Yamashita K, Kida Y, Shinoda H, Kida M, Okayasu I
Department of Pathology, Kitasato University East Hospital, Kanagawa.
Jpn J Cancer Res. 1999 Feb;90(2):240-8. doi: 10.1111/j.1349-7006.1999.tb00739.x.
In order to clarify whether DNA analysis for K-ras mutation can be used to diagnose cancers in supernatants of pancreatic juice and bile, samples from 29 cases of pancreatic, biliary tract, gastric, and neuroendocrine carcinomas, 1 malignant lymphoma case, 2 cases of pancreatic adenoma, 9 cases of chronic pancreatitis and 21 other non-cancer cases were examined. Polymerase chain reaction (PCR) products for K-ras gene codons 2 to 97 of exons 1 and 2 were generated with 33/33 (100%) pancreatic juice and 41/41 (100%) bile samples. By the single strand conformation polymorphism (SSCP) method, point mutations were detected in the pancreatic juice or bile supernatants of 13/13 (100%) pancreas cancer cases, 5/14 (35.7%) biliary tract cancer cases, 1/2 (50.0%) pancreatic adenoma cases and 3/9 (33.3%) chronic pancreatitis cases. Direct sequencing confirmed identical point mutations in the supernatants, malignant cells of cytologic smears of pancreatic juice or bile and cancer tissues. The DNA analysis demonstrated the presence of K-ras point mutations in 3 cases of pancreatic carcinomas with false-negative cytologic diagnoses. This novel method allows simultaneous testing for genetic abnormalities in supernatants of pancreatic juice and bile, after removing cells for cytologic diagnosis and screening for pancreatic and biliary tract tumors.
为了阐明K-ras基因突变的DNA分析是否可用于诊断胰液和胆汁上清液中的癌症,对29例胰腺癌、胆管癌、胃癌和神经内分泌癌患者的样本、1例恶性淋巴瘤患者的样本、2例胰腺腺瘤患者的样本、9例慢性胰腺炎患者的样本以及21例其他非癌症患者的样本进行了检测。利用33份(100%)胰液样本和41份(100%)胆汁样本生成了K-ras基因第1和第2外显子2至97密码子的聚合酶链反应(PCR)产物。通过单链构象多态性(SSCP)方法,在13例(100%)胰腺癌患者的胰液或胆汁上清液、5例(35.7%)胆管癌患者的胰液或胆汁上清液、1例(50.0%)胰腺腺瘤患者的胰液或胆汁上清液以及3例(33.3%)慢性胰腺炎患者的胰液或胆汁上清液中检测到了点突变。直接测序证实了上清液、胰液或胆汁细胞学涂片的恶性细胞以及癌组织中存在相同的点突变。DNA分析显示,在3例细胞学诊断为假阴性的胰腺癌患者中存在K-ras点突变。这种新方法允许在去除用于细胞学诊断的细胞并筛查胰腺和胆管肿瘤后,同时检测胰液和胆汁上清液中的基因异常。