Evidence map›Paper›PMID 40004558›Full record

ArticleGenes2025

Unveiling Racial Disparities in Localized Prostate Cancer: A Systems-Level Exploration of the lncRNA Landscape.

Rebecca A Morgan, E Starr Hazard, Stephen J Savage, Chanita Hughes Halbert, Sebastiano Gattoni-Celli, Gary Hardiman

Abstract read
In one paragraph

Article in Genes, 2025. 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
–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

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

6 authors.

Rebecca A MorganFaculty of Medicine, Health and Life Sciences, School of Biological Sciences, Institute for Global Food Security (IGFS), Queen's University Belfast (QUB), Belfast BT9 5DL, UK.
E Starr HazardAcademic Affairs Faculty, Medical University of South Carolina (MUSC), Charleston, SC 29425, USA.
Stephen J SavageDepartment of Urology, Medical University of South Carolina (MUSC), Charleston, SC 29425, USA.
Chanita Hughes HalbertDepartment of Population and Public Health Sciences, University of Southern California, Los Angeles, CA 90033, USA.ORCID 0000-0002-0103-6916
Sebastiano Gattoni-CelliRalph H. Johnson VA Health Care System (VAHCS) Medical Center, Charleston, SC 29425, USA.
Gary HardimanFaculty of Medicine, Health and Life Sciences, School of Biological Sciences, Institute for Global Food Security (IGFS), Queen's University Belfast (QUB), Belfast BT9 5DL, UK.ORCID 0000-0003-4558-0400

Funding

Sociobiological Responses to Stress in Prostate Cancer SurvivorsU54MD010706 · NIMHD · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LENERT, LESLIE A. · 2016 to 2020
$8.0M
NIH HHS U54MD01070NIMHD NIH HHS U54 MD010706
6 · The paper itself

Abstract

BACKGROUND/

objectivesProstate cancer (PC) is the most common non-cutaneous cancer in men globally, and one which displays significant racial disparities. Men of African descent (AF) are more likely to develop PC and face higher mortality compared to men of European descent (EU). The biological mechanisms underlying these differences remain unclear. Long non-coding RNAs (lncRNAs), recognized as key regulators of gene expression and immune processes, have emerged as potential contributors to these disparities. This study aimed to investigate the regulatory role of lncRNAs in localized PC in AF men relative to those of EU and assess their involvement in immune response and inflammation.

methodsA systems biology approach was employed to analyze differentially expressed (DE) lncRNAs and their roles in prostate cancer (PC). Immune-related pathways were investigated through over-representation analysis of lncRNA-mRNA networks. The study also examined the effects of vitamin D supplementation on lncRNA expression in African descent (AF) PC patients, highlighting their potential regulatory roles in immune response and inflammation.

resultsKey lncRNAs specific to AF men were identified, with several being implicated for immune response and inflammatory processes. Notably, 10 out of the top 11 ranked lncRNAs demonstrated strong interactions with immune-related genes. Pathway analysis revealed their regulatory influence on antigen processing and presentation, chemokine signaling, and ribosome pathways, suggesting their critical roles in immune regulation.

conclusionsThese findings highlight the pivotal role of lncRNAs in PC racial disparities, particularly through immune modulation. The identified lncRNAs may serve as potential biomarkers or therapeutic targets to address racial disparities in PC outcomes.

Indexed as

Prostatic NeoplasmsRNA, Long NoncodingAgedBiomarkers, TumorBlack or African AmericanGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMaleMiddle AgedSystems BiologyWhiteBiomarkers, TumorRNA, Long Noncodingbiomarkersdifferential gene expressiongene regulatory networksimmune responseinflammationlong non-coding RNAs (lncRNAs)prostate cancerracial disparitiesvitamin D supplementation

Identifiers

PMID40004558
PMCPMC11855151

What Socratic holds

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LicenceCC BY
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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.