Mammary hyperplasia and carcinoma in MMTV-cyclin D1 transgenic mice. 1994

T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
Department of Medicine, Massachusetts General Hospital, Boston 02114.

Physical associations between cyclins, viral oncogenes and tumour suppressor genes imply a central role for cyclins in growth control. Cyclin D1 was identified as a candidate oncogene (PRAD1) in tumour-specific DNA rearrangements and is suspected to be a contributor to several types of neoplasms including breast cancer. Cyclin D1 also rescues G1 cyclin-defective Saccharomyces cerevisiae, and is a growth-regulated gene. Despite evidence suggesting that cyclin D1 is an oncogene, its ability to transform cells directly in culture remains controversial. 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.

UI MeSH Term Description Entries
D006965 Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. Hyperplasias
D008297 Male Males
D008321 Mammary Glands, Animal MAMMARY GLANDS in the non-human MAMMALS. Mammae,Udder,Animal Mammary Glands,Animal Mammary Gland,Mammary Gland, Animal,Udders
D008324 Mammary Tumor Virus, Mouse The type species of BETARETROVIRUS commonly latent in mice. It causes mammary adenocarcinoma in a genetically susceptible strain of mice when the appropriate hormonal influences operate. Bittner Virus,Mammary Cancer Virus,Mouse mammary tumor virus,Mammary Tumor Viruses, Mouse
D008325 Mammary Neoplasms, Experimental Experimentally induced mammary neoplasms in animals to provide a model for studying human BREAST NEOPLASMS. Experimental Mammary Neoplasms,Neoplasms, Experimental Mammary,Experimental Mammary Neoplasm,Mammary Neoplasm, Experimental,Neoplasm, Experimental Mammary
D008807 Mice, Inbred BALB C An inbred strain of mouse that is widely used in IMMUNOLOGY studies and cancer research. BALB C Mice, Inbred,BALB C Mouse, Inbred,Inbred BALB C Mice,Inbred BALB C Mouse,Mice, BALB C,Mouse, BALB C,Mouse, Inbred BALB C,BALB C Mice,BALB C Mouse
D008822 Mice, Transgenic Laboratory mice that have been produced from a genetically manipulated EGG or EMBRYO, MAMMALIAN. Transgenic Mice,Founder Mice, Transgenic,Mouse, Founder, Transgenic,Mouse, Transgenic,Mice, Transgenic Founder,Transgenic Founder Mice,Transgenic Mouse
D009857 Oncogenes Genes whose gain-of-function alterations lead to NEOPLASTIC CELL TRANSFORMATION. They include, for example, genes for activators or stimulators of CELL PROLIFERATION such as growth factors, growth factor receptors, protein kinases, signal transducers, nuclear phosphoproteins, and transcription factors. A prefix of "v-" before oncogene symbols indicates oncogenes captured and transmitted by RETROVIRUSES; the prefix "c-" before the gene symbol of an oncogene indicates it is the cellular homolog (PROTO-ONCOGENES) of a v-oncogene. Transforming Genes,Oncogene,Transforming Gene,Gene, Transforming,Genes, Transforming
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
June 1990, Cell,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
March 1997, The Journal of pathology,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
January 2002, Breast cancer research : BCR,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
November 1998, Oncogene,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
July 2003, Oncogene,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
July 2001, Cancer research,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
January 2002, Oncogene,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
April 1998, The Journal of pathology,
T C Wang, and R D Cardiff, and L Zukerberg, and E Lees, and A Arnold, and E V Schmidt
January 2010, Oncogene,
Copied contents to your clipboard!