The nature and expression of int-5, a novel MMTV integration locus gene in carcinogen-induced mammary tumors

Vijayender Rao Durgam, Rajeshwar R Tekmal

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Our previous studies have resulted in the identification and cloning of int-5, a novel site of mouse mammary tumor virus (MMTV) integration, from BALB/c D2 precancerous hyperplastic alveolar nodules (HAN). This paper presents a detailed characterization of the int-5 locus from both D2 HAN and normal genome and expression of the unique gene from the MMTV integration site. Our results show that the cellular gene at the MMTV integration site in the int-5 locus is identical to the gene encoding aromatase (CYP19), a member of the cytochrome P-450 gene superfamily. MMTV is integrated within exon 10 in the 3′ untranslated region of the aromatase gene. This gene (int-5/aromatase) is expressed in normal mammary gland and overexpressed in mammary tumors. These results suggest that the overexpression of this gene may be responsible for mammary tumorigenesis. This is the first demonstration of integration of MMTV in a cellular gene that plays a role in hormone-dependent breast cancers.

Original languageEnglish (US)
Pages (from-to)179-186
Number of pages8
JournalCancer Letters
Volume87
Issue number2
DOIs
StatePublished - Dec 9 1994

Fingerprint

Virus Integration
Mouse mammary tumor virus
Carcinogens
Breast Neoplasms
Aromatase
Genes
3' Untranslated Regions
Human Mammary Glands
Cytochrome P-450 Enzyme System
Organism Cloning
Exons
Carcinogenesis
Breast
Genome
Hormones
Gene Expression

Keywords

  • Expression of int-5 in mammary cancer
  • Insertional mutation
  • int genes
  • MMTV integration locus

ASJC Scopus subject areas

  • Cancer Research
  • Molecular Biology
  • Oncology

Cite this

The nature and expression of int-5, a novel MMTV integration locus gene in carcinogen-induced mammary tumors. / Durgam, Vijayender Rao; Tekmal, Rajeshwar R.

In: Cancer Letters, Vol. 87, No. 2, 09.12.1994, p. 179-186.

Research output: Contribution to journalArticle

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