首页> 外文OA文献 >Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma.
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Homogeneously staining chromosomal regions contain amplified copies of an abundantly expressed cellular oncogene (c-myc) in malignant neuroendocrine cells from a human colon carcinoma.

机译:均质染色的染色体区域包含人类结肠癌恶性神经内分泌细胞中大量表达的细胞癌基因(c-myc)的扩增拷贝。

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摘要

Two human neuroendocrine tumor cell lines derived from a colon carcinoma contain either numerous double minute chromosomes (COLO 320 DM) or a homogeneously staining marker chromosome (COLO 320 HSR). We found amplification and enhanced expression of the cellular oncogene c-myc in both COLO 320 DM and HSR cells, and we were able to show that the homogeneously staining regions of the COLO 320 HSR marker chromosome contain amplified c-myc. From previous and present karyotypes, it appears that the homogeneously staining regions reside on a distorted X chromosome. Therefore, amplification of c-myc has been accompanied by translocation of the gene from its normal position on chromosome 8 (8q24). Because double minute chromosomes were features of primary cultures from the original tumor, it seems reasonable to suspect that amplification of c-myc may have contributed to tumorigenesis.
机译:源自结肠癌的两种人神经内分泌肿瘤细胞系包含许多双分钟染色体(COLO 320 DM)或同质染色标记染色体(COLO 320 HSR)。我们发现在COLO 320 DM和HSR细胞中细胞癌基因c-myc的扩增和表达增强,并且我们能够证明COLO 320 HSR标记染色体的均匀染色区域包含扩增的c-myc。从以前和现在的核型,似乎均匀染色区域位于扭曲的X染色体上。因此,c-myc的扩增伴随着基因从其在8号染色体(8q24)上的正常位置移位。由于每分钟染色体是原始肿瘤的原代培养特征,因此怀疑c-myc的扩增可能有助于肿瘤发生似乎是合理的。

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