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PIK3CA mutation analysis in circulating tumor cells of patients with hormone receptor positive metastatic breast cancer
被引:0
|作者:
Marino, Elena
[1
,2
]
Mauro, Cristian
[3
]
Belloni, Elena
[4
]
Picozzi, Marco
[3
]
Favalli, Valentina
[5
]
Cassatella, Maria Cristina
[3
]
Zorzino, Laura
[3
]
Giaco, Luciano
[6
]
Pelicci, Pier Giuseppe
[4
,7
]
Barberis, Massimo
[1
]
Sandri, Maria Teresa
[8
]
Bernard, Loris
[1
]
机构:
[1] IRCCS, European Inst Oncol, Clin Unit Oncogen, IEO, Milan, Italy
[2] IRCCS, Ist Europeo Oncol, Lab Med Genet, Milan, Italy
[3] IRCCS, European Inst Oncol, Lab Med Div, IEO, Milan, Italy
[4] IRCCS, Ist Europeo Onc, Dept Expt Oncol, Milan, Italy
[5] 4Basessrl, Pavia, Italy
[6] Fdn Policlin Univ A Gemelli IRCCS, Bioinformat Core Facil, Gemelli Sci & Technol Pk G STeP, I-00168 Rome, Italy
[7] Univ Milan, Dept Oncol & Hematooncol, Milan, Italy
[8] Lab Bianal, Carate Brianza, MB, Italy
关键词:
Circulating tumor cells (CTCs);
Liquid biopsy;
Next generation sequencing (NGS);
JOINT-CONSENSUS-RECOMMENDATION;
SEQUENCE VARIANTS;
MUTATIONAL STATUS;
PIK3CA;
HETEROGENEITY;
ASSOCIATION;
GUIDELINES;
STANDARDS;
COLLEGE;
D O I:
10.1016/j.bbrep.2024.101805
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In metastatic breast cancer (MBC), blood is a source of circulating tumor cells (CTCs). CTCs may serve as a ''real-time liquid biopsy" as they represent metastatic tumor genetics better than primary tumor. PIK3CA is one of the most important oncogenes in treatment-unresponsive breast cancers. The aim of this study was to detect PIK3CA mutations and hereditary cancer variants in CTCs from MBC patients. Forty-seven blood samples were obtained from 20 MBC patients from at least 1/3 consecutive time points. CTCs were quantified using the CellSearch system and isolated from 11/20 patients with >= 5/7.5 ml CTCs (14/47 blood samples) using the DEPArray system. DNA was extracted and amplified to perform Sanger sequencing on PIK3CA gene. Sequencing revealed a pathogenic PIK3CA mutation in 2/11 (18 %) cases. Subsequently, we evaluated a 26-target hereditary gene panel by Next Generation Sequencing and identified a concomitant pathogenic mutation in the TP53 gene in a patient with a PIK3CA mutation. No pathogenic germline variants were found. Our data support the conclusion that CTCs analysis may be used to identify mutations in patients to identify those more likely to metastasize.
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