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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by standudu
Group name EquipeCTCS
Item Type Journal Article
Title Quantification of HER1, HER2 and HER3 by time-resolved Förster resonance energy transfer in FFPE triple-negative breast cancer samples
Creator Ho-Pun-Cheung et al.
Author Alexandre Ho-Pun-Cheung
Author Hervé Bazin
Author Florence Boissière-Michot
Author Caroline Mollevi
Author Emeline Landas
Author Jean-Pierre Bleuse
Author Thierry Chardès
Author Jean-François Prost
Author André Pèlegrin
Author William Jacot
Author Gérard Mathis
Author Evelyne Lopez-Crapez
Abstract BACKGROUND: Triple-negative breast cancer (TNBC) has a worse prognosis compared with other breast cancer subtypes, and biomarkers to identify patients at high risk of recurrence are needed. Here, we investigated the expression of human epidermal receptor (HER) family members in TNBC and evaluated their potential as biomarkers of recurrence. METHODS: We developed Time Resolved-Förster Resonance Energy Transfer (TR-FRET) assays to quantify HER1, HER2 and HER3 in formalin-fixed paraffin-embedded (FFPE) tumour tissues. After assessing the performance and precision of our assays, we quantified HER protein expression in 51 TNBC specimens, and investigated the association of their expression with relapse-free survival. RESULTS: The assays were quantitative, accurate, and robust. In TNBC specimens, HER1 levels ranged from ?4000 to more than 2 million receptors per cell, whereas HER2 levels varied from ?1000 to 60,000 receptors per cell. HER3 expression was very low (less than 5500 receptors per cell in all samples). Moderate HER2 expression was significantly associated with higher risk of recurrence (HR?=?3.93; P?=?0.003). CONCLUSIONS: Our TR-FRET assays accurately quantify HER1, HER2 and HER3 in FFPE breast tumour specimens. Moderate HER2 expression may represent a novel prognostic marker in patients with TNBC.
Publication British Journal of Cancer
Date Dec 03, 2019
Journal Abbr Br. J. Cancer
Language eng
DOI 10.1038/s41416-019-0670-8
ISSN 1532-1827
Library Catalog PubMed
Extra 00000 PMID: 31792349
Tags original
Date Added 2020/01/21 - 10:47:00
Date Modified 2020/01/21 - 11:27:28
Notes and Attachments PubMed entry (Attachment)


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