Evidence map›Paper›PMID 40225987›Full record

ArticleAmerican journal of translational research2025

Upregulated PXDNL promotes invasive breast carcinoma progression.

Xianping Zhou, Yanqiu Zhang, Baoyu Huang, Xiufang Shi, Maohong Bian

Abstract read
In one paragraph

Article in American journal of translational research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xianping ZhouDepartment of Blood Transfusion, The First Affiliated Hospital of Anhui Medical University Hefei, Anhui, The People's Republic of China.
Yanqiu ZhangInstitute of Clinical Pharmacology, Anhui Medical University, Key Laboratory of Anti-inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-inflammatory and Immune Medicine Hefei, Anhui, The People's Republic of China.
Baoyu HuangDepartment of Gastrointestinal Surgery, The People's Hospital of Bozhou Bozhou, Anhui, The People's Republic of China.
Xiufang ShiDepartment of Clinical Laboratory, The People's Hospital of Bozhou Bozhou, Anhui, The People's Republic of China.
Maohong BianDepartment of Blood Transfusion, The First Affiliated Hospital of Anhui Medical University Hefei, Anhui, The People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInvasive breast carcinoma (BRCA) is a common and serious malignancy in women. Peroxidase-like (PXDNL) is associated with poor prognosis in various cancers but has an unclear role in BRCA progression.

methodsBioinformatic analysis of datasets from The Cancer Genome Atlas (TCGA), Genotype-Tissue Expression (GTEx), and UALCAN investigated a potential carcinogenic role of PXDNL, focusing on its correlation with prognosis, promoter methylation, immune cell infiltration, immune checkpoint genes, and relevant biologic functions and pathways.

resultsPXDNL demonstrated a significant expression profile in BRCA, with considerable diagnostic and prognostic implications. Its up-regulation correlated with decreased survival rates across various molecular subtypes of BRCA. Patients in the high PXDNL expression group showed reduced presence of multiple infiltrative immune cell types, including CD8+ T cells, cytotoxic cells, T cells, B cells, dendritic cells (DC), immature dendritic cells (iDC), natural killer (NK) cells, NK CD56bright cells, NK CD56dim cells, and follicular helper T cells (TFH). Additionally, a significant correlation was observed between PXDNL expression and immune checkpoint genes. Gene Set Enrichment Analysis (GSEA) further indicated that high PXDNL expression triggers pathways such as epithelial-mesenchymal transition and protein secretion, while suppressing crucial processes including allograft rejection, IL6-JAK-STAT3 signaling, TNFα signaling via NFκB, adipogenesis, oxidative phosphorylation, DNA repair, and the P53 pathway.

conclusionOverexpression of PXDNL is associated with poor prognosis and is linked to immune cell infiltration in BRCA. Thus, PXDNL may be a biomarker or therapeutic target for BRCA.

Indexed as

Breast invasive carcinomaimmune checkpointsimmune infiltrationprognosisPXDNL

Identifiers

PMID40225987
PMCPMC11982889

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