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PMID: 2898299 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Single-step induction of mammary adenocarcinoma in transgenic mice bearing the activated c-neu oncogene.

Cell ·Vol. 54 ·No. 1 ·1988-07-01 ·Pages 105-15

Muller WJ, Sinn E, Pattengale PK, Wallace R, Leder P

Abstract

We have used transgenic mice that carry an activated c-neu oncogene driven by a mouse mammary tumor virus (MMTV) promoter to assess the stepwise progression of carcinogenesis in mammary epithelium. Unlike the stochastic occurrence of solitary mammary tumors in transgenic mice bearing the MMTV/c-myc or the MMTV/v-Ha-ras oncogenes, transgenic mice uniformly expressing the MMTV/c-neu gene develop mammary adenocarcinomas that involve the entire epithelium in each gland. Because these tumors arise synchronously and are polyclonal in origin, expression of the activated c-neu oncogene appears to be sufficient to induce malignant transformation in this tissue in a single step. In contrast, expression of the c-neu transgene in the parotid gland or epididymis leads to benign, bilateral epithelial hypertrophy and hyperplasia which does not progress to full malignant transformation during the observation period. These results indicate that the combination of activated oncogene and tissue context are major determinants of malignant progression and that expression of the activated form of c-neu in the mammary epithelium has particularly deleterious consequences.

MeSH Terms
Adenocarcinoma/etiology,genetics Animals Cell Transformation, Neoplastic Epididymis/pathology Epithelium/pathology Female Gene Expression Regulation Hyperplasia Hypertrophy Male Mammary Glands, Animal/pathology Mammary Neoplasms, Experimental/etiology,genetics Mice Mice, Transgenic Oncogenes Organ Specificity Parotid Gland/pathology Phenotype Proto-Oncogene Proteins/genetics Receptor, ErbB-2
Chemicals
Proto-Oncogene Proteins Receptor, ErbB-2
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Muller W J
Harvard Medical School Department of Genetics, Boston, Massachusetts 02115.
Sinn E
Pattengale P K
Wallace R
Leder P
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1988-07-01
Pages
105-15
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · 5 T32 GM07196 · United States
NCI NIH HHS · CA-07968 · United States
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