Publicação
Public genomic cohort analyses reveal bcl6 expression as a prognostic marker in luminal a breast cancer
| datacite.subject.fos | Ciências Médicas | |
| datacite.subject.sdg | 03:Saúde de Qualidade | |
| dc.contributor.author | Barros, Patrícia | |
| dc.contributor.author | Gonçalves, Vânia | |
| dc.contributor.author | Jordan, Peter | |
| dc.contributor.author | Matos, Paulo | |
| dc.date.accessioned | 2026-03-04T12:19:03Z | |
| dc.date.available | 2026-03-04T12:19:03Z | |
| dc.date.issued | 2025-11-21 | |
| dc.description.abstract | Introduction: Breast cancer (BC) is the most common malignant neoplasm among women worldwide and remains a leading cause of cancer-related mortality. It is a heterogeneous disease classified into molecular subtypes with distinct prognostic and therapeutic implications. Luminal A is the most prevalent subtype, characterised by high expression of hormone receptors (oestrogen and progesterone), low proliferation rate, and generally favourable prognosis. However, consistent evidence indicates a significant risk of late recurrence and new neoplastic events, posing challenges for clinical follow-up strategies. Methodology: We analysed genomic data from the TCGA breast cancer cohort (n = 1247) to assess the prognostic value of the BCL6 gene, a transcriptional regulator previously implicated in tumour progression. Data on BCL6 expression, molecular subtyping (PAM50), and overall survival (OS) were retrieved. Results: Although BCL6 expression was globally reduced in tumours compared to normal tissue, it was significantly higher in Luminal A tumours than in other subtypes, with a subgroup (44%) maintaining expression levels similar to normal tissue. Importantly, within the Luminal A subtype, higher BCL6 expression was associated with poorer long term survival (p = 0.041). Discussion: These findings support the potential of BCL6 as a stratification biomarker for the risk of long term neoplasm recurrence within Luminal A breast cancer, with possible implications for tailoring the intensity and duration of clinical follow-up. | por |
| dc.identifier.uri | http://hdl.handle.net/10400.18/11103 | |
| dc.language.iso | eng | |
| dc.peerreviewed | yes | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | BCL-6 | |
| dc.subject | luminal A | |
| dc.subject | Prognostic Marker | |
| dc.subject | Breast Cancer | |
| dc.subject | Vias de Transdução de Sinal e Patologias Associadas | |
| dc.title | Public genomic cohort analyses reveal bcl6 expression as a prognostic marker in luminal a breast cancer | eng |
| dc.type | conference object | |
| dspace.entity.type | Publication | |
| oaire.citation.conferenceDate | 2026-11-20 | |
| oaire.citation.conferencePlace | Coimbra, Portugal | |
| oaire.citation.title | 29th Annual Meeting of the Portuguese Society of Human Genetics (SPGH), 20-22 novembro 2025 | |
| oaire.version | http://purl.org/coar/version/c_b1a7d7d4d402bcce |
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