Evidence map›Paper›PMID 41659840›Full record

ArticleHealth information science and systems2026

A data fusion deep learning approach for accurate organelle-based classification of cancer cells.

Harrison Yee, Megan Bouyea, Joshua Goldwag, John M Lamar, Xavier Intes, Uwe Kruger, Margarida Barroso

Abstract read
In one paragraph

Article in Health information science and systems, 2026. 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.

Harrison YeeDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY USA.ORCID 0009-0005-8580-1695
Megan BouyeaDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY USA.
Joshua GoldwagDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY USA.
John M LamarDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY USA.
Xavier IntesDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY USA.
Uwe KrugerDepartment of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY USA.
Margarida BarrosoDepartment of Molecular and Cellular Physiology, Albany Medical College, Albany, NY USA.

Funding

Endosome-mitochondria interactions in breast cancer cellsR01CA233188 · NCI · ALBANY MEDICAL COLLEGE · PI BARROSO, MARGARIDA · 2020 to 2024
$2.8M
IMAT-ITCR Collaboration: Artificial intelligence enhanced breast cancer dormancy cell classification-based organelle-morphology and topologyR21CA274622 · NCI · ALBANY MEDICAL COLLEGE · PI BARROSO, MARGARIDA, KRUGER, UWE · 2022 to 2023
$500k
NCI NIH HHS R01 CA233188NCI NIH HHS R21 CA274622
6 · The paper itself

Abstract

Purpose: Microscopy-based cancer cell classification traditionally relies on cell-based morphological features, while subcellular organelle organization remains underutilized. Existing machine learning methods often require manual preprocessing and handcrafted feature extraction, limiting scalability and introducing user bias. This study proposes an automated, interpretable, and organelle-focused deep learning framework for classifying breast cancer cell lines from high-resolution fluorescence microscopy images. Methods: We developed an end-to-end framework that incorporates patch-based sampling, sparsity filtering, and a channel-wise intermediate fusion strategy to independently extract and integrate organelle-specific features. Model interpretability was assessed using Grad-CAM visualizations and single-organelle classifier analyses. The framework was evaluated on fluorescence microscopy images from six breast cancer cell lines using 5-fold cross-validation. Results: The proposed framework achieved a classification accuracy of Conclusion: Organelle morphology and spatial organization provide strong discriminative signals for cancer cell classification. The proposed framework offers a scalable, automated, and interpretable deep learning solution that advances microscopy-based phenotyping and supports broader applications in computational pathology and cellular informatics. Graphical abstract:

Identifiers

PMID41659840
PMCPMC12881194

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.