Landscape of lncRNAs expressed in Mexican patients with triple‑negative breast cancer

  • 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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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.