Evidence map›Paper›PMID 41086385›Full record

ReviewJCO clinical cancer informatics2025

Large Language Models for Translational Cancer Informatics.

Yining Pan, Yanfei Wang, Guangyu Wang, Jing Su, Umit Topaloglu, Qianqian Song

Abstract readReview
In one paragraph

Review in JCO clinical cancer informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Yining PanDepartment of Health Outcomes and Biomedical Informatics, College of Medicine, University of Florida, Gainesville, FL.
Yanfei WangDepartment of Health Outcomes and Biomedical Informatics, College of Medicine, University of Florida, Gainesville, FL.
Guangyu WangCenter for Bioinformatics and Computational Biology, Houston Methodist Research Institute, Houston, TX.ORCID 0000-0003-4803-7200
Jing SuDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN.ORCID 0000-0003-4917-6173
Umit TopalogluCenter for Biomedical Informatics and Information Technology, National Cancer Institute, Rockville MDORCID 0000-0002-3241-8773
Qianqian SongDepartment of Health Outcomes and Biomedical Informatics, College of Medicine, University of Florida, Gainesville, FL.ORCID 0000-0002-4455-5302

Funding

Multi-modal insights of spatially distributed cells with associations of diseases and drug responseR35GM151089 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Qianqian Song · 2023 to 2026
$1.2M
NIGMS NIH HHS R35 GM151089
6 · The paper itself

Abstract

purposeCancer remains a leading cause of death worldwide. The growing volume of high-throughput single-cell and spatial transcriptomic data sets-particularly those related to cancer-offers immense opportunities as well as analytical challenges for effective data analysis and interpretation. Large language models (LLMs), pretrained on vast data sets and capable of various biomedical tasks, offer a promising solution. This review explores the application of LLMs in cancer research from both cellular and pathologic perspectives, aiming to showcase their potential in advancing precision oncology. MATERIALS AND

methodsWe systematically review current LLMs in analyzing single-cell RNA sequencing, spatial transcriptomic, and histology image data, emphasizing their relevance to cancer biology and translational research.

resultsA total of 24 LLMs, published or in preprint between 2022 and 2025, were selected for review. In single-cell transcriptomics, LLMs have primarily been used for cell type annotation, batch integration, and drug-response prediction. In spatial transcriptomics, LLMs support multislide and multimodal spatial data integration, gene expression imputation, niche and region label prediction, spatial domain identification, cell-cell communication inference, and marker gene detection. In computational pathology, LLMs have been applied to cancer subtyping, detection of rare malignancies, genomic mutation prediction, image segmentation, as well as cross-modal retrieval. Despite these advances, many models remain underoptimized for cancer-specific applications, highlighting the need for domain-specific fine-tuning and scalable adaptation strategies.

conclusionLLMs have the potential to significantly advance cancer research by providing scalable and effective tools for analyzing and interpreting single-cell, spatial transcriptomic, and pathology data. Future efforts should prioritize tailoring these models to cancer-specific contexts to enhance their utility in uncovering disease mechanisms, identifying biomarkers, and informing therapeutic strategies.

Indexed as

Computational BiologyNeoplasmsTranslational Research, BiomedicalHumansLarge Language ModelsSingle-Cell AnalysisTranscriptome

Identifiers

PMID41086385
PMCPMC13231491

What OpenQuestion holds

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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.