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Chronological occurrence of PI3KCA mutations in breast cancer liver metastases after repeat partial liver resection

Authors :
Aldrick Ruiz
Mylène Sebagh
Raphaël Saffroy
Marc-Antoine Allard
Nelly Bosselut
Giulia Hardoin
Julie Vasseur
Jocelyne Hamelin
René Adam
Jean-François Morère
Antoinette Lemoine
Source :
BMC Cancer, Vol 19, Iss 1, Pp 1-7 (2019)
Publication Year :
2019
Publisher :
BMC, 2019.

Abstract

Abstract Background Liver metastases of breast cancer are frequent and can recur even after “complete/R0” resection in combination with systemic and hormonal treatments. The aim of this study was to analyze throughout repeat hepatectomies for liver metastases the evolution of PI3KCA gene mutational status. Methods All liver metastases nodules (n = 70) from 19 women who underwent at least 2 liver resections were reexamined. DNA extraction from archived tumoral tissue was performed and the major ‘hot spot’ mutations in the helical and catalytic domains of PI3KCA have been analyzed using Massarray platform (Agena Bioscience) based on allelic discrimination PCR amplification followed by sensitive mass spectrometry detection. Results The two major somatic hot spot PI3KCA mutations were found in 27 (38.6%) nodules corresponding to 8 of the 19 patients (42%). The frequency of women whose breast cancer liver metastases (BCLM) carries PI3KCA mutations increased from the first to the third hepatectomy. Tumors carrying PI3KCA mutations are significantly larger and more frequently observed when resections were R0 compared to patients with no PI3KCA mutation. Conclusion PI3KCA mutations are frequently observed in BCLM and persist along with the recurrence. Their identification in circulating tumor cells should become a useful biomarker in the routine practice of breast cancer management to prevent tumor recurrence and overcome the problems of intra- and inter-tumoral heterogeneity of the current biomarkers,

Details

Language :
English
ISSN :
14712407
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
edsdoj.f1ca9cd2b7834ed2a8d2e85a895bf6e2
Document Type :
article
Full Text :
https://doi.org/10.1186/s12885-019-5365-2