Activated neu induces rapid tumor progression

被引:121
作者
Guy, CT
Cardiff, RD
Muller, WJ
机构
[1] MCMASTER UNIV,INST MOLEC BIOL & BIOTECHNOL,HAMILTON,ON L8S 4K1,CANADA
[2] UNIV CALIF DAVIS,SCH MED,DEPT PATHOL,DAVIS,CA 95616
关键词
D O I
10.1074/jbc.271.13.7673
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
Expression of the activated neu oncogene in transgenic mice has been associated with both the synchronous (single-step) and the stochastic (multistep) transformation of the mammary epithelium, To determine the basis for these conflicting observations, additional strains of transgenic mice carrying the activated neu oncogene under the transcriptional control of the mouse mammary tumor virus promoter/enhancer were produced. Activated neu transgene expression, as measured by in situ hybridization and ribonuclease protection assays, resulted in rapid conversion of the normal mammary epithelium to malignant phenotype in three independent strains of mice. Expression of the transgene in male mice led to epithelial hyperplasia of the epididymis and male infertility but not malignancy. These results indicate that tissue context is an important parameter in malignant progression and that expression of appropriate levels of activated neu is sufficient for rapid production of mammary tumors in transgenic mice.
引用
收藏
页码:7673 / 7678
页数:6
相关论文
共 35 条
[11]   EXPRESSION OF THE NEU PROTOONCOGENE IN THE MAMMARY EPITHELIUM OF TRANSGENIC MICE INDUCES METASTATIC DISEASE [J].
GUY, CT ;
WEBSTER, MA ;
SCHALLER, M ;
PARSONS, TJ ;
CARDIFF, RD ;
MULLER, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (22) :10578-10582
[12]   INDUCTION OF MAMMARY-TUMORS BY EXPRESSION OF POLYOMAVIRUS MIDDLE T-ONCOGENE - A TRANSGENIC MOUSE MODEL FOR METASTATIC DISEASE [J].
GUY, CT ;
CARDIFF, RD ;
MULLER, WJ .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (03) :954-961
[13]   AN IMPROVED INSITU HYBRIDIZATION METHOD FOR THE DETECTION OF CELLULAR RNAS IN DROSOPHILA TISSUE-SECTIONS AND ITS APPLICATION FOR LOCALIZING TRANSCRIPTS OF THE HOMEOTIC ANTENNAPEDIA GENE-COMPLEX [J].
HAFEN, E ;
LEVINE, M ;
GARBER, RL ;
GEHRING, WJ .
EMBO JOURNAL, 1983, 2 (04) :617-623
[14]   COOPERATION BETWEEN ONCOGENES [J].
HUNTER, T .
CELL, 1991, 64 (02) :249-270
[15]   TYROSINE PHOSPHORYLATION OF A 120-KILODALTON PP60SRC SUBSTRATE UPON EPIDERMAL GROWTH-FACTOR AND PLATELET-DERIVED GROWTH-FACTOR RECEPTOR STIMULATION AND IN POLYOMAVIRUS MIDDLE-T-ANTIGEN-TRANSFORMED CELLS [J].
KANNER, SB ;
REYNOLDS, AB ;
PARSONS, JT .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :713-720
[16]   AMPLIFICATION OF A NOVEL V-ERBB-RELATED GENE IN A HUMAN MAMMARY-CARCINOMA [J].
KING, CR ;
KRAUS, MH ;
AARONSON, SA .
SCIENCE, 1985, 229 (4717) :974-976
[17]  
LEMOINE NR, 1990, ONCOGENE, V5, P237
[18]  
LEVEBRE, 1991, MOL CELL BIOL, V11, P2529
[19]   EARLY AND MULTIFOCAL TUMORS IN BREAST, SALIVARY, HARDERIAN AND EPIDIDYMAL TISSUES DEVELOPED IN MMTY-NEU TRANSGENIC MICE [J].
LUCCHINI, F ;
SACCO, MG ;
HU, N ;
VILLA, A ;
BROWN, J ;
CESANO, L ;
MANGIARINI, L ;
RINDI, G ;
KINDL, S ;
SESSA, F ;
VEZZONI, P ;
CLERICI, L .
CANCER LETTERS, 1992, 64 (03) :203-209
[20]  
MELTON DA, 1984, NUCLEIC ACIDS RES, V5, P919