通过细针穿刺活检建立的黑色素瘤细胞系的发展和特征:转移性黑色素瘤患者监测的进展。

A I Riker, M C Panelli, U S Kammula, E Wang, J Wunderlich, A Abati, P Fetsch, S A Rosenberg, F M Marincola
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引用次数: 31

摘要

通过细针穿刺活检(FNAB)建立黑色素瘤细胞系,可以增强对T细胞和肿瘤细胞之间发生的复杂相互作用的理解。FNAB技术的优点是在整个治疗过程中对同一肿瘤结节进行序列分析。使用几种不同的方法评估新鲜黑色素瘤FNAB样本和来源于这些样本的肿瘤细胞系中黑色素瘤抗原(MAs)的表达。采用免疫细胞化学(ICC)分析新分离的肿瘤细胞外植体的细胞自旋制备,采用荧光活化细胞分选(FACS)、半定量和定量逆转录-聚合酶链反应(RT-PCR, qRT-PCR)分析子细胞系。通过这些方法评估,原始肿瘤细胞外植体的MA表达水平与体外建立的细胞系的表达水平相关。利用PCR技术对建立的细胞系进行分子分析,提高了检测MA表达的灵敏度。因此,黑色素瘤的FNAB是一种高效、有效的组织获取方法,能够从同一病灶连续产生新鲜肿瘤细胞、肿瘤浸润淋巴细胞(TIL)和长期黑色素瘤细胞系。
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Development and characterization of melanoma cell lines established by fine-needle aspiration biopsy: advances in the monitoring of patients with metastatic melanoma.

The establishment of melanoma cell lines from fine-needle aspiration biopsies (FNAB) has allowed for an enhanced understanding of the complex interactions that occur between T cells and tumor cells. The technique of FNAB offers the advantage of providing a sequential analysis of the same tumor nodules throughout treatment. The expression of melanoma antigens (MAs) was assessed in fresh melanoma FNAB samples and from tumor cell lines derived from these samples using several different approaches. Cytospin preparations of freshly isolated tumor cell explants were analyzed by immunocytochemistry (ICC), while the daughter cell line was analyzed by fluorescent activated cell sorting (FACS) analysis, and semiquantitative and quantitative reverse transcriptase-polymerase chain reaction (RT-PCR, qRT-PCR). As assessed by these methods, the level of MA expression by the original tumor cell explants correlated with the expression in established in vitro cell lines. Molecular analysis of the established cell lines utilizing PCR technology improved the sensitivity of detection of MA expression. Thus FNAB of melanoma is an efficient and effective method of tissue procurement, capable of generating, sequentially and from the same lesion, fresh tumor cells, tumor infiltrating lymphocytes (TIL), and long-term melanoma cell lines.

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