Evidence map›Paper›PMID 42322380›Full record

ArticleDiscover oncology2026

A novel model for assessing lymph node metastasis and the immune microenvironment in breast cancer by integrating digital pathology images and transcriptomics.

Yongliang Sha, Huijie Zhuang, Yiqiu Wang, Hao Guo, Hui Cheng

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Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Yongliang Sha *Department of General Surgery, Xuzhou Central Hospital, Southeast University, 199 Jiefang South Road, Xuzhou, 221000, China.
Huijie Zhuang *Department of General Surgery, Xuzhou Central Hospital, Southeast University, 199 Jiefang South Road, Xuzhou, 221000, China.
Yiqiu WangDepartment of General Surgery, Xuzhou Central Hospital, Southeast University, 199 Jiefang South Road, Xuzhou, 221000, China.
Hao Guo *Department of General Surgery, Xuzhou Central Hospital, Southeast University, 199 Jiefang South Road, Xuzhou, 221000, China. 18952170908@189.cn.
Hui Cheng *Department of Gynecology and Obstetrics, Xuzhou Central Hospital, Southeast University, 199 Jiefang South Road, Xuzhou, 221000, China. chenghui.1983@163.com.

Funding

The Jiangsu Health Commission's scientific research project 2024033
6 · The paper itself

Abstract

BACKGROUND/

aimsAccurate prediction of the lymph node status is essential for clinical decision-making in breast cancer. This work aimed to develop a multimodal deep learning model that integrates gene expression data with hematoxylin and eosin (H&E)-stained whole slide images (WSIs) to predict lymph node metastasis (LNM) and assess the tumor microenvironment in breast cancer.

methodsThe Cancer Genome Atlas (TCGA) database was used to gather the clinicopathological data, transcriptome information, and WSIs of patients with breast cancer. WSIs from Xuzhou Central Hospital were used as external validations. Four deep learning models were used to build the LNM pathological model. The pathogenic model and hub genes provided the foundation for constructing the nomogram. The potential mechanism was evaluated through the performance of functional enrichment. The calibration, discrimination, and clinical usefulness of the pathological model, multi-gene model, and nomogram were evaluated. Furthermore, the correlation between the nomogram and prognosis, clinicopathological features, and the quantity of immune cells was evaluated. Using immunohistochemistry and popliteal lymph node metastasis tests, the expression of beta-1,3-galactosyltransferase-4 (B3GALT4) in tumor tissues and its association with LNM and CD8

resultsThe findings of the present study demonstrated that in comparison to any single model, the nomogram's area under the curve (AUC) was better, at 0.99 [95% CI: 0.98-1.00]. The calibration curve demonstrated a high degree of agreement. The bulk of the threshold probabilities in this model were linked to favorable net benefits. Compared to the low-risk group, patients with high-risk breast cancer had more CD8

conclusionsThis model may provide a higher predictive value for LNM. B3GALT4 could serve as a risk biomarker of lymph node metastatic breast cancer.

Indexed as

Bioinformatics analysisBreast cancerDeep learningLymph node metastasisTumor immune microenvironmentWhole slide images

Identifiers

PMID42322380
PMCPMC13438534

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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.