Young Robin J, Chowdry Joanna E, Cochonneau Denis, Heymann Dominique
Weston Park Cancer Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield S10 2SJ, UK.
School of Medicine and Population Health, University of Sheffield, Sheffield S10 2RX, UK.
Cancer Drug Resist. 2024 Dec 13;7:51. doi: 10.20517/cdr.2024.149. eCollection 2024.
Circulating tumour cells (CTCs) can be detected in peripheral blood using their physical properties (increased size and less deformable than normal circulating blood cells) or using cell surface markers. The study of these CTCs should provide important insights into tumour biology, including mechanisms of drug resistance. We performed a pilot study (IRAS ID: 235459) to evaluate if CTCs could be isolated from peripheral blood samples collected from soft tissue sarcoma (STS) patients. We used a combined approach that first enriched samples for CTCs using a microfluidic cassette via ParosrtixPR1, and then sorted cells stained for vimentin and cytokeratin using the DEPArray. The total circulating cell-free DNA (cfDNA) level was also analysed. Data were correlated with clinical parameters. 13 patients were recruited to this study: 7 patients with localised disease and 6 patients with metastatic disease. CTCs exhibited a high heterogeneity based on their expression of mesenchymal and epithelial markers. There was no significant difference in the number of CTCs between patients with localised versus metastatic disease. We observed no correlation between CTC numbers and cfDNA; however, the number of CTCs did correlate with primary tumour size. The present study demonstrates the presence of CTCs in STS patients with localised and advanced disease. Further and larger studies are needed to characterise STS CTCs and to evaluate their prognostic significance.
循环肿瘤细胞(CTCs)可通过其物理特性(体积增大且比正常循环血细胞更不易变形)或利用细胞表面标志物在外周血中被检测到。对这些CTCs的研究应能为肿瘤生物学提供重要见解,包括耐药机制。我们进行了一项试点研究(IRAS编号:235459),以评估能否从软组织肉瘤(STS)患者采集的外周血样本中分离出CTCs。我们采用了一种联合方法,首先通过ParosrtixPR1微流控盒富集CTCs样本,然后使用DEPArray对波形蛋白和细胞角蛋白染色的细胞进行分选。还分析了总循环游离DNA(cfDNA)水平。数据与临床参数相关。13名患者被纳入本研究:7名局部疾病患者和6名转移性疾病患者。基于间充质和上皮标志物的表达,CTCs表现出高度异质性。局部疾病患者和转移性疾病患者之间的CTCs数量无显著差异。我们观察到CTCs数量与cfDNA之间无相关性;然而,CTCs数量确实与原发肿瘤大小相关。本研究证明了局部和晚期疾病的STS患者中存在CTCs。需要进一步开展更大规模的研究来表征STS CTCs并评估其预后意义。