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首页> 外文期刊>Japanese Journal of Cancer Research >Characterization of a new human embryonal rhabdomyosarcoma cell line, RMS-GR.
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Characterization of a new human embryonal rhabdomyosarcoma cell line, RMS-GR.

机译:新型人类胚胎横纹肌肉瘤细胞系RMS-GR的表征。

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A human tumor cell line designated RMS-GR was established from an embryonal rhabdomyosarcoma. The monolayer cells were polygonal, round or spindle-shaped. The RMS-GR cell line became stable with a doubling time of 42 h. Tumorigenicity of the cells was confirmed by heterotransplantion into nude mice. Electron microscopic images showed typical cytoplasmic inclusion of aggregated intermediate filaments and myofibril-like thin filaments. The expression of desmin, vimentin, actin and human myoglobin was recognized by cytofluorometric analyses, and a large fraction of CK-MM and small fractions of CK-BB and MCK-1 isoenzymes were found. Chromosomal analysis showed that the modal chromosome number was consistently near triploid with structural abnormalities mostly involving chromosomes 1, 3 and 8, and additional unidentified markers. No alteration of chromosome 2 was observed. The RMS-GR cell line may provide a system to identify genes which are involved in the pathogenic mechanism of rhabdomyosarcomas, and to investigate the modulation of myogenic differentiation.
机译:从胚胎横纹肌肉瘤建立了称为RMS-GR的人肿瘤细胞系。单层细胞为多边形,圆形或纺锤形。 RMS-GR细胞系变得稳定,倍增时间为42 h。通过异种移植到裸鼠中证实了细胞的致瘤性。电子显微镜图像显示聚集的中间丝和肌原纤维样细丝的典型细胞质内含物。通过细胞荧光分析识别了结蛋白,波形蛋白,肌动蛋白和人肌红蛋白的表达,并且发现了大部分的CK-MM,小部分的CK-BB和MCK-1同工酶。染色体分析表明,模态染色体数始终接近三倍体,具有结构异常,主要涉及1、3、8号染色体以及其他未识别标记。没有观察到2号染色体的改变。 RMS-GR细胞系可以提供一个系统,以鉴定与横纹肌肉瘤的发病机制有关的基因,并研究成肌分化的调控。

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