<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>McNally CJ</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Almost 50,000 men in the United Kingdom (UK) are diagnosed each year with prostate cancer (PCa). Secondary referrals for investigations rely on serum prostate-specific antigen (PSA) levels and digital rectal examination. However, both tests lack sensitivity and specificity, resulting in unnecessary referrals to secondary care for costly and invasive biopsies.&lt;h4>Materials and methods&lt;/h4>Serum samples and clinical information were collected from &lt;i>N&lt;/i> = 125 age-matched patients (&lt;i>n&lt;/i> = 61 non-PCa and &lt;i>n&lt;/i> = 64 PCa) and analyzed using Biochip Array Technology on high-sensitivity cytokine array I (IL-2, IL-4, IL-6, IL-8, IL-10, IL-1α, IL-1β, TNFα, MCP-1, INFγ, EGF, and VEGF), cerebral array II (CRP, D-dimer, neuron-specific enolase, and sTNFR1), and tumor PSA on</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>837127</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9161691</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Novel Combination of Serum Markers in a Multivariate Model to Help Triage Patients Into "Low-" and "High-Risk" Categories for Prostate Cancer.</pubmed_title><pmcid>PMC9161691</pmcid><pubmed_authors>Watt J</pubmed_authors><pubmed_authors>Lamont JV</pubmed_authors><pubmed_authors>Pandha H</pubmed_authors><pubmed_authors>Ruddock MW</pubmed_authors><pubmed_authors>Fitzgerald P</pubmed_authors><pubmed_authors>McNally CJ</pubmed_authors><pubmed_authors>Kurth MJ</pubmed_authors><pubmed_authors>McKenna DJ</pubmed_authors><pubmed_authors>Moore T</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Novel Combination of Serum Markers in a Multivariate Model to Help Triage Patients Into "Low-" and "High-Risk" Categories for Prostate Cancer.</name><description>&lt;h4>Background&lt;/h4>Almost 50,000 men in the United Kingdom (UK) are diagnosed each year with prostate cancer (PCa). Secondary referrals for investigations rely on serum prostate-specific antigen (PSA) levels and digital rectal examination. However, both tests lack sensitivity and specificity, resulting in unnecessary referrals to secondary care for costly and invasive biopsies.&lt;h4>Materials and methods&lt;/h4>Serum samples and clinical information were collected from &lt;i>N&lt;/i> = 125 age-matched patients (&lt;i>n&lt;/i> = 61 non-PCa and &lt;i>n&lt;/i> = 64 PCa) and analyzed using Biochip Array Technology on high-sensitivity cytokine array I (IL-2, IL-4, IL-6, IL-8, IL-10, IL-1α, IL-1β, TNFα, MCP-1, INFγ, EGF, and VEGF), cerebral array II (CRP, D-dimer, neuron-specific enolase, and sTNFR1), and tumor PSA on</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T13:18:25.931Z</modification><creation>2024-11-09T08:40:58.293Z</creation></dates><accession>S-EPMC9161691</accession><cross_references><pubmed>35664747</pubmed><doi>10.3389/fonc.2022.837127</doi></cross_references></HashMap>