DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1

被引:2078
作者
Hahn, SA
Schutte, M
Hoque, ATMS
Moskaluk, CA
daCosta, LT
Rozenblum, E
Weinstein, CL
Fischer, A
Yeo, CJ
Hruban, RH
Kern, SE
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT ONCOL,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT PATHOL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT SURG,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,SCH MED,GRAD PROGRAM HUMAN GENET & MOLEC BIOL,BALTIMORE,MD 21205
关键词
D O I
10.1126/science.271.5247.350
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
About 90 percent of human pancreatic carcinomas show allelic loss at chromosome 18q. To identify candidate tumor suppressor genes on 18q, a panel of pancreatic carcinomas were analyzed for convergent sites of homboygous deletion. Twenty-five of 84 tumors had homozygous deletions at 18q21.1, a site that excludes DCC (a candidate suppressor gene for colorectal cancer) and includes DPC4, a gene similar in sequence to a Drosophila melanogaster gene (Mad) implicated in a transforming growth factor-beta (TGF-beta)-like signaling pathway. Potentially inactivating mutations in DPC4 were identified in six of 27 pancreatic carcinomas that did not have homozygous deletions at 18q21.1. These results identify DPC4 as a candidate tumor suppressor gene whose inactivation may play a role in pancreatic and possibly other human cancers.
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页码:350 / 353
页数:4
相关论文
共 27 条
  • [1] ALEXANDROW MG, 1995, CANCER RES, V55, P1452
  • [2] 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
  • [3] THE MOLECULAR-GENETICS OF CANCER
    BISHOP, JM
    [J]. SCIENCE, 1987, 235 (4786) : 305 - 311
  • [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] THE DCC GENE - STRUCTURAL-ANALYSIS AND MUTATIONS IN COLORECTAL CARCINOMAS
    CHO, KR
    OLINER, JD
    SIMONS, JW
    HEDRICK, L
    FEARON, ER
    PREISINGER, AC
    HEDGE, P
    SILVERMAN, GA
    VOGELSTEIN, B
    [J]. GENOMICS, 1994, 19 (03) : 525 - 531
  • [6] CONE D, 1993, NATURE, V366, P698
  • [7] MOLECULAR-DETECTION OF DELETIONS INVOLVING BAND Q14 OF CHROMOSOME-13 IN RETINOBLASTOMAS
    DRYJA, TP
    RAPAPORT, JM
    JOYCE, JM
    PETERSEN, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) : 7391 - 7394
  • [8] IDENTIFICATION OF A CHROMOSOME-18Q GENE THAT IS ALTERED IN COLORECTAL CANCERS
    FEARON, ER
    CHO, KR
    NIGRO, JM
    KERN, SE
    SIMONS, JW
    RUPPERT, JM
    HAMILTON, SR
    PREISINGER, AC
    THOMAS, G
    KINZLER, KW
    VOGELSTEIN, B
    [J]. SCIENCE, 1990, 247 (4938) : 49 - 56
  • [9] A RADIATION HYBRID MAP OF HUMAN CHROMOSOME-18
    FRANCKE, U
    CHANG, E
    COMEAU, K
    GEIGL, EM
    GIACALONE, J
    LI, X
    LUNA, J
    MOON, A
    WELCH, S
    WILGENBUS, P
    [J]. CYTOGENETICS AND CELL GENETICS, 1994, 66 (03): : 196 - 213
  • [10] PROGRESSION OF COLORECTAL-CANCER IS ASSOCIATED WITH MULTIPLE TUMOR SUPPRESSOR GENE DEFECTS BUT INHIBITION OF TUMORIGENICITY IS ACCOMPLISHED BY CORRECTION OF ANY SINGLE DEFECT VIA CHROMOSOME TRANSFER
    GOYETTE, MC
    CHO, K
    FASCHING, CL
    LEVY, DB
    KINZLER, KW
    PARASKEVA, C
    VOGELSTEIN, B
    STANBRIDGE, EJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (03) : 1387 - 1395