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对一名患者在长期随访期间建立的三种小细胞肺癌细胞系的特征描述。

Characterization of three small cell lung cancer cell lines established from one patient during longitudinal follow-up.

作者信息

Berendsen H H, de Leij L, de Vries E G, Mesander G, Mulder N H, de Jong B, Buys C H, Postmus P E, Poppema S, Sluiter H J

机构信息

Department of Clinical Immunology, University Hospital, Groningen, The Netherlands.

出版信息

Cancer Res. 1988 Dec 1;48(23):6891-9.

PMID:2846164
Abstract

Three classic-type, small cell lung cancer cell lines (GLC-14, GLC-16, and GLC-19) have been established from one patient during longitudinal follow-up. During this period the tumor changed from sensitive to completely resistant to (chemo)therapy. A phenotypical and functional characterization of the different cell lines is given in combination with the matching clinical data. (a) The cell lines have been compared with the biopsies from which they were derived. There was a good match between the morphological, biochemical, and immunohistological findings in the cell lines as compared to those obtained in the biopsies. When the biopsy and cell line (GLC-14) obtained before the start of therapy were compared to the biopsies and cell lines (GLC-16 and GLC-19) acquired after the first and second reinduction therapy, respectively, no major changes could be observed. The only clear alteration was the loss of a neuroendocrine antigen (defined by monoclonal antibody MOC-51) in the posttherapy specimens. (b) The doxorubicin, melphalan, and etoposide sensitivity in vitro reflected the clinically observed development of resistance to treatment. The cell line (GLC-14) established before the start of therapy was more sensitive than the lines (GLC-16 and GLC-19) obtained after treatment. It is concluded that the cell lines described in this paper represent a well-characterized in vitro model in which the development of drug resistance in small cell lung cancer can be studied.

摘要

在长期随访期间,从一名患者身上建立了三种经典类型的小细胞肺癌细胞系(GLC - 14、GLC - 16和GLC - 19)。在此期间,肿瘤从对(化疗)敏感转变为完全耐药。结合匹配的临床数据,对不同细胞系进行了表型和功能特征分析。(a) 将这些细胞系与其来源的活检组织进行了比较。与活检组织相比,细胞系在形态学、生化和免疫组织学方面的发现具有良好的匹配性。当将治疗开始前获得的活检组织和细胞系(GLC - 14)与首次和第二次再诱导治疗后分别获得的活检组织和细胞系(GLC - 16和GLC - 19)进行比较时,未观察到重大变化。唯一明显的改变是治疗后标本中一种神经内分泌抗原(由单克隆抗体MOC - 51定义)的缺失。(b) 阿霉素、美法仑和依托泊苷的体外敏感性反映了临床上观察到的对治疗耐药性的发展。治疗开始前建立的细胞系(GLC - 14)比治疗后获得的细胞系(GLC - 16和GLC - 19)更敏感。结论是,本文所述的细胞系代表了一个特征明确的体外模型,可用于研究小细胞肺癌耐药性的发展。

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