Evidence map›Paper›PMID 41509399›Full record

ArticlebioRxiv : the preprint server for biology2026

MetaPaCS: A Novel Meta-Learning Framework for Pancreatic Cancer Subtype Identification.

Nick B Peterson, Mengtao Sun, Xinchao Wu, Jieqiong Wang, Shibiao Wan

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

5 authors.

Nick B PetersonDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE.ORCID 0009-0009-1189-7013
Mengtao SunDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE.ORCID 0009-0000-5071-2629
Xinchao WuDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE.ORCID 0009-0003-9265-9565
Jieqiong WangDepartment of Neurological Sciences, University of Nebraska Medical Center, Omaha, NE.
Shibiao WanDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE.ORCID 0000-0003-0661-2684

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Heather Colleen Jensen-Smith · 2012 to 2026
$59.2M
Using Patient-Reported Outcomes, Inflammatory Profiles, and Cardiovascular Phenogroups to Expand the Definition of Heart Failure with Preserved Ejection FractionP20GM152326 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Rebekah L. Gundry · 2024 to 2026
$10.3M
Leveraging Heterogenous Common Fund Data Sets and Beyond for Identifying Lung Cancer SubtypesR03OD038391 · OD · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI WAN, SHIBIAO, WANG, JIEQIONG · 2024 to 2024
$307k
NIGMS NIH HHS P20 GM103427NIGMS NIH HHS P20 GM152326NIH HHS R03 OD038391
6 · The paper itself

Abstract

As the third leading cause of cancer related deaths in the United States, pancreatic cancer (PaC) is a highly heterogenous malignancy that can be divided into a multitude of potential subtypes, with the main 4 consisting of aberrantly differentiated endocrine exocrine (ADEX), immunogenic, progenitor, and squamous. Each PaC subtype is characterized by unique molecular pathways and therapeutic characteristics. Identifying PaC molecular subtypes is essential for downstream patient risk stratification and tailored treatment design. Conventional wet-lab approaches for PaC subtyping like microdissection, histopathological studies or molecular profiling are often laborious, costly, and time-consuming. To address these concerns, we present MetaPaCS, a novel meta-learning framework to accurately identify PaC subtypes based on transcriptomics data only. Specifically, after preprocessing, the transcriptome-based feature vectors were classified by 10 base machine learning (ML) classifiers, whose prediction outputs were then combined with the initial preprocessed feature vectors to constitute a new set of ensemble feature vectors for a meta-learning model. Our meta-learning model could learn and leverage the diversity of different base classifiers to boost the prediction performance beyond any single ML model. Results based on 100 times ten-fold cross validation tests on benchmarking datasets demonstrated that MetaPaCS performed significantly better than existing state-of-the-art methods for PaC subtyping. In addition, our meta-learning model remarkably outperformed each individual base classifier, demonstrating that MetaPaCS could combine diverse results from multiple base classifiers to boost the ensemble performance. We believe that MetaPaCS is a promising tool for characterizing PaC subtypes and will have positive impacts on downstream risk stratification and personalized treatment design for PaC patients.

Indexed as

Cancer subtypingmeta learningPancreatic cancerStacking modelSubtype identification

Identifiers

PMID41509399
PMCPMC12776555

What OpenQuestion 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 OpenQuestion graph.