COMPARATIVE-ANALYSIS OF MUTATIONS IN THE P53 AND K-RAS GENES IN PANCREATIC-CANCER

被引:230
作者
BERROZPE, G
SCHAEFFER, J
PEINADO, MA
REAL, FX
PERUCHO, M
机构
[1] CALIF INST BIOL RES,LA JOLLA,CA
[2] UNIV AUTONOMA BARCELONA,INST MUNICIPAL INVEST MED,DEPT IMMUNOL,E-08003 BARCELONA,SPAIN
关键词
D O I
10.1002/ijc.2910580207
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mutations in codon 12 of K-ros occur in a high proportion of pancreatic cancer cases. Although there is evidence that p53 mutations also occur in this tumor, few studies have been reported to date and no comparison has been made of K-ras and p53 mutations in the same tissues. Single-strand conformation polymorphism and sequencing of the PCR products were used to determine mutations in p53 gene; to detect mutations in K-ros genes, the artificial restriction fragment length polymorphism (RFLP) approach was used. Eight out of 30 tissues from primary pancreas cancer and 3 of 4 samples from metastases showed p53 mutations. Fifteen out of 17 pancreatic cancer cell lines had p53 mutations. In 2 cases, the same p53 mutation was identified in the original tumor and in a tumor-derived cell line. The majority of p53 mutations were present in exons 5-9 of the gene. Mutations at codon 12 of the K-ras gene were identified in 23/32 pancreas cancer tissues and in 14/17 cell lines. There was no relationship between the types of mutation observed in the 2 genes. In conclusion, mutations in K-ros and p53 genes are common in pancreatic cancer. p53 mutations may occur more frequently in metastatic lesions than in primary tumors, although further work is necessary to investigate this point. (C) 1994 Wiley-Liss, Inc.
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页码:185 / 191
页数:7
相关论文
共 27 条
  • [1] MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES
    ALMOGUERA, C
    SHIBATA, D
    FORRESTER, K
    MARTIN, J
    ARNHEIM, N
    PERUCHO, M
    [J]. CELL, 1988, 53 (04) : 549 - 554
  • [2] ABNORMALITIES OF THE P53 TUMOR SUPPRESSOR GENE IN HUMAN PANCREATIC-CANCER
    BARTON, CM
    STADDON, SL
    HUGHES, CM
    HALL, PA
    OSULLIVAN, C
    KLOPPEL, G
    THEIS, B
    RUSSELL, RCG
    NEOPTOLEMOS, J
    WILLIAMSON, RCN
    LANE, DP
    LEMOINE, NR
    [J]. BRITISH JOURNAL OF CANCER, 1991, 64 (06) : 1076 - 1082
  • [3] SELECTIVE G-MUTATION TO T-MUTATION OF P53 GENE IN HEPATOCELLULAR-CARCINOMA FROM SOUTHERN AFRICA
    BRESSAC, B
    KEW, M
    WANDS, J
    OZTURK, M
    [J]. NATURE, 1991, 350 (6317) : 429 - 431
  • [4] CERNY WL, 1992, CANCER RES, V52, P4507
  • [5] CHIBA I, 1990, ONCOGENE, V5, P1603
  • [6] PROPERTIES OF P53 MUTATIONS DETECTED IN PRIMARY AND SECONDARY CERVICAL CANCERS SUGGEST MECHANISMS OF METASTASIS AND INVOLVEMENT OF ENVIRONMENTAL CARCINOGENS
    CROOK, T
    VOUSDEN, KH
    [J]. EMBO JOURNAL, 1992, 11 (11) : 3935 - 3940
  • [7] A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS
    FEARON, ER
    VOGELSTEIN, B
    [J]. CELL, 1990, 61 (05) : 759 - 767
  • [8] PRESENCE OF A POTENT TRANSCRIPTION ACTIVATING SEQUENCE IN THE P53 PROTEIN
    FIELDS, S
    JANG, SK
    [J]. SCIENCE, 1990, 249 (4972) : 1046 - 1049
  • [9] HIGH-FREQUENCY OF KI-RAS CODON-12 MUTATIONS IN PANCREATIC ADENOCARCINOMAS
    GRUNEWALD, K
    LYONS, J
    FROHLICH, A
    FEICHTINGER, H
    WEGER, RA
    SCHWAB, G
    JANSSEN, JWG
    BARTRAM, CR
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1989, 43 (06) : 1037 - 1041
  • [10] P53 MUTATIONS IN HUMAN CANCERS
    HOLLSTEIN, M
    SIDRANSKY, D
    VOGELSTEIN, B
    HARRIS, CC
    [J]. SCIENCE, 1991, 253 (5015) : 49 - 53