Evidence map›Paper›PMID 38779687›Full record

ArticleFrontiers in immunology2024

IL-38 promotes the development of prostate cancer.

Huiyan Wu, Jing Yang, Liuhong Yuan, Zhenyu Tan, Xiuqin Zhang, Brett D Hambly, Shisan Bao, Kun Tao

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

8 citing papers in PubMed.

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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

8 authors.

Huiyan WuDepartment of Pathology, Tongji Hospital, Tongji University, Shanghai, China.
Jing YangDepartment of Pathology, Tongren Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Liuhong YuanDepartment of Pathology, Tongji Hospital, Tongji University, Shanghai, China.
Zhenyu TanDepartment of Pathology, Tongji Hospital, Tongji University, Shanghai, China.
Xiuqin ZhangDepartment of Pathology, Tongji Hospital, Tongji University, Shanghai, China.
Brett D HamblyDepartment of Pathology, Tongren Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Shisan BaoDepartment of Pathology, Tongren Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Kun TaoDepartment of Pathology, Tongji Hospital, Tongji University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Prostate Cancer (PCa) remains a significant concern in male cancer-related mortality. Tumour development is intricately regulated by the complex interactions between tumour cells and their microenvironment, making it essential to determine which is/are key factor(s) that influence the progression of PCa within the tumour microenvironment. Materials and methods: The current study utilised histopathology and immunohistochemistry to determine the expression of IL-38 in PCa and analysed the correlation between the expression level of IL-38 within PCa and clinical pathological characteristics. Results: There was a significant increase in IL-38 expression in PCa tissues compared to adjacent non-PCa tissues (P < 0.0001). In addition, IL-38 expression was significantly higher in tumour cells with a high proliferation index compared to those with a low value-added index. ROC curve analysis demonstrated that IL-38 has high specificity and sensitivity for the diagnosis of PCa (AUC=0.76). Moreover, we Probed the cellular source of IL-38 in prostate cancer tissue by immunofluorescence double staining. Additionally, within PCa, the expression of IL-38 was inversely correlated with the expression levels of CD8 and PD-1. Survival analysis revealed a significantly lower overall survival rate for PCa patients with high IL-38 expression (P=0.0069), and when IL-38 was co-expressed with CD8, the survival rate of the IL-38 Conclusion: These findings suggest that IL-38 plays a crucial role in the development of PCa, and the exploration of the correlation between IL-38 and various immune factors in the tumour microenvironment further reveals its mechanism of action, making it a potential target for immunotherapy in PCa.

Indexed as

InterleukinsProstatic NeoplasmsAgedBiomarkers, TumorHumansMaleMiddle AgedPrognosisProgrammed Cell Death 1 ReceptorTumor MicroenvironmentBiomarkers, TumorIL-38 protein, humanInterleukinsProgrammed Cell Death 1 ReceptorCD4CD8IL-38PD-1prognosisprostate cancer

Identifiers

PMID38779687
PMCPMC11109393

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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 OpenQuestion graph.