Suppr超能文献

均匀染色的染色体区域包含来自人类结肠癌的恶性神经内分泌细胞中一个大量表达的细胞癌基因(c-myc)的扩增拷贝。

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

作者信息

Alitalo K, Schwab M, Lin C C, Varmus H E, Bishop J M

出版信息

Proc Natl Acad Sci U S A. 1983 Mar;80(6):1707-11. doi: 10.1073/pnas.80.6.1707.

Abstract

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.

摘要

源自结肠癌的两个人类神经内分泌肿瘤细胞系,一个含有大量双微体染色体(COLO 320 DM),另一个含有一条均匀染色的标记染色体(COLO 320 HSR)。我们发现细胞癌基因c-myc在COLO 320 DM和HSR细胞中均有扩增和表达增强,并且我们能够证明COLO 320 HSR标记染色体的均匀染色区域含有扩增的c-myc。从既往和目前的核型来看,均匀染色区域似乎位于一条畸变的X染色体上。因此,c-myc的扩增伴随着该基因从其在8号染色体(8q24)上的正常位置发生易位。由于双微体染色体是原始肿瘤原代培养物的特征,所以怀疑c-myc的扩增可能促成了肿瘤发生似乎是合理的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2474/393672/626cde1397b6/pnas00632-0229-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验