Evidence map›Paper›PMID 41570183›Full record

ArticleThe Prostate2026

Evaluation of Loss of the Y Chromosome in Peripheral Blood as a Biomarker for Prostate Cancer.

Jun Lu, Yan Lu, Takuro Kobayashi, Tsuyoshi Hachiya, Haruhiko Wakita, Yiming Jin, Yasunari Tanaka, Yoshihiro Ikehata, Masayoshi Nagata, Hisamitsu Ide and 1 more

Abstract read
In one paragraph

Article in The Prostate, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Jun LuDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0009-0007-0218-5263
Yan LuDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Takuro KobayashiDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3141-7226
Tsuyoshi HachiyaData Science and Informatics for Genetic Disorders, Graduate School of Medicine, Juntendo University, Tokyo, Japan.ORCID https://orcid.org/0000-0002-5274-3266
Haruhiko WakitaDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Yiming JinDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Yasunari TanakaDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Yoshihiro IkehataDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Masayoshi NagataDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Hisamitsu IdeDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.
Shigeo HorieDepartment of Urology, Juntendo University, Graduate School of Medicine, Tokyo, Japan.

Funding

KAKENHI (Grants-in-Aid for Scientific Research) from the Japan Society for the Promotion of Science (JSPS) 24K12476
6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is the most common malignant tumor in men, but the widely used prostate-specific antigen (PSA) test has limited diagnostic accuracy. Research proposes that the loss of the Y chromosome (LOY) may affect the occurrence and development of prostate cancer, aiming to assess its potential as a diagnostic biomarker to improve the accuracy of prostate cancer detection and clinical management.

methodsLOY levels were measured using droplet digital polymerase chain reaction (ddPCR) method, integrating relevant clinical indicators to evaluate the potential clinical significance of LOY in PCa. Logistic regression was employed to estimate risk prediction capability of LOY, and model performance was validated through bootstrapping.

findings131 men patients were enrolled in this study whose PSA level exceeding 4.0 ng/ml and underwent prostate biopsies. According to post-biopsy pathological results, subjects were classified into normal and cancer groups. LOY levels were significantly higher in the cancer group than in the normal group (p < 0.001). LOY levels show a consistent increase with advancing AJCC clinical stage and escalating PI-RADS scores. LOY is a promising biomarker for PCa (AUC = 0.898). Clinical decision curve analyzes demonstrated that incorporating LOY into each conventional model provided greater clinical benefit compared with the original model.

interpretationIn biopsy patients, the LOY levels in the cancer group were higher than those in the normal group, and this was more pronounced in patients at advanced clinical stages. LOY levels have strong diagnostic efficacy for PCa, indicating that LOY may serve as an auxiliary biomarker for early PCa diagnosis.

Indexed as

Biomarkers, TumorChromosomes, Human, YProstatic NeoplasmsAgedBiopsyHumansMaleMiddle AgedProstate-Specific AntigenBiomarkers, TumorProstate-Specific AntigenbiomarkersdiagnosisLOYprostate cancerPSA

Identifiers

PMID41570183
PMCPMC13034021

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.