MMTV-induced mammary tumorigenesis: gene discovery, progression to malignancy and cellular pathways

被引:139
作者
Callahan, R [1 ]
Smith, GH [1 ]
机构
[1] NCI, Tumor Immunol & Biol Lab, Bethesda, MD 20892 USA
关键词
MMTV; Wnt; Fgf; notch; elF3p48/INT6;
D O I
10.1038/sj.onc.1203276
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 study of the mouse mammary tumor virus (MMTV) has provided important insights into the mechanisms of gene transcription regulation by steroid hormones, the mode of action of heritable super antigens and the progressive nature of neoplastic transformation in the mammary gland, Here we describe the current situation with respect to the latter aspect of MMTV biology and the prospects for further advance in our understanding of breast cancer in humans that may be expected from a continued study of MMTV-induced mammary neoplasia, MMTV is a heritable somatic mutagen whose target range is limited, Commonly, the tumorigenic capacity of MMTV is restricted to mammary gland, whereas infection is found in a variety of cell types, In order to replicate, proviral DNA must be inserted into the cell DNA and cell division is required to fix the mutation. Yet only in the mammary epithelium does this lead to neoplastic transformation. This suggests a unique relationship between MMTV and mammary epithelium. In evaluating this relationship, we and others have discovered genes and potential gene pathways that are pertinent in mammary differentiation and neoplasia, In addition, the clonal nature of these progressive events from normal to malignant phenotype has become increasingly clear, The weight of these observations compel us to conclude that mammary neoplasms arise from multipotent mammary epithelial cells through a process of acquired mutations that are reflected in the increasingly malignant nature of the population of progeny produced by these damaged stem cells.
引用
收藏
页码:992 / 1001
页数:10
相关论文
共 123 条
[1]   BIOLOGICAL STUDIES ON THE MAMMARY TUMOR INCITER IN MICE [J].
ANDERVONT, HB .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1952, 54 (06) :1004-1011
[2]  
ANDERVONT HB, 1962, J NATL CANCER I, V28, P1153
[3]   NOTCH SIGNALING [J].
ARTAVANISTSAKONAS, S ;
MATSUNO, K ;
FORTINI, ME .
SCIENCE, 1995, 268 (5208) :225-232
[4]   The translation initiation factor eIF3-p48 subunit is encoded by int-6, a site of frequent integration by the mouse mammary tumor virus genome [J].
Asano, K ;
Merrick, WC ;
Hershey, JWB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (38) :23477-23480
[5]   Interaction between wingless and notch signaling pathways mediated by dishevelled [J].
Axelrod, JD ;
Matsuno, K ;
ArtavanisTsakonas, S ;
Perrimon, N .
SCIENCE, 1996, 271 (5257) :1826-1832
[6]   THE FGF FAMILY OF GROWTH-FACTORS AND ONCOGENES [J].
BASILICO, C ;
MOSCATELLI, D .
ADVANCES IN CANCER RESEARCH, 1992, 59 :115-165
[7]   GENETIC ALTERATIONS IN BREAST-CANCER [J].
BIECHE, I ;
LIDEREAU, R .
GENES CHROMOSOMES & CANCER, 1995, 14 (04) :227-251
[8]   Some possible effects of nursing on the mammary gland tumor incidence in mice. [J].
Bittner, JJ .
SCIENCE, 1936, 84 :162-162
[9]   AN ONCOGENE ISOLATED BY TRANSFECTION OF KAPOSIS-SARCOMA DNA ENCODES A GROWTH-FACTOR THAT IS A MEMBER OF THE FGF FAMILY [J].
BOVI, PD ;
CURATOLA, AM ;
KERN, FG ;
GRECO, A ;
ITTMANN, M ;
BASILICO, C .
CELL, 1987, 50 (05) :729-737
[10]   MMTV-induced mutations in mouse mammary tumors: Their potential relevance to human breast cancer [J].
Callahan, R .
BREAST CANCER RESEARCH AND TREATMENT, 1996, 39 (01) :33-44