PIK3CA mutation analysis in circulating tumor cells of patients with hormone receptor positive metastatic breast cancer

IF 2.3 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Elena Marino , Cristian Mauro , Elena Belloni , Marco Picozzi , Valentina Favalli , Maria Cristina Cassatella , Laura Zorzino , Luciano Giacò , Pier Giuseppe Pelicci , Massimo Barberis , Maria Teresa Sandri , Loris Bernard
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引用次数: 0

Abstract

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.

激素受体阳性转移性乳腺癌患者循环肿瘤细胞中的 PIK3CA 基因突变分析
在转移性乳腺癌(MBC)中,血液是循环肿瘤细胞(CTC)的来源。CTCs 可作为 "实时液体活检",因为它们比原发肿瘤更能代表转移性肿瘤遗传学。PIK3CA 是对治疗无反应的乳腺癌中最重要的致癌基因之一。本研究旨在检测 MBC 患者 CTC 中的 PIK3CA 突变和遗传性癌症变异。研究人员从 20 名 MBC 患者身上采集了至少 1/3 个连续时间点的 47 份血液样本。使用 CellSearch 系统对 CTC 进行量化,并使用 DEPArray 系统从 11/20 例 CTC ≥5/7.5 ml 的患者(14/47 例血液样本)中分离出 CTC。提取并扩增 DNA,对 PIK3CA 基因进行 Sanger 测序。测序结果显示,2/11 个病例(18%)存在致病性 PIK3CA 基因突变。随后,我们通过下一代测序技术评估了 26 个目标遗传基因面板,并在一名 PIK3CA 基因突变的患者中发现了 TP53 基因的致病性突变。未发现致病性种系变异。我们的数据支持这样的结论,即 CTCs 分析可用于识别患者体内的基因突变,从而确定那些更有可能发生转移的患者。
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来源期刊
Biochemistry and Biophysics Reports
Biochemistry and Biophysics Reports Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
4.60
自引率
0.00%
发文量
191
审稿时长
59 days
期刊介绍: Open access, online only, peer-reviewed international journal in the Life Sciences, established in 2014 Biochemistry and Biophysics Reports (BB Reports) publishes original research in all aspects of Biochemistry, Biophysics and related areas like Molecular and Cell Biology. BB Reports welcomes solid though more preliminary, descriptive and small scale results if they have the potential to stimulate and/or contribute to future research, leading to new insights or hypothesis. Primary criteria for acceptance is that the work is original, scientifically and technically sound and provides valuable knowledge to life sciences research. We strongly believe all results deserve to be published and documented for the advancement of science. BB Reports specifically appreciates receiving reports on: Negative results, Replication studies, Reanalysis of previous datasets.
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