马戏团:软组织肉瘤中的循环肿瘤细胞-一个简短的报告。

IF 4.6 Q1 ONCOLOGY 癌症耐药(英文) Pub Date : 2024-12-13 eCollection Date: 2024-01-01 DOI:10.20517/cdr.2024.149
Robin J Young, Joanna E Chowdry, Denis Cochonneau, Dominique Heymann
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引用次数: 0

摘要

目的:循环肿瘤细胞(ctc)可以通过其物理特性(比正常循环血细胞大小增加且不易变形)或使用细胞表面标记物在外周血中检测。对这些CTCs的研究应该为肿瘤生物学提供重要的见解,包括耐药机制。我们进行了一项试点研究(IRAS ID: 235459),以评估是否可以从软组织肉瘤(STS)患者的外周血样本中分离出ctc。方法:我们采用了一种联合方法,首先使用微流控盒通过ParosrtixTMPR1富集ctc样品,然后使用DEPArrayTM对染色的vimentin和细胞角蛋白进行分选。同时分析循环游离细胞DNA (cfDNA)水平。数据与临床参数相关。结果:本研究招募了13例患者,其中7例为局部疾病,6例为转移性疾病。基于间充质和上皮标记物的表达,ctc表现出高度的异质性。在局部和转移性疾病患者中,ctc的数量没有显著差异。我们观察到CTC数与cfDNA没有相关性;然而,ctc的数量确实与原发肿瘤的大小相关。结论:本研究证实了局部和晚期STS患者存在CTCs。需要进一步和更大规模的研究来确定STS ctc的特征并评估其预后意义。
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CIRCUS: CIRCUlating tumour cells in soft tissue Sarcoma - a short report.

Aims: 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. Methods: We used a combined approach that first enriched samples for CTCs using a microfluidic cassette via ParosrtixTMPR1, and then sorted cells stained for vimentin and cytokeratin using the DEPArrayTM. The total circulating cell-free DNA (cfDNA) level was also analysed. Data were correlated with clinical parameters. Results: 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. Conclusion: 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.

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Mechanisms of immunotherapy resistance in small cell lung cancer. Mitochondrial genome variability and metabolic alterations reveal new biomarkers of resistance in testicular germ cell tumors. Ovarian tumor microenvironment contributes to tumor progression and chemoresistance. Role of the TME in immune checkpoint blockade resistance of non-small cell lung cancer. CIRCUS: CIRCUlating tumour cells in soft tissue Sarcoma - a short report.
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