DIFFERENTIAL TRANSFORMATION OF MAMMARY EPITHELIAL-CELLS BY WNT GENES

被引:289
作者
WONG, GT [1 ]
GAVIN, BJ [1 ]
MCMAHON, AP [1 ]
机构
[1] ROCHE INST MOLEC BIOL, NUTLEY, NJ 07110 USA
关键词
D O I
10.1128/MCB.14.9.6278
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mouse Wnt family includes at least 10 genes that encode structurally related secreted glycoproteins. Wnt-1 and Wnt-3 were originally identified as oncogenes activated by the insertion of mouse mammary tumor virus in virus-induced mammary adenocarcinomas, although they are not expressed in the normal mammary gland. However, five other Wnt genes are differentially expressed during development of adult mammary tissue, suggesting that they mag play distinct roles in various phases of mammary gland growth and development. Induction of transformation by Wnt-1 and Wnt-3 may be due to interference with these normal regulatory events; however, there is no direct evidence for this hypothesis. We have tested Wnt family members for the ability to induce transformation of cultured mammary cells. The results demonstrate that the Wnt gene family can be divided into three groups depending on their ability to induce morphological transformation and altered growth characteristics of the C57MG mammary epithelial cell line. Wnt-1, Wnt-3A, and Wnt-7A were highly transforming and induced colonies which formed and shed balls of cells, Wnt-2, Wnt-5B, and Wnt-7B also induced transformation but with a lower frequency and an apparent decrease in saturation density. In contrast, Wnt-6 and two other family members which are normally expressed in C57MG cells, Wnt-4 and Wnt-5A, failed to induce transformation. These data demonstrate that the Wnt genes have distinct effects on cell growth and should not be regarded as functionally equivalent.
引用
收藏
页码:6278 / 6286
页数:9
相关论文
共 59 条
  • [1] BLASBAND A, 1992, ONCOGENE, V7, P153
  • [2] INSULIN IS ESSENTIAL FOR ACCUMULATION OF CASEIN MESSENGER-RNA IN MOUSE MAMMARY EPITHELIAL-CELLS
    BOLANDER, FF
    NICHOLAS, KR
    VANWYK, JJ
    TOPPER, YJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09): : 5682 - 5684
  • [3] GROWTH-CONTROL AND DIFFERENTIATION IN MAMMARY EPITHELIAL-CELLS
    BORELLINI, F
    OKA, T
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1989, 80 : 85 - 99
  • [4] THE PROTOONCOGENE INT-1 ENCODES A SECRETED PROTEIN ASSOCIATED WITH THE EXTRACELLULAR-MATRIX
    BRADLEY, RS
    BROWN, AMC
    [J]. EMBO JOURNAL, 1990, 9 (05) : 1569 - 1575
  • [5] A RETROVIRUS VECTOR EXPRESSING THE PUTATIVE MAMMARY ONCOGENE INT-1 CAUSES PARTIAL TRANSFORMATION OF A MAMMARY EPITHELIAL-CELL LINE
    BROWN, AMC
    WILDIN, RS
    PRENDERGAST, TJ
    VARMUS, HE
    [J]. CELL, 1986, 46 (07) : 1001 - 1009
  • [6] LOCALIZATION AND QUANTIFICATION OF WNT-2 GENE-EXPRESSION IN MOUSE MAMMARY DEVELOPMENT
    BUHLER, TA
    DALE, TC
    KIEBACK, C
    HUMPHREYS, RC
    ROSEN, JM
    [J]. DEVELOPMENTAL BIOLOGY, 1993, 155 (01) : 87 - 96
  • [7] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [8] INHIBITION OF MOUSE MAMMARY DUCTAL MORPHOGENESIS AND DOWN-REGULATION OF THE EGF RECEPTOR BY EPIDERMAL GROWTH-FACTOR
    COLEMAN, S
    DANIEL, CW
    [J]. DEVELOPMENTAL BIOLOGY, 1990, 137 (02) : 425 - 433
  • [9] TGF-BETA-1-INDUCED INHIBITION OF MOUSE MAMMARY DUCTAL GROWTH - DEVELOPMENTAL SPECIFICITY AND CHARACTERIZATION
    DANIEL, CW
    SILBERSTEIN, GB
    VANHORN, K
    STRICKLAND, P
    ROBINSON, S
    [J]. DEVELOPMENTAL BIOLOGY, 1989, 135 (01) : 20 - 30
  • [10] EDWARDS PAW, 1992, ONCOGENE, V7, P2041