Clinical application of K-ras oncogene mutations in pancreatic carcinoma: Detection of micrometastases

被引:0
|
作者
Nomoto, S [1 ]
Nakao, A [1 ]
Ando, N [1 ]
Takeda, S [1 ]
Kasai, Y [1 ]
Inoue, S [1 ]
Kaneko, T [1 ]
Takagi, H [1 ]
机构
[1] Nagoya Univ, Sch Med, Dept Surg 2, Showa Ku, Nagoya, Aichi 466, Japan
来源
SEMINARS IN SURGICAL ONCOLOGY | 1998年 / 15卷 / 01期
关键词
pancreatic neoplasms genetics pathology mortality; ras genes; codon; adenocarcinoma/genetics/pathology/mortality; polymerase chain reaction; survival rate; restriction fragment length polymorphism; mutation; neoplasm invasiveness; CA-19-9; antigen; carcinoembryonic antigen; liver neoplasms; neoplasm metastasis; sensitivity and specificity; portal vein surgery; lymph node excision; lymphatic metastasis; staining;
D O I
10.1002/(SICI)1098-2388(199807/08)15:1<40::AID-SSU7>3.0.CO;2-W
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic adenocarcinomas are known to have a high incidence of K-ras gene mutation. We summarize our efforts to detect micrometastases through a search for mutated K-ras oncogene in liver tissues, peritoneal washings, para-aortic lymph nodes, and perioperative peripheral blood. Two-stage polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analysis were used to detect K-ras oncogene mutations at codon 12. Our results suggest that PCR/RFLP analysis is potentially highly sensitive for the detection of micrometastases in various tissues and might be of value in the diagnosis, treatment and follow-up of metastases in other organs with pancreatic adenocarcinoma. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:40 / 46
页数:7
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