Evidence map›Paper›PMID 40760471›Full record

SynthesisBMC cancer2025

The research progress on diagnostic indicators related to prostate-specific antigen gray-zone prostate cancer.

Yeasin Ahamed, Marofe Hossain, Shantanu Baral, Ashab Uddin Al-Raiyan, Sabiba Bintay Ashraf, Weigui Sun

Abstract readSystematic Review
In one paragraph

Synthesis in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

11 citing papers in PubMed.

  1. Article
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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

6 authors.

Yeasin AhamedDepartment of Urology Surgery, The Affiliated Hospital of Yangzhou University, Yangzhou, 225001, Jiangsu, China.
Marofe HossainDepartment of Urology Surgery, The Affiliated Hospital of Yangzhou University, Yangzhou, 225001, Jiangsu, China.
Shantanu BaralDepartment of Urology Surgery, The Affiliated Hospital of Yangzhou University, Yangzhou, 225001, Jiangsu, China.
Ashab Uddin Al-RaiyanDepartment of Urology Surgery, The Affiliated Hospital of Yangzhou University, Yangzhou, 225001, Jiangsu, China.
Sabiba Bintay AshrafDhaka, Medical College for Women and Hospital, Dhaka University, Dhaka, 1230, People's Republic of Bangladesh.
Weigui SunDepartment of Urology Surgery, The Affiliated Hospital of Yangzhou University, Yangzhou, 225001, Jiangsu, China. xiaoyang168936@outlook.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis review offers a distinctive perspective by integrating and critically evaluating the latest advancements in non-invasive biomarkers for Prostate-Specific Antigen (PSA) gray-zone prostate cancer. By synthesizing data on Prostate Health Index (PHI), Prostate Cancer Antigen 3 (PCA3), Transmembrane Protease Serine 2-ETS-related Gene fusion (TMPRSS2-ERG fusion gene), proteomics, and microRNA (miRNAs), this work highlights their potential to enhance diagnostic precision while minimizing unnecessary biopsies. Furthermore, this review explores the clinical applicability of these biomarkers, bridging the gap between research innovations and real-world diagnostic strategies.The primary objective of this review is to analyze emerging biomarkers and clinical indicators that address the inherent diagnostic uncertainties within the PSA gray zone (4-10 ng/mL).Given the overlap between benign and malignant conditions in this range, traditional PSA-based screening lacks specificity, often leading to overdiagnosis and overtreatment.This review critically examines the diagnostic performance of the free PSA/total PSA (fPSA/tPSA) ratio, the Prostate Health Index (PHI), and molecular markers such as PCA3 and TMPRSS2-ERG fusion genes.Additionally, we discuss the integration of proteomic and miRNA-based approaches, emphasizing their potential role in refining risk stratification and advancing non-invasive prostate cancer diagnostics.

methodsA systematic review was conducted focusing on peer-reviewed research from databases such as PubMed, MEDLINE, and others.The studies included reported diagnostic accuracy, sensitivity, specificity, and clinical outcomes for biomarkers associated with PSA gray-zone prostate cancer.The inclusion criteria emphasized studies that evaluated human subjects and presented measurable diagnostic outcomes related to fPSA/tPSA ratio, PHI, PCA3, TMPRSS2-ERG, and additional protein-based biomarkers.

resultsThe findings reveal that the fPSA/tPSA ratio enhances diagnostic sensitivity and specificity, making it a valuable tool within the PSA gray zone.PHI demonstrates superior diagnostic accuracy compared to traditional markers like tPSA.Molecular markers, such as PCA3 and TMPRSS2-ERG fusion genes, show considerable potential for distinguishing between benign and malignant conditions, effectively reducing the need for unnecessary biopsies.Additionally, proteomics and glycoprotein biomarkers offer non-invasive diagnostic possibilities, although further validation is necessary to confirm their efficacy.

conclusionIncorporating multiple biomarkers, including the fPSA/tPSA ratio, PHI, PCA3, and TMPRSS2-ERG, presents a more accurate and patient-friendly approach to diagnosing PSA gray-zone prostate cancer.This multi-marker strategy enhances diagnostic precision, reduces biopsy rates, and supports the early detection of aggressive disease forms, representing a significant step forward in prostate cancer management and prognosis.

Indexed as

Biomarkers, TumorProstate-Specific AntigenProstatic NeoplasmsAntigens, NeoplasmEarly Detection of CancerHumansMaleMicroRNAsOncogene Proteins, FusionProteomicsAntigens, NeoplasmBiomarkers, TumorMicroRNAsOncogene Proteins, Fusionprostate cancer antigen 3, humanProstate-Specific AntigenTMPRSS2-ERG fusion protein, humanProstate health indexProteomicsPSA gray-zone prostate cancer

Identifiers

PMID40760471
PMCPMC12323064

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.