MAMMARY HYPERPLASIA AND CARCINOMA IN MMTV-CYCLIN D1 TRANSGENIC MICE

被引:883
作者
WANG, TC
CARDIFF, RD
ZUKERBERG, L
LEES, E
ARNOLD, A
SCHMIDT, EV
机构
[1] MASSACHUSETTS GEN HOSP, CTR CANC, BOSTON, MA 02129 USA
[2] UNIV CALIF DAVIS, SCH MED, DEPT PATHOL, DAVIS, CA 95616 USA
[3] MASSACHUSETTS GEN HOSP, DEPT MED, ENDOCRINE ONCOL LAB, BOSTON, MA 02114 USA
[4] MASSACHUSETTS GEN HOSP, CTR CANC, BOSTON, MA 02114 USA
[5] MASSACHUSETTS GEN HOSP, DEPT PATHOL, BOSTON, MA 02114 USA
[6] MASSACHUSETTS GEN HOSP, CHILDRENS SERV, BOSTON, MA 02129 USA
[7] MASSACHUSETTS GEN HOSP, DEPT MED, GASTROINTESTINAL UNIT, BOSTON, MA 02114 USA
关键词
D O I
10.1038/369669a0
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
Physical associations between cyclins, viral oncogenes and tumour suppressor genes imply a central role for cyclins in growth control(1,2). Cyclin D1 was identified as a candidate oncogene (PRAD1) in tumour-specific DNA rearrangements(3,4) and is suspected to be a contributor to several types of neoplasms including breast cancer(5,6). Cyclin D1 also rescues G1 cyclin-defective Saccharomyces cerevisiae(7), and is a growth-regulated genes. Despite evidence suggesting that cyclin D1 is an oncogene, its ability to transform cells directly in culture remains controversial(9-16). To evaluate its potential to deregulate growth in vivo in a physiologically relevant tissue we overexpressed cyclin D1 in mammary cells in transgenic mice. We report here that overexpression of cyclin D1 resulted in abnormal mammary cell proliferation including the development of mammary adenocarcinomas. We conclude that overexpression of cyclin D1 deregulates cell proliferation and can induce tumorigenic changes in mammary tissues, suggesting that cyclin D1 indeed plays an important oncogenic role in breast cancer.
引用
收藏
页码:669 / 671
页数:3
相关论文
共 26 条
  • [1] CYCLIN D1 IS A NUCLEAR-PROTEIN REQUIRED FOR CELL-CYCLE PROGRESSION IN G(1)
    BALDIN, V
    LUKAS, J
    MARCOTE, MJ
    PAGANO, M
    DRAETTA, G
    [J]. GENES & DEVELOPMENT, 1993, 7 (05) : 812 - 821
  • [2] ASSOCIATION OF INT2/HST1 COAMPLIFICATION IN PRIMARY BREAST-CANCER WITH HORMONE-DEPENDENT PHENOTYPE AND POOR PROGNOSIS
    BORG, A
    SIGURDSSON, H
    CLARK, GM
    FERNO, M
    FUQUA, SAW
    OLSSON, H
    KILLANDER, D
    MCGURIE, WL
    [J]. BRITISH JOURNAL OF CANCER, 1991, 63 (01) : 136 - 142
  • [3] CHARACTERIZATION AND CHROMOSOME ASSIGNMENT OF THE HUMAN HOMOLOG OF INT-2, A POTENTIAL PROTOONCOGENE
    CASEY, G
    SMITH, R
    MCGILLIVRAY, D
    PETERS, G
    DICKSON, C
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (02) : 502 - 510
  • [4] INTERACTION BETWEEN HUMAN CYCLIN-A AND ADENOVIRUS E1A-ASSOCIATED P107 PROTEIN
    FAHA, B
    EWEN, ME
    TSAI, LH
    LIVINGSTON, DM
    HARLOW, E
    [J]. SCIENCE, 1992, 255 (5040) : 87 - 90
  • [5] FUNCTION OF A HUMAN CYCLIN GENE AS AN ONCOGENE
    HINDS, PW
    DOWDY, SF
    EATON, EN
    ARNOLD, A
    WEINBERG, RA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) : 709 - 713
  • [6] REGULATION OF RETINOBLASTOMA PROTEIN FUNCTIONS BY ECTOPIC EXPRESSION OF HUMAN CYCLINS
    HINDS, PW
    MITTNACHT, S
    DULIC, V
    ARNOLD, A
    REED, SI
    WEINBERG, RA
    [J]. CELL, 1992, 70 (06) : 993 - 1006
  • [7] JIANG W, 1993, ONCOGENE, V8, P3447
  • [8] LAMMIE GA, 1991, CANCER CELL-MON REV, V3, P413
  • [9] LAMMIE GA, 1991, ONCOGENE, V6, P439
  • [10] LOVEC H, 1994, ONCOGENE, V9, P323