Evidence map›Paper›PMID 41112831›Full record

ArticleOncology letters2025

FBXL22, a circadian-regulated immune biomarker with pan-cancer prognostic value and therapeutic potential in prostate cancer.

Jin Liu, Maoyuan Feng, Jian Zhou, Shijie Yang, Yue Shi, Wenping Li

Abstract read
In one paragraph

Article in Oncology letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jin LiuDepartment of Urology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Maoyuan FengDepartment of Urology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Jian ZhouDepartment of Urology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Shijie YangDepartment of Urology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei 050051, P.R. China.
Yue ShiChina National Center for Bioinformation, Beijing 100101, P.R. China.
Wenping LiDepartment of Urology, Hebei Medical University Third Hospital, Shijiazhuang, Hebei 050051, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

F-box and leucine-rich repeat protein 22 (FBXL22) has been implicated in breast and prostate cancer types; however, comprehensive pan-cancer analyses and detailed investigations of its role in cancer development are still needed. To address this, the present study used The Cancer Genome Atlas, Genotype-Tissue Expression, University of ALabama at Birmingham CANcer data analysis Portal, Kaplan-Meier-Plotter and cBioPortal databases to analyze the correlation between FBXL22 expression and prognosis, gene mutations, DNA methylation, immune cell infiltration and immune-related gene regulation in several types of cancer. The findings of the present study demonstrated that FBXL22 was predominantly downregulated in several cancer types and may serve as a prognostic and diagnostic marker in certain cancer types, particularly prostate cancer. Strong correlations between FBXL22 expression and immune checkpoint genes were observed, which suggests a role in the tumor immune microenvironment. Additionally, FBXL22 expression was associated with infiltration of cancer-associated fibroblasts and endothelial cells, which may affect immunotherapy outcomes. Mechanistically, FBXL22 was involved in circadian rhythm regulation, ubiquitin-mediated proteolysis, focal adhesion signaling and cGMP-protein kinase G signaling. In prostate cancer, FBXL22 upregulation suppressed cell viability, invasion and metastasis, while promoting apoptosis, potentially through modulation of the polo-like kinase 1 pathway. To the best of our knowledge, the present study provides the first comprehensive pan-cancer analysis of FBXL22, which highlights its potential as an immune biomarker and therapeutic target for multiple cancer types with implications for precision medicine.

Indexed as

biomarkersF-box and leucine-rich repeat protein 22pan-cancerprostate cancertumor immune microenvironment

Identifiers

PMID41112831
PMCPMC12531760

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