Hajj C, Akoum R, Bradley E, Paquin F, Ayoub J
Institut du Cancer de Montréal, Hôpital Notre-Dame, Québec, Canada.
Cancer. 1990 Aug 15;66(4):733-9. doi: 10.1002/1097-0142(19900815)66:4<733::aid-cncr2820660422>3.0.co;2-c.
DNA from tumor samples of 54 patients with operable non-small cell lung cancer (NSCLC) was analyzed to determine whether proto-oncogene alterations could be correlated with the clinical behavior of lung cancer. Among seven proto-oncogenes tested, changes in the copy number of Ha-ras, c-myc and c-raf-1 were found in only seven tumors. Most of them were epidermoid carcinomas without lymph node involvement (N0). In spite of a localized disease with complete surgical resection, six of these patients relapsed within a mean disease-free interval (DFI) of only 6.5 months. There is a significant correlation between DNA alterations at proto-oncogene loci and clinical relapse within 12 months of surgical resection (P less than 0.025).
对54例可手术切除的非小细胞肺癌(NSCLC)患者的肿瘤样本DNA进行分析,以确定原癌基因改变是否与肺癌的临床行为相关。在检测的7个原癌基因中,仅在7个肿瘤中发现Ha-ras、c-myc和c-raf-1的拷贝数变化。其中大多数为无淋巴结转移(N0)的表皮样癌。尽管疾病局限且手术完全切除,但这些患者中有6例在平均无病生存期(DFI)仅6.5个月内复发。原癌基因位点的DNA改变与手术切除后12个月内的临床复发之间存在显著相关性(P<0.025)。