Evidence map›Paper›PMID 41342168›Full record

ArticleJMIR bioinformatics and biotechnology2025

Framework for Race-Specific Prostate Cancer Detection Using Machine Learning Through Gene Expression Data: Feature Selection Optimization Approach.

David Agustriawan, Adithama Mulia, Marlinda Vasty Overbeek, Vincent Kurniawan, Jheno Syechlo, Moeljono Widjaja, Muhammad Imran Ahmad

Abstract read
In one paragraph

Article in JMIR bioinformatics and biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

David Agustriawan *Faculty of Engineering and Informatics, Universitas Multimedia Nusantara, Scientia Garden Jalan Boulevard Gading Serpong, Tangerang, 15810, Indonesia, 62 877-8153-5936.ORCID 0000-0003-1185-1145
Adithama Mulia *Faculty of Engineering and Informatics, Universitas Multimedia Nusantara, Scientia Garden Jalan Boulevard Gading Serpong, Tangerang, 15810, Indonesia, 62 877-8153-5936.ORCID 0009-0005-6885-0575
Marlinda Vasty OverbeekFaculty of Engineering and Informatics, Universitas Multimedia Nusantara, Scientia Garden Jalan Boulevard Gading Serpong, Tangerang, 15810, Indonesia, 62 877-8153-5936.ORCID 0000-0003-2590-843X
Vincent Kurniawan *Faculty of Engineering and Informatics, Universitas Multimedia Nusantara, Scientia Garden Jalan Boulevard Gading Serpong, Tangerang, 15810, Indonesia, 62 877-8153-5936.ORCID 0009-0004-1238-5232
Jheno Syechlo *Faculty of Engineering and Informatics, Universitas Multimedia Nusantara, Scientia Garden Jalan Boulevard Gading Serpong, Tangerang, 15810, Indonesia, 62 877-8153-5936.ORCID 0009-0001-5557-5085
Moeljono Widjaja *Faculty of Engineering and Informatics, Universitas Multimedia Nusantara, Scientia Garden Jalan Boulevard Gading Serpong, Tangerang, 15810, Indonesia, 62 877-8153-5936.ORCID 0000-0003-3002-7426
Muhammad Imran Ahmad *Faculty of Electronic Engineering and Technology, Universiti Malaysia Perlis, Perlis, Malaysia.ORCID 0000-0002-9157-5998

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Previous machine learning approaches for prostate cancer detection using gene expression data have shown remarkable classification accuracies. However, prior studies overlook the influence of racial diversity within the population and the importance of selecting outlier genes based on expression profiles. Objective: We aim to develop a classification method for diagnosing prostate cancer using gene expression in specific populations. Methods: This research uses differentially expressed gene analysis, receiver operating characteristic analysis, and MSigDB (Molecular Signature Database) verification as a feature selection framework to identify genes for constructing support vector machine models. Results: Among the models evaluated, the highest observed accuracy was achieved using 139 gene features without oversampling, resulting in 98% accuracy for White patients and 97% for African American patients, based on 388 training samples and 92 testing samples. Notably, another model achieved a similarly strong performance, with 97% accuracy for White patients and 95% for African American patients, using only 9 gene features. It was trained on 374 samples and tested on 138 samples. Conclusions: The findings identify a race-specific diagnosis method for prostate cancer detection using enhanced feature selection and machine learning. This approach emphasizes the potential for developing unbiased diagnostic tools in specific populations.

Indexed as

classificationfeature selectiongene expressionmachine learningprostate cancerrace specificsupport vector machine

Identifiers

PMID41342168
PMCPMC12314727

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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.