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Identification and Prognostic Analysis of Immune-Related Genes Co-Regulated by Key Histone Modifications in Breast
Yanni Cao1,2, Xiaohui Li1, Jiangshan Liu1
1School of Artificial Intelligence, Anhui University of Science & Technology, Huainan 232001, China.
Current Issues in Molecular Biology
|June 26, 2026
Summary
Histone modifications influence breast cancer (BRCA) development. This study identified key histone modifications and 11 immune-related genes that predict BRCA patient survival and treatment response.
Area of Science:
- Oncology
- Epigenetics
- Genomics
Background:
- Breast cancer (BRCA) is a prevalent malignancy significantly impacting women's health.
- Histone modifications (HMs) are implicated in the pathogenesis and progression of BRCA.
- Understanding HM patterns in normal (HMEC) and cancerous (MCF-7) cells is crucial for identifying therapeutic targets.
Purpose of the Study:
- To investigate the distribution of HMs in HMEC and MCF-7 cell lines.
- To analyze the association between HMs, gene expression, and BRCA patient outcomes.
- To develop a predictive model for BRCA prognosis and treatment efficacy.
Main Methods:
- Analysis of HM signal distribution in HMEC and MCF-7 cell lines.
- Application of algorithms to predict HM effects on gene expression.
- Screening of 268 HM-related immune-related genes (H_IRGs) and pathway analysis.
- Construction of a risk scoring model using Cox and LASSO regression.
Main Results:
- The random forest algorithm identified H3K4me2, H3K27me3, and H3K36me3 as key HMs influencing gene expression (AUC=0.92).
- A risk model was built using 11 key immune-related genes (IRGs).
- The model demonstrated effective prediction of patient survival in training and validation cohorts.
Conclusions:
- The study provides a theoretical framework for BRCA development.
- The identified 11 key IRGs show potential as biomarkers for BRCA prognostic assessment.
- These genes may also aid in predicting treatment response in breast cancer patients.
Related Concept Videos
Histone Modification
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...
Histone Modification
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...