Analysis of Circulating Tumor Cells, Lab of Analytical Chemistry, Department of Chemistry, University of Athens, Athens, Greece.
Medical School, University of Crete, Heraklion, Greece.
Clin Cancer Res. 2018 Mar 15;24(6):1500-1510. doi: 10.1158/1078-0432.CCR-17-1181. Epub 2017 Dec 28.
Liquid biopsy provides real-time monitoring of tumor evolution and response to therapy through analysis of circulating tumor cells (CTCs) and plasma-circulating tumor DNA (ctDNA). epigenetic silencing potentially affects response to endocrine treatment. We evaluated methylation in CTCs and paired plasma ctDNA. We evaluated methylation in CTCs and paired plasma ctDNA as a potential biomarker for response to everolimus/exemestane treatment. A highly sensitive and specific real-time MSP assay for methylation was developed and validated in (i) 65 primary breast tumors formalin-fixed paraffin-embedded (FFPE), (ii) EpCAM CTC fractions (122 patients and 30 healthy donors; HD), (iii) plasma ctDNA (108 patients and 30HD), and (iv) in CTCs (CellSearch) and in paired plasma ctDNA for 58 patients with breast cancer. methylation status was investigated in CTCs isolated from serial peripheral blood samples of 19 patients with ER/HER2 advanced breast cancer receiving everolimus/exemestane. methylation was detected in: (i) 25/65 (38.5%) FFPEs, (ii) : 26/112 (23.3%) patients and 1/30 (3.3%) HD, and (iii) 8/108 (7.4%) patients and 1/30 (3.3%) HD. methylation was highly concordant in 58 paired DNA samples, isolated from CTCs (CellSearch) and corresponding plasma. In serial peripheral blood samples of patients treated with everolimus/exemestane, methylation was observed in 10/36 (27.8%) CTC-positive samples, and was associated with lack of response to treatment ( = 0.023, Fisher exact test). We report for the first time the detection of methylation in CTCs and a high concordance with paired plasma ctDNA. methylation in CTCs was associated with lack of response to everolimus/exemestane regimen. methylation should be further evaluated as a potential liquid biopsy-based biomarker. .
液体活检通过分析循环肿瘤细胞 (CTC) 和血浆循环肿瘤 DNA (ctDNA) 提供肿瘤进化和对治疗反应的实时监测。表观遗传沉默可能会影响内分泌治疗的反应。我们评估了 CTC 中的甲基化和配对血浆 ctDNA。我们评估了 CTC 中甲基化作为对依维莫司/依西美坦治疗反应的潜在生物标志物。开发并验证了一种用于甲基化的高灵敏度和特异性实时 MSP 检测方法,该方法在 (i) 65 例福尔马林固定石蜡包埋 (FFPE) 原发性乳腺癌中,(ii) EpCAM CTC 分数 (122 例患者和 30 例健康供体;HD),(iii) 血浆 ctDNA (108 例患者和 30 例 HD),以及 (iv) 在细胞搜索中 CTC 和 58 例乳腺癌患者的配对血浆 ctDNA 中进行了验证。从 19 例接受依维莫司/依西美坦治疗的 ER/HER2 晚期乳腺癌患者的连续外周血样本中分离 CTC 后,对 CTC 中的甲基化状态进行了研究。在 (i) 25/65 (38.5%) FFPE 中,(ii) : 26/112 (23.3%) 患者和 1/30 (3.3%) HD 中,以及 (iii) 8/108 (7.4%) 患者和 1/30 (3.3%) HD 中检测到甲基化。在 58 对从 CTC (CellSearch) 和相应血浆中分离的 DNA 样本中,甲基化高度一致。在接受依维莫司/依西美坦治疗的患者的连续外周血样本中,在 10/36 (27.8%) CTC 阳性样本中观察到甲基化,并且与对治疗无反应相关 (= 0.023,Fisher 确切检验)。我们首次报道了 CTC 中甲基化的检测及其与配对血浆 ctDNA 的高度一致性。CTCs 中的甲基化与依维莫司/依西美坦方案无反应相关。甲基化应作为一种潜在的液体活检生物标志物进一步评估。