Aulmann Sebastian, Bentz Martin, Sinn Hans Peter
Department of Pathology, University of Heidelberg, Germany.
Breast Cancer Res Treat. 2002 Jul;74(1):25-31. doi: 10.1023/a:1016061327812.
The c-myc oncogene is frequently activated in invasive breast cancer and has been associated with high nuclear grade, lymph node metastasis and poorer disease outcome. We have examined c-myc oncogene amplification using fluorescence in situ hybridization in a series of 96 pure DCIS. Additionally we assessed amplification and expression of the Her2 and bcl-2 oncogenes. The findings were compared with clinicopathological data, Ki-67 proliferative index and hormone receptor status. We observed c-myc oncogene amplification in 19 tumours (20%). These cases were significantly associated with an average of 38% higher proliferative activity (p = 0.045), a 43% larger tumour size (p = 0.029) and the otherwise rare micropapillary subtype (p = 0.0005). Concluding the c-myc oncogene appears to be involved in the development of a more aggressive phenotype of DCIS.
c-myc癌基因在浸润性乳腺癌中常被激活,且与高核分级、淋巴结转移及较差的疾病预后相关。我们采用荧光原位杂交技术检测了96例纯导管原位癌(DCIS)中c-myc癌基因的扩增情况。此外,我们还评估了Her2和bcl-2癌基因的扩增及表达情况。将这些结果与临床病理数据、Ki-67增殖指数及激素受体状态进行了比较。我们在19例肿瘤(20%)中观察到了c-myc癌基因扩增。这些病例与平均高38%的增殖活性显著相关(p = 0.045),肿瘤大小平均大43%(p = 0.029),且与罕见的微乳头亚型相关(p = 0.0005)。结论是,c-myc癌基因似乎参与了DCIS更具侵袭性表型的发展。