首页> 美国卫生研究院文献>Cancer Science >Establishment of a Human Small Cell Lung Carcinoma Cell Line Carrying Amplification of c‐myc Gene and Chromosomal Translocation of t(3p;6p) and t(12q;17p)
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Establishment of a Human Small Cell Lung Carcinoma Cell Line Carrying Amplification of c‐myc Gene and Chromosomal Translocation of t(3p;6p) and t(12q;17p)

机译:建立携带c-myc基因扩增和t(3p; 6p)和t(12q; 17p)染色体易位的人小细胞肺癌细胞系

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摘要

A transplantable tumor and an in vitro culture cell line (GK‐T3) were established from metastatic liver tissue of human small cell lung carcinoma (SCLC). Southern blot analysis revealed about 30‐fold amplification of c‐myc gene in the tumor cells in liver, xenografts, and in vitro cell line. The degree of c‐myc amplification was essentially conserved through serial passages in nude mice and cultivation in vitro. The level of c‐myc mRNA was significantly increased in these cells. Cytogenetically, numerical and complex structural abnormalities were observed in GK‐T3 cells, including t(3p;6p), t(12q;17p), two homogeneously staining regions (hsrs) and several double minutes (dmins). These results suggest that activation of c‐myc gene and alteration of gene(s) round these chromosomal breakpoints may play a role in tumorigenesis of GK‐T3 SCLC.
机译:从人小细胞肺癌(SCLC)的转移性肝组织中建立了可移植的肿瘤和体外培养细胞系(GK-T3)。 Southern印迹分析表明,肝脏,异种移植物和体外细胞系中肿瘤细胞中c-myc基因的扩增约30倍。通过裸鼠中的连续传代和体外培养,c-myc扩增的程度基本上得以保留。这些细胞中c-myc mRNA的水平显着增加。在细胞遗传学上,在GK-T3细胞中观察到数值和复杂的结构异常,包括t(3p; 6p),t(12q; 17p),两个均匀染色区域(hsrs)和数分钟(dmins)。这些结果表明c-myc基因的激活和这些染色体断点周围基因的改变可能在GK-T3 SCLC的肿瘤发生中起作用。

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