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Optimization of a Multiplex RNA-based Expression Assay Using Breast Cancer Archival Material
Published on: August 1, 2018
Histopathological evaluation of RPL5 expression in triple-negative breast cancer: an integrated immunohistochemical
Bing Zhao1, Peiyuan Yu1, Li Li1
1Department of Breast Cancer, Affiliated Tumor Hospital of Xinjiang Medical University, Urumqi.
European Journal of Histochemistry : EJH
|July 23, 2026
Summary
Triple-negative breast cancer (TNBC) shows altered ribosomal protein L5 (RPL5) expression. Lower RPL5 protein was found in TNBC tissues, but higher RPL5 gene expression was observed in TNBC compared to other breast cancers, suggesting a role in TNBC biology.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype with limited treatment options.
- Ribosomal protein L5 (RPL5) is involved in ribosome biogenesis and cellular processes.
- Understanding RPL5's role in TNBC is crucial for identifying new therapeutic targets.
Purpose of the Study:
- To investigate the expression pattern of RPL5 in TNBC tissues.
- To explore the potential biological significance of RPL5 in TNBC.
- To analyze the association of RPL5 with clinicopathological characteristics and survival outcomes.
Main Methods:
- Immunohistochemistry was used to evaluate RPL5 protein expression in 37 TNBC and 7 normal breast tissues.
- Public transcriptomic datasets (TCGA-BRCA, GEO) were analyzed for RPL5 gene expression.
- Co-expression, Gene Ontology, and KEGG pathway analyses were performed.
Main Results:
- RPL5 protein expression was significantly lower in TNBC tissues compared to normal tissues (p=0.001).
- RPL5 gene expression was significantly higher in TNBC compared to non-TNBC subtypes (p<0.001).
- No significant associations were found between RPL5 expression and clinicopathological parameters or overall survival.
Conclusions:
- Abnormal RPL5 expression is associated with TNBC biology, potentially via ribosome-related pathways.
- RPL5 may serve as a potential histopathological and molecular indicator for TNBC.
- Further experimental validation is required to elucidate the precise functional role of RPL5 in TNBC.