<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-19T02:18:23Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10084" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10084</identifier><datestamp>2026-10-18T21:13:05Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Evaluation of S100A4, CA-12, CA-9, Annexin A1/A2, and Galectin-3 in Prostate Cancer: Diagnostic and Prognostic Implications</dc:title><dc:creator>Aslan, Rahmi</dc:creator><dc:creator>Huyut, Zübeyir</dc:creator><dc:creator>Keleş, Muhammed Fatih</dc:creator><dc:creator>Bedir, Nedim</dc:creator><dc:creator>Eryılmaz, Recep</dc:creator><dc:creator>Huyut, Mehmet Tahir</dc:creator><dc:creator>Saygın, Murat</dc:creator><dc:creator>Demir, Murat</dc:creator><dc:creator>Taken, Kerem</dc:creator><dc:subject>Annexin A1</dc:subject><dc:subject>Annexin A2</dc:subject><dc:subject>Biomarkers, Tumor</dc:subject><dc:subject>Carbonic Anhydrases</dc:subject><dc:subject>Prostatic Neoplasms</dc:subject><dc:subject>S100A4 Protein</dc:subject><dc:subject>Aged</dc:subject><dc:subject>Case-Control Studies</dc:subject><dc:subject>Follow-Up Studies</dc:subject><dc:subject>Galectin 3</dc:subject><dc:subject>Humans</dc:subject><dc:subject>Male</dc:subject><dc:subject>Middle Aged</dc:subject><dc:subject>Prognosis</dc:subject><dc:subject>Prospective Studies</dc:subject><dc:subject>ROC Curve</dc:subject><dc:subject>S100 Calcium-Binding Protein A4</dc:subject><dc:subject>ANXA1 protein, human</dc:subject><dc:subject>ANXA2 protein, human</dc:subject><dc:subject>calvasculin</dc:subject><dc:subject>lipocortin 1</dc:subject><dc:subject>lipocortin 2</dc:subject><dc:subject>S100A4 protein, human</dc:subject><dc:subject>tumor marker</dc:subject><dc:subject>blood</dc:subject><dc:subject>case control study</dc:subject><dc:subject>diagnosis</dc:subject><dc:subject>follow up</dc:subject><dc:subject>human</dc:subject><dc:subject>pathology</dc:subject><dc:description>Objective: The limited specificity of prostate-specific antigen (PSA) increases the risk of unnecessary biopsies and overtreatment. This study aimed to evaluate the diagnostic and prognostic value of serum S100A4, along with CA-9, CA-12, Annexin A1/A2, and Galectin-3, in prostate cancer. Methods: This prospective case-control study, conducted between July 2024 and September 2025, included 80 patients with histopathologically confirmed prostate cancer and 40 age-matched healthy controls. Patients were stratified into low-risk (ISUP grades 1-2) and high-risk (ISUP ≥ 3) groups. Serum biomarker levels were measured using ELISA. Diagnostic and prognostic performance was assessed by receiver operating characteristic (ROC) analysis, with cut-off values determined using the Youden index. Logistic regression analyses were performed to identify independent biomarkers. Results: Serum CA-12 and CA-9 levels were significantly higher in prostate cancer patients than in controls (p = 0.004 and p = 0.032, respectively). Although S100A4 levels were lower in prostate cancer patients compared with controls, they were significantly higher in high-risk patients within the cancer cohort (p = 0.002). Logistic regression identified S100A4 (p = 0.032) and CA-12 (p = 0.004) as independent predictors of prostate cancer diagnosis. ROC analysis demonstrated excellent diagnostic accuracy for CA-12 (&gt;52.9 ng/mL; AUC = 0.99) and S100A4 (&lt;9.96 ng/mL; AUC = 0.98). For prognostic stratification, S100A4 (&gt;8.27 ng/mL; AUC = 0.97) and CA-12 (&gt;72.8 ng/mL; AUC = 0.91) effectively distinguished high-risk from low-risk disease. Conclusion: S100A4 and CA-12 exhibit strong diagnostic and prognostic performance in prostate cancer. When used alongside PSA, S100A4 and CA-12 may improve risk stratification in patients with suspected prostate cancer and help reduce unnecessary prostate biopsies. This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License.</dc:description><dc:publisher>Asian Pacific Organization for Cancer Prevention</dc:publisher><dc:date>2026</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/10084</dc:identifier><dc:identifier>https://doi.org/10.31557/apjcp.2026.27.9.3281</dc:identifier><dc:identifier>1513-7368</dc:identifier><dc:language>en</dc:language><dc:relation>Asian Pacific Journal of Cancer Prevention</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/10084</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>