Detection of Ki-ras and p53 gene mutations in tissue and pancreatic juice from pancreatic adenocarcinomas

被引:23
作者
Kondoh, S [1 ]
Kaino, M [1 ]
Okita, S [1 ]
Ryozawa, S [1 ]
Akiyama, T [1 ]
Okita, K [1 ]
机构
[1] Yamaguchi Univ, Sch Med, Dept Internal Med 1, Ube, Yamaguchi 755, Japan
关键词
pancreatic carcinomas; pure pancreatic juice; Ki-ras mutations; p53 tumor suppressor gene; PCR-SSCP analysis;
D O I
10.1007/s005350050101
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Pancreatic carcinomas have a high incidence of Ki-ras mutations, and the genetic change is thought to occur at an early stage in the carcinogenesis. The aim of this study was to evaluate the usefulness of detecting genetic mutations in pure pancreatic juice (PPJ). DNA was extracted from tissue specimens of pancreatic carcinomas and from cells in PPJ, and subjected to polymerase chain reaction-single-strand conformation polymorphism analysis. Two types of mobility shifts that indicate Ki-ms mutations were observed in 13 of the 20 (65%) tissue specimens obtained by operation or autopsy. Ten of 15 specimens (67%) of PPJ collected from patients with pancreatic carcinomas showed two types of mobility shifts. Conventional imaging techniques did not show two in 10 of these patients. PPJ from patients with non-cancerous pancreatic diseases showed no Ki-ras mutations. The p53 tumor suppressor gene, examined by PCR-SSCP analysis, was mutated in 8 of the 20 tissue specimens obtained by operation or autopsy (40%). The detection of Ki-ras and p53 mutations in PPJ could be useful for the early diagnosis of pancreatic carcinomas, especially for neoplastic lesions of the intraductal type.
引用
收藏
页码:390 / 396
页数:7
相关论文
共 32 条
[1]   GUANOSINE TRIPHOSPHATASE ACTIVATING PROTEIN (GAP) INTERACTS WITH THE P21-RAS EFFECTOR BINDING DOMAIN [J].
ADARI, H ;
LOWY, DR ;
WILLUMSEN, BM ;
DER, CJ ;
MCCORMICK, F .
SCIENCE, 1988, 240 (4851) :518-520
[2]   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
[3]  
BOS JL, 1989, CANCER RES, V49, P4682
[4]   A VARIATION IN THE STRUCTURE OF THE PROTEIN-CODING REGION OF THE HUMAN-P53 GENE [J].
BUCHMAN, VL ;
CHUMAKOV, PM ;
NINKINA, NN ;
SAMARINA, OP ;
GEORGIEV, GP .
GENE, 1988, 70 (02) :245-252
[5]  
CALDAS C, 1994, CANCER RES, V54, P3568
[6]  
FULTS D, 1992, CANCER RES, V52, P674
[7]  
Hanada K, 1996, CANCER, V77, P452, DOI 10.1002/(SICI)1097-0142(19960201)77:3<452::AID-CNCR5>3.0.CO
[8]  
2-M
[9]   TUMOR SUPPRESSOR GENES - NEW PROSPECTS FOR CANCER-RESEARCH [J].
HOLLINGSWORTH, RE ;
LEE, WH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (02) :91-96
[10]   P53 MUTATIONS IN HUMAN CANCERS [J].
HOLLSTEIN, M ;
SIDRANSKY, D ;
VOGELSTEIN, B ;
HARRIS, CC .
SCIENCE, 1991, 253 (5015) :49-53