FREQUENT MUTATIONS OF CDKN2 IN PRIMARY PANCREATIC ADENOCARCINOMAS

被引:80
作者
BARTSCH, D
SHEVLIN, DW
TUNG, WS
KISKER, O
WELLS, SA
GOODFELLOW, PJ
机构
[1] WASHINGTON UNIV,SCH MED,DEPT SURG,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT PATHOL,ST LOUIS,MO 63110
[3] UNIV MARBURG,DEPT SURG,W-3550 MARBURG,GERMANY
关键词
D O I
10.1002/gcc.2870140306
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The gene encoding the cell-cycle regulatory protein p16, CDKN2, is localized on chromosome band 9p21. CDKN2 is frequently deleted or mutated in a variety of tumor cell lines, including pancreatic cancer cell lines and xenografts, as well as in some primary tumors. We examined 32 primary pancreatic adenocarcinomas for CDKN2 mutations and for loss of heterozygosity of 9p21 sequences to assess the role of CDKN2 in pancreatic carcinogenesis. Single-strand conformation variant analysis (SSCV) and direct sequencing of the variants revealed somatic CDKN2 mutations in 11 of 32 tumors (five frame-shift mutations, five nonsense mutations, and one missense mutation). One tumor appeared to be characterized by homozygous deletion of CDKN2. These results suggest that CDKN2 plays an important role during tumorigenesis or tumor progression in a significant proportion of pancreatic adenocarcinomas. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 38 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] STEPWISE TRANSFORMATION OF PRIMARY THYROID EPITHELIAL-CELLS BY A MUTANT HA-RAS ONCOGENE - AN INVITRO MODEL OF TUMOR PROGRESSION
    BURNS, JS
    BLAYDES, JP
    WRIGHT, PA
    LEMOINE, L
    BOND, JA
    WILLIAMS, ED
    WYNFORDTHOMAS, D
    [J]. MOLECULAR CARCINOGENESIS, 1992, 6 (02) : 129 - 139
  • [3] RATES OF P16(MTS1) MUTATIONS IN PRIMARY TUMORS WITH 9P LOSS
    CAIRNS, P
    MAO, L
    MERLO, A
    LEE, DJ
    SCHWAB, D
    EBY, Y
    TOKINO, K
    VANDERRIET, P
    BLAUGRUND, JE
    SIDRANSKY, D
    [J]. SCIENCE, 1994, 265 (5170) : 415 - 416
  • [4] FREQUENT SOMATIC MUTATIONS AND HOMOZYGOUS DELETIONS OF THE P16 (MTS1) GENE IN PANCREATIC ADENOCARCINOMA
    CALDAS, C
    HAHN, SA
    DACOSTA, LT
    REDSTON, MS
    SCHUTTE, M
    SEYMOUR, AB
    WEINSTEIN, CL
    HRUBAN, RH
    YEO, CJ
    KERN, SE
    [J]. NATURE GENETICS, 1994, 8 (01) : 27 - 32
  • [5] CALDAS C, 1994, CANCER RES, V54, P3568
  • [6] MUTATIONS IN THE RET PROTOONCOGENE ARE ASSOCIATED WITH MEN 2A AND FMTC
    DONISKELLER, H
    DOU, SS
    CHI, D
    CARLSON, KM
    TOSHIMA, K
    LAIRMORE, TC
    HOWE, JR
    MOLEY, JF
    GOODFELLOW, P
    WELLS, SA
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (07) : 851 - 856
  • [7] P53-DEPENDENT INHIBITION OF CYCLIN-DEPENDENT KINASE-ACTIVITIES IN HUMAN FIBROBLASTS DURING RADIATION-INDUCED G1 ARREST
    DULIC, V
    KAUFMANN, WK
    WILSON, SJ
    TLSTY, TD
    LEES, E
    HARPER, JW
    ELLEDGE, SJ
    REED, SI
    [J]. CELL, 1994, 76 (06) : 1013 - 1023
  • [8] CLINICAL IMPLICATIONS OF THE P53 TUMOR-SUPPRESSOR GENE
    HARRIS, CC
    HOLLSTEIN, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (18) : 1318 - 1327
  • [9] SOMATIC MUTATIONS OF THE MTS (MULTIPLE TUMOR-SUPPRESSOR)-1 CDK41 (CYCLIN-DEPENDENT KINASE-4 INHIBITOR) GENE IN HUMAN PRIMARY NONSMALL CELL LUNG CARCINOMAS
    HAYASHI, N
    SUGIMOTO, Y
    TSUCHIYA, E
    OGAWA, M
    NAKAMURA, Y
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 202 (03) : 1426 - 1430
  • [10] HRUBAN RH, 1993, AM J PATHOL, V143, P545