Evidence map›Paper›PMID 41228248›Full record

ArticleCancers2025

TILDA-X: Transcriptome-Informed Lung Cancer Disparities via Explainable AI.

Masrur Sobhan, Md Mezbahul Islam, Mary Jo Trepka, Gregory E Holt, Charles J Dimitroff, Ananda M Mondal

Abstract read
In one paragraph

Article in Cancers, 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.

Masrur SobhanMachine Learning and Data Analytics Group (MLDAG), Knight Foundation School of Computing and Information Sciences, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-1515-4366
Md Mezbahul IslamMachine Learning and Data Analytics Group (MLDAG), Knight Foundation School of Computing and Information Sciences, Florida International University, Miami, FL 33199, USA.ORCID 0009-0008-4762-7843
Mary Jo TrepkaDepartment of Epidemiology, Robert Stempel College of Public Health & Social Work, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-6585-1194
Gregory E HoltDepartment of Medicine, University of Miami, Coral Gables, FL 33146, USA.
Charles J DimitroffDepartment of Cellular and Molecular Medicine, Herbert Wertheim College of Medicine, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-4224-7621
Ananda M MondalMachine Learning and Data Analytics Group (MLDAG), Knight Foundation School of Computing and Information Sciences, Florida International University, Miami, FL 33199, USA.ORCID 0000-0002-4005-9942

Funding

Analysis of galectin-8 and its ligands in melanoma progressionR01CA282520 · NCI · FLORIDA INTERNATIONAL UNIVERSITY · PI CHARLES J DIMITROFF · 2024 to 2026
$1.6M
FIU-Diversity Center for Genomic Research (FIU-DCGR)UG3HG013615 · NHGRI · FLORIDA INTERNATIONAL UNIVERSITY · PI BLACK, STEPHEN M, WANG, XUEXIA · 2024 to 2024
$817k
Explainable AI-Based Multi-Omics Analysis of Lung Cancer Health DisparityR21CA290324 · NCI · FLORIDA INTERNATIONAL UNIVERSITY · PI MONDAL, ANANDA MOHAN · 2024 to 2025
$371k
NCI NIH HHS R01 CA282520NCI NIH HHS R21 CA290324NHGRI NIH HHS UG3 HG013615NIH/NCI R21CA290324NIH/NHGRI UG3HG013615State of Florida Biomedical Research Program, Bankhead Coley Research Infrastructure 23B16
6 · The paper itself

Abstract

backgroundLung cancer is a leading cause of cancer-related mortality, with disparities in incidence and outcomes observed across different racial and sex groups. Identifying both patient-specific and cohort-specific disparity biomarkers is critical for developing targeted treatments. The lung cancer dataset is highly imbalanced across races, leading to biased results in disparity information if classification is based on race.

methodThis study developed an explainable artificial intelligence-based framework, TILDA-X, which designs classification models based on disease conditions instead of races to mitigate racial imbalance in the dataset and applies explainable AI to delineate patient-specific disparity information. A lung cancer transcriptome dataset with three disease conditions-lung adenocarcinoma, lung squamous cell carcinoma, and healthy samples-was used to develop classification models. Applying a bottom-up approach from patient-specific disparity information, the cohort-specific disparity information is discovered for different racial and sex groups, African American males, European American males, African American females, and European American females.

resultsClassification based on disease conditions achieved accuracy between 88% and 100% for minority groups (African American males and females), whereas it was only between 0% and 16% for race-based classification, which underscores the significance of the proposed approach. Functional analysis of sub-cohort-specific biomarker genes revealed unique pathways associated with lung cancers in different races and sexes. Among the significant pathways identified, over ~63% overlapped with previously reported lung cancer-related studies, supporting the biological validity of our findings. Overall, combining disease conditions-based classification with explainable AI, this study provides a robust, interpretable framework for characterizing race- and sex-specific disparities in lung cancer, offering a foundation for precision oncology and equitable therapeutic development based on transcriptome profile only.

Indexed as

explainable AIhealth disparitylung cancerpatient-specific biomarkerSHAP

Identifiers

PMID41228248
PMCPMC12607860

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.