ArticleInternational journal of genomics2026
Single-Cell Transcriptomics Reveals the Potential Role of GZMK+ CD8+ T Cells in Cell Senescence of Triple-Negative Breast Cancer.
Article in International journal of genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- Single-Cell Transcriptomics Reveals the Potential Role of GZMK+ CD8+ T Cells in Cell Senescence of Triple-Negative Breast Cancer.International journal of genomics · 2026Article
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Senescence is a critical risk factor for the development of triple-negative breast cancer (TNBC), yet its specific impact on the disease remains inadequately understood. This study aims to elucidate the role of pivotal genes in mediating the effects of gene expression on cell senescence and TNBC progression. We employed a combination of Mendelian randomization (MR) and single-cell RNA sequencing to investigate these relationships. A two-sample MR approach was utilized to assess causal links between pivotal genes and TNBC. Single-cell transcriptomic analysis of senescence and TNBC datasets from the Gene Expression Omnibus database revealed a significant association between the gene GZMK and increased TNBC risk. Our single-cell analysis uncovered a complex network of ligand-receptor interactions in GZMK + central memory CD8+ T cells (CD8_CM), which frequently interacted with macrophages, monocytes, and epithelial cells. GZMK expression was correlated with pseudotime progression, indicating its potential role in TNBC development. Enrichment analysis suggested that GZMK + CD8_CM cells play a role in enhancing immune process regulation, pointing to a broader immune response. Bulk sequencing further confirmed the presence of GZMK expression in TNBC samples. Functional experiments demonstrated that GZMK significantly influences the proliferation, migration, and invasion of TNBC cell lines
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