COOPERATIVE TUMORIGENIC EFFECTS OF GERMLINE MUTATIONS IN RB AND P53

被引:341
作者
WILLIAMS, BO
REMINGTON, L
ALBERT, DM
MUKAI, S
BRONSON, RT
JACKS, T
机构
[1] MIT,CTR CANC RES,DEPT BIOL,CAMBRIDGE,MA 02139
[2] UNIV WISCONSIN,DEPT OPHTHALMOL,MADISON,WI 53792
[3] HARVARD UNIV,SCH MED,MASSACHUSETTS EYE & EAR INFIRM,DEPT OPHTHALMOL,BOSTON,MA 02114
[4] TUFTS UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02111
[5] TUFTS UNIV,SCH VET MED,DEPT PATHOL,BOSTON,MA 02111
关键词
D O I
10.1038/ng0894-480
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The tumour suppressor genes Rb and p53 are mutated in several types of human cancer, and many tumour types carry mutations in both genes. To study how these genes normally function, we and others have created mouse strains with Rb and p53 mutations. Here we describe the phenotypic effects of combined germline mutations in these two tumour suppressor genes. Mice mutant for both genes have reduced viability and exhibit novel pathology including pinealoblastomas, islet cell tumours, bronchial epithelial hyperplasia and retinal dysplasia. These data indicate that mutations in Rb and p53 can cooperate in the transformation of certain cell types in the mouse.
引用
收藏
页码:480 / 484
页数:5
相关论文
共 59 条
[1]   BRIEF REPORT - IDIOPATHIC DIFFUSE HYPERPLASIA OF PULMONARY NEUROENDOCRINE CELLS AND AIRWAYS DISEASE [J].
AGUAYO, SM ;
MILLER, YE ;
WALDRON, JA ;
BOGIN, RM ;
SUNDAY, ME ;
STATON, GW ;
BEAM, WR ;
KING, TE .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (18) :1285-1288
[2]   BILATERAL RETINAL AND BRAIN-TUMORS IN TRANSGENIC MICE EXPRESSING SIMIAN VIRUS-40 LARGE T-ANTIGEN UNDER CONTROL OF THE HUMAN INTERPHOTORECEPTOR RETINOID-BINDING PROTEIN PROMOTER [J].
ALUBAIDI, MR ;
FONT, RL ;
QUIAMBAO, AB ;
KEENER, MJ ;
LIOU, GI ;
OVERBEEK, PA ;
BAEHR, W .
JOURNAL OF CELL BIOLOGY, 1992, 119 (06) :1681-1687
[3]   SUPPRESSION OF HUMAN COLORECTAL-CARCINOMA CELL-GROWTH BY WILD-TYPE-P53 [J].
BAKER, SJ ;
MARKOWITZ, S ;
FEARON, ER ;
WILLSON, JKV ;
VOGELSTEIN, B .
SCIENCE, 1990, 249 (4971) :912-915
[4]   REQUIREMENT FOR A FUNCTIONAL RB-1 GENE IN MURINE DEVELOPMENT [J].
CLARKE, AR ;
MAANDAG, ER ;
VANROON, M ;
VANDERLUGT, NMT ;
VANDERVALK, M ;
HOOPER, ML ;
BERNS, A ;
RIELE, HT .
NATURE, 1992, 359 (6393) :328-330
[5]   THYMOCYTE APOPTOSIS INDUCED BY P53-DEPENDENT AND INDEPENDENT PATHWAYS [J].
CLARKE, AR ;
PURDIE, CA ;
HARRISON, DJ ;
MORRIS, RG ;
BIRD, CC ;
HOOPER, ML ;
WYLLIE, AH .
NATURE, 1993, 362 (6423) :849-852
[6]  
CROOK T, 1991, ONCOGENE, V6, P873
[7]   GENETIC-BASIS FOR P53 OVEREXPRESSION IN HUMAN BREAST-CANCER [J].
DAVIDOFF, AM ;
HUMPHREY, PA ;
IGLEHART, JD ;
MARKS, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :5006-5010
[8]   WILD-TYPE P53 MEDIATES APOPTOSIS BY E1A, WHICH IS INHIBITED BY E1B [J].
DEBBAS, M ;
WHITE, E .
GENES & DEVELOPMENT, 1993, 7 (04) :546-554
[9]   P53 FUNCTIONS AS A CELL-CYCLE CONTROL PROTEIN IN OSTEOSARCOMAS [J].
DILLER, L ;
KASSEL, J ;
NELSON, CE ;
GRYKA, MA ;
LITWAK, G ;
GEBHARDT, M ;
BRESSAC, B ;
OZTURK, M ;
BAKER, SJ ;
VOGELSTEIN, B ;
FRIEND, SH .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (11) :5772-5781
[10]   MICE DEFICIENT FOR P53 ARE DEVELOPMENTALLY NORMAL BUT SUSCEPTIBLE TO SPONTANEOUS TUMORS [J].
DONEHOWER, LA ;
HARVEY, M ;
SLAGLE, BL ;
MCARTHUR, MJ ;
MONTGOMERY, CA ;
BUTEL, JS ;
BRADLEY, A .
NATURE, 1992, 356 (6366) :215-221