Ottestad L, Andersen T I, Nesland J M, Skrede M, Tveit K M, Nustad K, Børresen A L
Department of Medical Oncology, Norwegian Radium Hospital, Oslo.
Acta Oncol. 1993;32(3):289-94. doi: 10.3109/02841869309093597.
Primary tumours from 100 Norwegian node-negative breast carcinoma patients were examined for c-erbB-2, int-2, and c-myc proto-oncogene amplification. c-erbB-2, int-2, and c-myc amplification was found in 12.1% (12 of 99), 8.6% (8 of 93), and 1.1% (1 of 89) of the samples respectively. All the c-erbB-2 amplified tumours were of the ductal type, and all the int-2 amplified tumours were oestrogen receptor positive. No other significant or borderline significant associations between gene amplification and clinical or histopathological parameters were found. Relapse occurred more frequently in patients with c-erbB-2 gene amplification (relapse in 33.3% of the patients with c-erbB-2 amplification compared to 20.7% in the non-amplified group), but the difference was not statistically significant, int-2 amplification was not associated with increased risk of relapse, whereas the prognostic value of the c-myc amplification could not be evaluated.
对100例挪威淋巴结阴性乳腺癌患者的原发性肿瘤进行了c-erbB-2、int-2和c-myc原癌基因扩增检测。分别在12.1%(99例中的12例)、8.6%(93例中的8例)和1.1%(89例中的1例)的样本中发现了c-erbB-2、int-2和c-myc扩增。所有c-erbB-2扩增的肿瘤均为导管型,所有int-2扩增的肿瘤雌激素受体均为阳性。未发现基因扩增与临床或组织病理学参数之间存在其他显著或临界显著的关联。c-erbB-2基因扩增的患者复发更频繁(c-erbB-2扩增患者的复发率为33.3%,而非扩增组为20.7%),但差异无统计学意义,int-2扩增与复发风险增加无关,而c-myc扩增的预后价值无法评估。