Evidence map›Paper›PMID 38993566›Full record

ArticleInternational journal of biological sciences2024

P2X7R Modulates NEK7-NLRP3 Interaction to Exacerbate Experimental Autoimmune Prostatitis via GSDMD-mediated Prostate Epithelial Cell Pyroptosis.

Lei Chen, Yi Liu, Shaoyu Yue, Hui Wang, Jia Chen, Wenming Ma, Wenlong Xu, Muyang Xu, Ziqi Chen, Xianguo Chen and 2 more

Abstract read
In one paragraph

Article in International journal of biological sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  18. Frontiers in immunology · 2025
    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

12 authors.

Lei ChenDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yi LiuDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Shaoyu YueDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Hui WangDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Jia ChenDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Wenming MaDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Wenlong XuDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Muyang XuDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Ziqi ChenDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Xianguo ChenDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Li ZhangDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Chaozhao LiangDepartment of Urology, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic prostatitis is one of the most common urologic diseases that troubles young men, with unclear etiology and ineffective treatment approach. Pyroptosis is a novel model of cell death, and its roles in chronic prostatitis are unknown. In this study, P2X7R, NEK7, and GSDMD-NT expression levels were detected in prostate tissues from benign prostate hyperplasia (BPH) patients and experiment autoimmune prostatitis (EAP) mice. P2X7R agonist, antagonist, NLRP3 inhibitor, and disulfiram were used to explore the roles of the P2X7R-NEK7-NLRP3 axis in prostate epithelial cell pyroptosis and chronic prostatitis development. We found that P2X7R, NEK7, and GSDMD-NT were highly expressed in the prostate epithelial cells of BPH patients with prostatic inflammation and EAP mice. Activation of P2X7R exacerbated prostatic inflammation and increased NLRP3 inflammasome component expressions and T helper 17 (Th17) cell proportion. Moreover, P2X7R-mediated potassium efflux promoted NEK7-NLRP3 interaction, and NLRP3 assembly and activation, which caused GSDMD-NT-mediated prostate epithelial cell pyroptosis to exacerbate EAP development. Disulfiram could effectively improve EAP by inhibiting GSDMD-NT-mediated prostate epithelial cell pyroptosis. In conclusion, the P2X7R-NEK7-NLRP3 axis could promote GSDMD-NT-mediated prostate epithelial cell pyroptosis and chronic prostatitis development, and disulfiram may be an effective drug to treat chronic prostatitis.

Indexed as

Epithelial CellsNIMA-Related KinasesNLR Family, Pyrin Domain-Containing 3 ProteinPhosphate-Binding ProteinsProstateProstatitisPyroptosisAnimalsAutoimmune DiseasesGasderminsHumansMaleMiceMice, Inbred C57BLPoly-ADP-Ribose Binding ProteinsReceptors, Purinergic P2X7GasderminsGSDMD protein, humanGsdmd protein, mouseNEK7 protein, humanNek7 protein, mouseNIMA-Related KinasesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNlrp3 protein, mouseP2RX7 protein, humanP2rx7 protein, mousePhosphate-Binding ProteinsPoly-ADP-Ribose Binding ProteinsReceptors, Purinergic P2X7Chronic prostatitis, Prostate epithelial cellDisulfiramP2X7RPyroptosis

Identifiers

PMID38993566
PMCPMC11234205

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.