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Updated: Oct 2, 2025

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Optimization of a Multiplex RNA-based Expression Assay Using Breast Cancer Archival Material
Published on: August 1, 2018
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Transcribed Ultraconserved Regions Are Associated with Clinicopathological Features in Breast Cancer
Erika Pereira Zambalde1, Douglas Adamoski2, Daniela Fiori Gradia1
1Laboratory of Human Cytogenetics and Oncogenetics, Department of Genetics, Universidade Federal do Paraná, Curitiba 81531-980, PR, Brazil.
Biomolecules
|February 25, 2022
Summary
Transcriptionally active ultraconserved regions (T-UCRs) show promise as breast cancer (BC) biomarkers. Specific T-UCRs correlate with patient age, tumor characteristics, and receptor status, aiding in BC subtype classification.
Area of Science:
- Genomics
- Molecular Biology
- Cancer Research
Background:
- Ultraconserved regions (UCRs) are highly conserved genomic segments.
- Transcriptionally active UCRs (T-UCRs) produce non-coding RNAs.
- Previous work linked T-UCR expression to breast cancer (BC) parameters.
Purpose of the Study:
- Investigate the expression of 12 T-UCRs in BC.
- Correlate T-UCR expression with clinicopathological factors and survival.
- Evaluate T-UCRs as potential BC biomarkers.
Main Methods:
- Analyzed expression of 12 T-UCRs in TCGA and Brazilian BC cohorts.
- Correlated T-UCR levels with clinicopathological parameters and immunohistochemical markers.
- Assessed T-UCR panel performance in distinguishing BC subtypes.
Main Results:
- uc.268 expression linked to younger age, ER/PR positivity, and Luminal A BC.
- Lower uc.84 and uc.376 associated with metastatic/stage IV Luminal B tumors.
- A panel of uc.147, uc.271, uc.427 differentiated Luminal A from triple-negative BC (AUC 0.9531).
Conclusions:
- T-UCRs demonstrate significant correlations with BC characteristics.
- Specific T-UCRs may serve as prognostic and diagnostic biomarkers for BC.
- T-UCR panels show potential for accurate BC subtype classification.
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