Landscape of lncRNAs expressed in Mexican patients with triple‑negative breast cancer
- 1Molecular Oncology Laboratory, Oncology Research Unit, XXI Century National Medical Center, The Mexican Institute of Social Security, Mexico City 06720, Mexico.
- 2Laboratory of Innovation in Precision Medicine, National Institute of Genomic Medicine, Mexico City 14610, Mexico.
- 3Department of Pathology, High Specialty Medical Unit Oncology Hospital, XXI Century National Medical Center, The Mexican Institute of Social Security, Mexico City 06720, Mexico.
- 4Molecular Biology Laboratory, Oncology Research Unit, XXI Century National Medical Center, The Mexican Institute of Social Security, Mexico City 06720, Mexico.
- 5Infectious and Parasitic Diseases Research Unit, XXI Century National Medical Center, The Mexican Institute of Social Security, Mexico City 06720, Mexico.
- 6Oncology Research Unit, XXI Century National Medical Center, The Mexican Institute of Social Security, Mexico City 06720, Mexico.
- 0Molecular Oncology Laboratory, Oncology Research Unit, XXI Century National Medical Center, The Mexican Institute of Social Security, Mexico City 06720, Mexico.
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View abstract on PubMed
Summary
This summary is machine-generated.Long non-coding RNAs (lncRNAs) show altered expression in triple-negative breast cancer (TNBC). Specific lncRNAs are linked to patient survival, offering potential biomarkers for improved TNBC clinical management.
Area Of Science
- Genomics
- Molecular Biology
- Oncology
Background
- Long non-coding RNAs (lncRNAs) are crucial gene expression regulators involved in cancer.
- Their stability and tissue specificity make them promising prognostic biomarkers.
- Triple-negative breast cancer (TNBC) requires novel biomarkers for improved patient stratification and management.
Purpose Of The Study
- To identify differentially expressed lncRNAs in Mexican patients with TNBC.
- To evaluate the potential of these lncRNAs as prognostic biomarkers for TNBC.
- To understand the role of lncRNAs in breast cancer progression and survival outcomes.
Main Methods
- Transcriptome analysis using Human Transcriptome Array 2.0 microarrays.
- Validation of differentially expressed lncRNAs in The Cancer Genome Atlas (TCGA) cohort, an independent Mexican cohort, and breast cancer cell lines.
- Correlation analysis between lncRNA expression levels and patient overall survival (OS).
Main Results
- 102 differentially expressed lncRNAs were identified in TNBC compared to luminal tumors.
- SOX9-AS was highly expressed in TNBC; Lnc-PXDN-3:1, Lnc-SYDE, and LINC01087 were decreased.
- Low expression of LINC01087, LINC02568, ACO22196, and Lnc-EGOT correlated with poor OS in TNBC patients.
- Specific lncRNAs (Lnc-PXDN-3:1, LINC00182, Lnc-GATA-3-1, LINC01087, BX679671.1, LINC00504, Lnc-ARHGEF38-IT1) were associated with survival in luminal and basal subtypes.
- LINC01087 was found to interact with RNAs and transcription factors, potentially involving the estrogen receptor pathway.
Conclusions
- This study identifies key lncRNAs with differential expression in Mexican TNBC patients.
- Several lncRNAs demonstrate prognostic value, correlating with overall survival in different breast cancer subtypes.
- These findings highlight lncRNAs as potential biomarkers for improved clinical management and understanding of TNBC.
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