Oshima C, Nagai M, Marques L, Brentani M
UNIV SAO PAULO,FAC MED,DEPT RADIOL,DISCIPLINA ONCOL,BR-01246000 SAO PAULO,BRAZIL. FUNDACAO ONCOCENTRO SAO PAULO,SAO PAULO,BRAZIL. HOSP AC CARMARGO FUNDACAO ANTONIO PRUDENTE,SAO PAULO,BRAZIL.
Int J Oncol. 1995 Mar;6(3):719-23. doi: 10.3892/ijo.6.3.719.
The level of c-myc messenger RNA was measured in 105 primary breast carcinoma samples and matched normal breast tissue from the same patients. Only tumors showing a greater than 2-fold increase in c-myc levels were considered to be overexpressed. Overexpression of c-myc mRNA was identified in 27.6% of tumor samples analysed and was significantly correlated with mitotic grade (p=0.05) and intense lymphocytic infiltrate (p=0.026) but not with other clinical and pathological variables such as size, necrosis, lymph node involvement, estrogen or progesterone receptor status, menopausal status, age or staging of the patients and increased risk of relapse or overall survival. Approximately 25% of the tumors contained overexpression of c-erbB-2 mRNA and simultaneous overexpression of the two oncogenes was seen in only five samples. Disease-free survival was significantly shorter in these patients (p=0.02) and this reduction remained significant after adjustment for nodal status. However, simultaneous overexpression of c-myc and c-erbB-2 did not improve significantly the prediction of risk of death.
在105例原发性乳腺癌样本以及来自同一患者的配对正常乳腺组织中检测了c-myc信使核糖核酸(mRNA)的水平。只有那些c-myc水平升高超过2倍的肿瘤才被认为是过表达。在分析的肿瘤样本中,27.6%的样本存在c-myc mRNA过表达,且其与有丝分裂分级(p = 0.05)和密集淋巴细胞浸润(p = 0.026)显著相关,但与其他临床和病理变量无关,如肿瘤大小、坏死情况、淋巴结受累情况、雌激素或孕激素受体状态、绝经状态、患者年龄或分期,以及复发风险增加或总生存率。约25%的肿瘤存在c-erbB-2 mRNA过表达,仅在5个样本中观察到两种癌基因同时过表达。这些患者的无病生存期显著缩短(p = 0.02),在调整淋巴结状态后,这种缩短仍具有显著性。然而,c-myc和c-erbB-2同时过表达并不能显著改善死亡风险的预测。