van de Vijver M, van de Bersselaar R, Devilee P, Cornelisse C, Peterse J, Nusse R
Mol Cell Biol. 1987 May;7(5):2019-23. doi: 10.1128/mcb.7.5.2019-2023.1987.
We investigated alterations in the structure and expression of oncogenes in mammary tumors and mammary tumor-derived cell lines. In 16 of 95 samples, we detected amplification of the human neu oncogene, also known as c-erB-2, accompanied by overexpression in the tumors from which intact RNA could be isolated. In 10 of these DNAs, the linked oncogene c-erbA was also amplified, whereas another gene on human chromosome 17, p53, was present in normal copy numbers. Overexpression of c-erbA could not be detected in the tumors analyzed. The relatively high frequency of neu amplification points to a functional role in human breast cancer. Coamplification of the c-erbA oncogene could contribute to this disease as well but is most likely fortuitous.
我们研究了乳腺肿瘤及乳腺肿瘤衍生细胞系中癌基因结构和表达的改变。在95个样本中的16个样本里,我们检测到人类neu癌基因(也称为c-erB-2)的扩增,在能够分离出完整RNA的肿瘤中还伴有该基因的过表达。在这些DNA样本中的10个样本里,与之相关的癌基因c-erbA也发生了扩增,而人类17号染色体上的另一个基因p53的拷贝数则正常。在所分析的肿瘤中未检测到c-erbA的过表达。neu基因扩增的相对高频率表明其在人类乳腺癌中发挥功能性作用。c-erbA癌基因的共扩增也可能促成这种疾病,但很可能是偶然现象。