Detection of K-ras point mutations at codon 12 in pure pancreatic juice for the diagnosis of pancreatic cancer by PCR-RFLP analysis

被引:61
作者
Watanabe, H
Sawabu, N
Songur, Y
Yamaguchi, Y
Yamakawa, O
Satomura, Y
Ohta, H
Motoo, Y
Okai, T
Wakabayashi, T
机构
[1] KANAZAWA UNIV,CANC RES INST,DEPT INTERNAL MED,KANAZAWA,ISHIKAWA 921,JAPAN
[2] KANAZAWA SAISEIKAI HOSP,DEPT GASTROENTEROL,KANAZAWA,ISHIKAWA,JAPAN
关键词
K-ras mutation at codon 12; pancreatic juice; pancreatic cancer; DNA diagnostic test; polymerase chain reaction (PCR); restriction fragment length polymorphism (RFLP);
D O I
10.1097/00006676-199601000-00003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The present study was undertaken to detect K-ras point mutations at codon 12 in pure pancreatic juice (PPJ) for the diagnosis of pancreatic cancer (PC) using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. PPJ was collected through a cannula under a duodenal fiberscope from 26 patients with PC and 32 patients with chronic pancreatitis (CP). DNA was extracted from PPJ and was used as the template for PCR. Analysis of PPJ by PCR-RFLP with BstNI revealed that the incidence of K-ras point mutations at codon 12 was 81% (21/26) in patients with PC and 6% (2/32) in those with CP. With reference to the location of PC, the incidence of K-ras mutations was 79% (11/14) in the head, 86% (6/7) in the body, and 80% (4/5) in the tail of the pancreas. The incidence of K-ras mutants was 50% (1/2) in tumor size 1 (TS1; less than or equal to 2.0 cm in size), 71% (5/7) in TS2 (2.1 to less than or equal to 4.0 cm), 89% (8/9) in TS3 (4.1 to less than or equal to 6.0 cm), and 88% (7/8) in TS4 (>6.1 cm). These results suggested that analysis of K-ras point mutations at codon 12 in PPJ using the PCR-RFLP method is a promising new genetic test for the diagnosis of PC.
引用
收藏
页码:18 / 24
页数:7
相关论文
共 36 条
[1]   MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES [J].
ALMOGUERA, C ;
SHIBATA, D ;
FORRESTER, K ;
MARTIN, J ;
ARNHEIM, N ;
PERUCHO, M .
CELL, 1988, 53 (04) :549-554
[2]   PROGNOSTIC VALUE OF P53 OVEREXPRESSION AND C-KI-RAS GENE-MUTATIONS IN COLORECTAL-CANCER [J].
BELL, SM ;
SCOTT, N ;
CROSS, D ;
SAGAR, P ;
LEWIS, FA ;
BLAIR, GE ;
TAYLOR, GR ;
DIXON, MF ;
QUIRKE, P .
GASTROENTEROLOGY, 1993, 104 (01) :57-64
[3]   PREVALENCE OF RAS GENE-MUTATIONS IN HUMAN COLORECTAL CANCERS [J].
BOS, JL ;
FEARON, ER ;
HAMILTON, SR ;
VERLAANDEVRIES, M ;
VANBOOM, JH ;
VANDEREB, AJ ;
VOGELSTEIN, B .
NATURE, 1987, 327 (6120) :293-297
[4]   RAPID ISOLATION OF EUKARYOTIC DNA [J].
BOWTELL, DDL .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (02) :463-465
[5]   MAXIMIZING SENSITIVITY AND SPECIFICITY OF PCR BY PREAMPLIFICATION HEATING [J].
DAQUILA, RT ;
BECHTEL, LJ ;
VIDELER, JA ;
ERON, JJ ;
GORCZYCA, P ;
KAPLAN, JC .
NUCLEIC ACIDS RESEARCH, 1991, 19 (13) :3749-3749
[6]   DETECTION OF HIGH-INCIDENCE OF K-RAS ONCOGENES DURING HUMAN-COLON TUMORIGENESIS [J].
FORRESTER, K ;
ALMOGUERA, C ;
HAN, KY ;
GRIZZLE, WE ;
PERUCHO, M .
NATURE, 1987, 327 (6120) :298-303
[7]   HIGH-FREQUENCY OF KI-RAS CODON-12 MUTATIONS IN PANCREATIC ADENOCARCINOMAS [J].
GRUNEWALD, K ;
LYONS, J ;
FROHLICH, A ;
FEICHTINGER, H ;
WEGER, RA ;
SCHWAB, G ;
JANSSEN, JWG ;
BARTRAM, CR .
INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (06) :1037-1041
[8]   DETECTION OF MINORITY POINT MUTATIONS BY MODIFIED PCR TECHNIQUE - A NEW APPROACH FOR A SENSITIVE DIAGNOSIS OF TUMOR-PROGRESSION MARKERS [J].
HALIASSOS, A ;
CHOMEL, JC ;
GRANDJOUAN, S ;
KRUH, J ;
KAPLAN, JC ;
KITZIS, A .
NUCLEIC ACIDS RESEARCH, 1989, 17 (20) :8093-8099
[9]   A RAPID METHOD FOR THE PURIFICATION OF DNA FROM BLOOD [J].
JEANPIERRE, M .
NUCLEIC ACIDS RESEARCH, 1987, 15 (22) :9611-9612
[10]  
KAHN SM, 1991, ONCOGENE, V6, P1079