Evidence map›Paper›PMID 41185006›Full record

ArticleBMC urology2025

NPRL2 gene expression as a predictor of biochemical recurrence after robot-assisted radical prostatectomy.

Sedat Yahsi, Pınar Öksüz, Kazım Ceviz, Cavit Ceylan

Abstract read
In one paragraph

Article in BMC urology, 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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1 · What the graph read from it

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2 · The registry

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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

4 authors.

Sedat YahsiDepartment of Urology, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-5641-3697
Pınar ÖksüzDepartment of Pathology, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-0334-2076
Kazım CevizDepartment of Urology, Ankara City Hospital, Ankara, Turkey. kazimmzz@hotmail.com.ORCID http://orcid.org/0000-0001-6343-383X
Cavit CeylanDepartment of Urology, Ankara City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-5159-1291

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to investigate the potential prognostic role of nitrogen permease regulator-like 2 (NPRL2) gene expression in predicting biochemical recurrence (BCR) following robot-assisted radical prostatectomy (RARP). MATERIALS AND

methodsThis single-center retrospective study included patients who underwent RARP performed by three different surgeons. Clinicopathological data and NPRL2 expression in tumor tissues were evaluated immunohistochemically (IHC). The level of NPRL2 staining was quantitatively assessed using an IHC score based on staining intensity. Factors associated with BCR were analyzed using multivariable logistic regression.

resultsA preoperative PSA level > 10 ng/mL (OR: 4.10, 95% CI: 1.38-12.20, p = 0.011), an International Society of Urological Pathology (ISUP) grade group > 3 (OR: 4.39, 95% CI: 1.45-13.29, p = 0.009), and high NPRL2 expression (IHC score > 4) (OR: 3.82, 95% CI: 1.07-13.62, p = 0.039) were identified as independent risk factors for BCR.

conclusionHigh NPRL2 expression is associated with an increased risk of BCR following RARP. These findings suggest a potential prognostic value of NPRL2; however, further validation studies are needed due to the small sample size and the subjective nature of the assessment. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Gene Expression Regulation, NeoplasticNeoplasm Recurrence, LocalProstatectomyProstatic NeoplasmsRobotic Surgical ProceduresAgedBiomarkers, TumorGene ExpressionHumansMaleMiddle AgedPredictive Value of TestsPrognosisProstate-Specific AntigenRetrospective StudiesBiomarkers, TumorProstate-Specific AntigenBiochemical recurrenceNPRL2 gene expressionProstate cancerRobot-assisted radical prostatectomy

Identifiers

PMID41185006
PMCPMC12581368

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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.