MRPS28 serves as a biomarker of diagnostic, prognostic, and immune modulation in pan-cancer and promotes breast cancer malignant phenotypes.
[BACKGROUND] MRPS28 (Mitochondrial Ribosomal Protein S28) belongs to the MRP family and plays a critical role in mitochondrial translation and cellular energy metabolism.
APA
Guo X, Wang S, et al. (2026). MRPS28 serves as a biomarker of diagnostic, prognostic, and immune modulation in pan-cancer and promotes breast cancer malignant phenotypes.. Frontiers in immunology, 17, 1680772. https://doi.org/10.3389/fimmu.2026.1680772
MLA
Guo X, et al.. "MRPS28 serves as a biomarker of diagnostic, prognostic, and immune modulation in pan-cancer and promotes breast cancer malignant phenotypes.." Frontiers in immunology, vol. 17, 2026, pp. 1680772.
PMID
41853286
Abstract
[BACKGROUND] MRPS28 (Mitochondrial Ribosomal Protein S28) belongs to the MRP family and plays a critical role in mitochondrial translation and cellular energy metabolism. However, the effect of MRPS28 in pan-cancer remains unknown. This study aimed to perform a comprehensive assessment of the oncogenic potential of MRPS28 in pan-cancer using several databases, with a particular focus on breast cancer.
[METHODS] The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases were employed to evaluate MRPS28 expression across pan-cancer. Furthermore, we analyzed the association between the expression of MRPS28 and diagnosis, prognosis, genetic alterations, genomic heterogeneity, DNA methylation, and immunity. In addition, the biological function of MRPS28 in breast cancer was investigated. The role of MRPS28 in the malignant biological behavior of breast cancer cells was studied through experiments, including cell proliferation, migration, and invasion.
[RESULTS] Our analyses indicated that MRPS28 expression dysregulation was noted in various cancer types, and MRPS28 had remarkable diagnostic and prognostic predictive values. MRPS28 expression was substantially related to genetic alterations, genomic heterogeneity, and DNA methylation levels. In addition, MRPS28 was associated with immune infiltration and immune-related gene expression in multiple cancer types. Moreover, our experimental validation confirmed that MRPS28 knockdown considerably suppressed proliferation, migration, and invasion, as well as promoted apoptosis in the breast cancer cell lines MDA-MB-231 and MCF-7.
[CONCLUSION] Collectively, these findings imply that MRPS28 emerges as a potential diagnostic and prognostic biomarker across pan-cancer, with a potential oncogenic role in breast cancer progression. Furthermore, it may be a potential therapeutic target for various cancers.
[METHODS] The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases were employed to evaluate MRPS28 expression across pan-cancer. Furthermore, we analyzed the association between the expression of MRPS28 and diagnosis, prognosis, genetic alterations, genomic heterogeneity, DNA methylation, and immunity. In addition, the biological function of MRPS28 in breast cancer was investigated. The role of MRPS28 in the malignant biological behavior of breast cancer cells was studied through experiments, including cell proliferation, migration, and invasion.
[RESULTS] Our analyses indicated that MRPS28 expression dysregulation was noted in various cancer types, and MRPS28 had remarkable diagnostic and prognostic predictive values. MRPS28 expression was substantially related to genetic alterations, genomic heterogeneity, and DNA methylation levels. In addition, MRPS28 was associated with immune infiltration and immune-related gene expression in multiple cancer types. Moreover, our experimental validation confirmed that MRPS28 knockdown considerably suppressed proliferation, migration, and invasion, as well as promoted apoptosis in the breast cancer cell lines MDA-MB-231 and MCF-7.
[CONCLUSION] Collectively, these findings imply that MRPS28 emerges as a potential diagnostic and prognostic biomarker across pan-cancer, with a potential oncogenic role in breast cancer progression. Furthermore, it may be a potential therapeutic target for various cancers.
MeSH Terms
Humans; Breast Neoplasms; Female; Biomarkers, Tumor; Prognosis; Ribosomal Proteins; Gene Expression Regulation, Neoplastic; Mitochondrial Proteins; Cell Line, Tumor; DNA Methylation; Cell Proliferation; Phenotype; Cell Movement; Immunomodulation
같은 제1저자의 인용 많은 논문 (5)
- Ginsenoside Rg5 inhibits colorectal cancer, at least partially by blocking the lysosomal degradation of colorectal cancer cells.
- A novel risk stratification strategy for precision prevention of gastric cancer based on clinicopathological features and IGFBP7.
- Macrophage-Derived CuET Vesicles Synergistically Enhance Paclitaxel Efficacy by Inhibiting Tumor Growth and Boosting Immunity in Breast Cancer.
- Dysregulation of CircZNF79(5) Modulates YBX1 Stability and Selective Autophagy to Drive Hepatocellular Carcinoma Progression.
- Malignant cell-secreted chemokines drive colorectal cancer progression through endothelial cell activation.