Evidence map›Paper›PMID 41847519›Full record

ArticleBreast cancer (Dove Medical Press)2026

Development of a Prognostic Stratification Model and Identification of BDH1 as an Oncoprotein in Breast Cancer Based on Subcluster-Specific Markers of B-Cell Subsets.

Shujuan Kang, Zhongxin Li, Chao Lv, Fenghua Zhang

Abstract read
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Article in Breast cancer (Dove Medical Press), 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shujuan KangDepartment of Surgery, Hebei Medical University, Shijiazhuang, Hebei, 050017, People's Republic of China.
Zhongxin LiDepartment of General Surgery, Handan Central Hospital, Handan, Hebei, 056002, People's Republic of China.
Chao LvDepartment of Dermatology, Affiliated Hospital of Hebei Engineering University, Handan, Hebei, 056002, People's Republic of China.
Fenghua ZhangDepartment of Surgery, Hebei Medical University, Shijiazhuang, Hebei, 050017, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study aimed to analyze the breast cancer (BC) microenvironment using single-cell RNA sequencing (scRNA-seq) data, develop a prognostic stratification model, and identify potential therapeutic targets and drugs. Methods: scRNA-seq, bulk transcriptomic data, and clinical information were obtained from EMBL-EBI (single cell data from 17 tumor samples), TCGA (1039 tumor samples), and GEO databases [GSE20685 (324 tumor samples), GSE42568 (104 tumor samples), and GSE88770 (117 tumor samples)]. scRNA-seq data were used to analyze the tumor microenvironment landscape of BC and retrieve subcluster-specific markers (SSMs). Subtypes of BC patients were defined based on SSMs and bulk transcriptomic data, and a prognostic risk model was constructed using machine learning. The characteristic therapeutic targets of high-risk patients were further identified and potential drugs were evaluated by molecular docking and cellular thermal shift assay. In vitro and in vivo experiments were conducted to explore the functions of the core target, 3-hydroxybutyrate dehydrogenase 1 (BDH1) and tretinoin, which modulated the malignant biological behaviors of BC. Results: A total of 2004 SSMs were identified. Six prognostic cell sub-clusters were identified, and 16 prognostic genes were identified from the SSMs of these six cell sub-clusters. Least absolute shrinkage and selection operator (LASSO)-Cox algorithm further identified four core genes, and a risk model was constructed. The overall survival time of BC patients in the high-risk group was shorter than that of the low-risk group, and the risk score was a predictor of prognosis in BC patients in both training dataset and validation datasets ( Conclusion: The prognostic stratification model is promising for evaluating the clinical outcomes of BC patients, and BDH1 is an important drug target for high-risk patients, and tretinoin represses the malignancy of BC cells via targeting BDH1.

Indexed as

breast cancermachine learningsingle-cell RNA sequencingtherapeutic targetstumor microenvironment

Identifiers

PMID41847519
PMCPMC12989285

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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.