Miki H, Matsumoto S, Harada H, Mori S, Haba R, Ochi K, Kobayashi S, Ohmori M
Department of Pathology, Kagawa Medical School, Japan.
Int J Pancreatol. 1993 Oct;14(2):145-8. doi: 10.1007/BF02786120.
Cytological diagnosis of pancreatic carcinoma sometimes poses difficulties in distinguishing malignant from benign cells. Recent molecular study of pancreatic carcinoma has revealed a very high incidence of a point mutation of the c-Ki-ras oncogene at codon 12 in this neoplasm. To take advantage of this technique for the diagnosis of pancreatic carcinoma, we attempted to amplify the c-Ki-ras gene from endoscopically obtained pancreatic juice by isolation of DNA and polymerase chain reaction (PCR) coupled with restriction fragment length polymorphism (RFLP). PCR was possible in approx 70% of the cases. A point mutation was nonradioisotopically detected in 4 of 6 pancreatic carcinomas and in one intraductal papillary neoplasm, whereas no mutation was detected in other cases. Thus, this method was thought to be useful for the diagnosis of pancreatic carcinoma.
胰腺癌的细胞学诊断有时难以区分恶性细胞和良性细胞。最近对胰腺癌的分子研究显示,在这种肿瘤中,c-Ki-ras癌基因第12密码子处的点突变发生率非常高。为利用该技术诊断胰腺癌,我们尝试通过DNA分离、聚合酶链反应(PCR)以及限制性片段长度多态性(RFLP),从内镜获取的胰液中扩增c-Ki-ras基因。约70%的病例能够进行PCR。在6例胰腺癌中的4例以及1例导管内乳头状肿瘤中检测到非放射性标记的点突变,而其他病例未检测到突变。因此,该方法被认为对胰腺癌的诊断有用。