MUTATION OF THE MXI1 GENE IN PROSTATE-CANCER

被引:193
作者
EAGLE, LR
YIN, XY
BROTHMAN, AR
WILLIAMS, BJ
ATKIN, NB
PROCHOWNIK, EV
机构
[1] CHILDRENS HOSP,DEPT PEDIAT,DIV HEMATOL ONCOL,PITTSBURGH,PA 15213
[2] UNIV UTAH,HLTH SCI CTR,DEPT PEDIAT,SALT LAKE CITY,UT 84132
[3] UNIV UTAH,HLTH SCI CTR,DEPT MED GENET,SALT LAKE CITY,UT 84132
[4] MT VERNON HOSP,DEPT CANC RES,NORTHWOOD HA6 2RN,MIDDX,ENGLAND
[5] UNIV PITTSBURGH,MED CTR,DEPT MOLEC GENET & BIOCHEM,PITTSBURGH,PA 15213
关键词
D O I
10.1038/ng0395-249
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Mxi1 protein negatively regulates Myc oncoprotein activity and thus potentially serves a tumour suppressor function. MXI1 maps to chromosome 10q24-q25, a region that is deleted in some cases of prostate cancer. We have detected mutations in the retained MXI1 alleles in four primary prostate tumours with 10q24-q25 deletions. Two tumours contained inactivating mutations, whereas two others contained the identical missense mutation. Fluorescence in situ hybridization also demonstrated loss of one MXI1 allele in an additional tumour lacking chromosome 10 abnormalities. MXI1 thus displays allelic loss and mutation in some cases of prostate cancer that may contribute to the pathogenesis or neoplastic evolution of this common malignancy.
引用
收藏
页码:249 / 255
页数:7
相关论文
共 54 条
  • [1] THE C-MYC ONCOGENE DRIVEN BY IMMUNOGLOBULIN ENHANCERS INDUCES LYMPHOID MALIGNANCY IN TRANSGENIC MICE
    ADAMS, JM
    HARRIS, AW
    PINKERT, CA
    CORCORAN, LM
    ALEXANDER, WS
    CORY, S
    PALMITER, RD
    BRINSTER, RL
    [J]. NATURE, 1985, 318 (6046) : 533 - 538
  • [2] ONCOGENIC ACTIVITY OF THE C-MYC PROTEIN REQUIRES DIMERIZATION WITH MAX
    AMATI, B
    BROOKS, MW
    LEVY, N
    LITTLEWOOD, TD
    EVAN, GI
    LAND, H
    [J]. CELL, 1993, 72 (02) : 233 - 245
  • [3] TRANSCRIPTIONAL ACTIVATION BY THE HUMAN C-MYC ONCOPROTEIN IN YEAST REQUIRES INTERACTION WITH MAX
    AMATI, B
    DALTON, S
    BROOKS, MW
    LITTLEWOOD, TD
    EVAN, GI
    LAND, H
    [J]. NATURE, 1992, 359 (6394) : 423 - 426
  • [4] SEQUENCE-SPECIFIC TRANSCRIPTIONAL ACTIVATION BY MYC AND REPRESSION BY MAX
    AMIN, C
    WAGNER, AJ
    HAY, N
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) : 383 - 390
  • [5] CYTOGENETIC SURVEY OF 32 CANCERS OF THE PROSTATE
    ARPS, S
    RODEWALD, A
    SCHMALENBERGER, B
    CARL, P
    BRESSEL, M
    KASTENDIECK, H
    [J]. CANCER GENETICS AND CYTOGENETICS, 1993, 66 (02) : 93 - 99
  • [6] CHROMOSOME STUDY OF 5 CANCERS OF THE PROSTATE
    ATKIN, NB
    BAKER, MC
    [J]. HUMAN GENETICS, 1985, 70 (04) : 359 - 364
  • [7] MAD - A HETERODIMERIC PARTNER FOR MAX THAT ANTAGONIZES MYC TRANSCRIPTIONAL ACTIVITY
    AYER, DE
    KRETZNER, L
    EISENMAN, RN
    [J]. CELL, 1993, 72 (02) : 211 - 222
  • [8] BAKER SJ, 1990, CANCER RES, V50, P7717
  • [9] BIRD ML, 1989, LEUKEMIA, V3, P182
  • [10] MAX - A HELIX-LOOP-HELIX ZIPPER PROTEIN THAT FORMS A SEQUENCE-SPECIFIC DNA-BINDING COMPLEX WITH MYC
    BLACKWOOD, EM
    EISENMAN, RN
    [J]. SCIENCE, 1991, 251 (4998) : 1211 - 1217