Jinan, China.
Zeyuan YuThe Key Laboratory of Experimental Teratology, Ministry of Education and Department of Pathology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China.
Feifei SunDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, China.
Ping LiuThe Key Laboratory of Experimental Teratology, Ministry of Education and Department of Pathology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China.
Bo HanDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The development of prostate cancer (PCa) remains a major health threat for men worldwide. Calcium/Calmodulin signaling pathway has been implicated to the initiation and progression of diverse human cancers. Loss or downregulation of Purkinje cell protein 4 (PCP4), is frequently observed in some prostate cancer patients, particularly those with castration-resistant prostate cancer (CRPC). Methods: Public datasets were used to analyze PCP4 expression and the relationship between PCP4 expression and clinicopathological characteristics of PCa patients. Gain- and loss-of-function studies in PCa cell lines and mouse models were performed to characterize the role of PCP4 in tumor progression. A series of molecular and biochemical experiments were carried out in PCa cell lines to investigate the mechanism underlying PCP4-mediated tumor suppression. Results: (1) Conclusion: Our findings elucidate the molecular mechanism that PCP4 downregulation promotes PCa progression via Ca

Indexed as

AMP-Activated Protein KinasesCalciumCalcium-Calmodulin-Dependent Protein Kinase KinaseNerve Tissue ProteinsProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantReceptors, AndrogenAnimalsCell Line, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansMaleMiceSignal TransductionAMP-Activated Protein KinasesAR protein, humanCalciumCalcium-Calmodulin-Dependent Protein Kinase KinaseCAMKK2 protein, humanNerve Tissue ProteinsReceptors, AndrogenCRPCPCP4PEP-19progressionprostate cancer

Identifiers

PMID40746562
PMCPMC12311239

What Socratic holds

Textmetadata
LicenceCC BY
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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.