Accession Number : ADA323218
Title : Cloning and Characterizing Genes Involved in Monoterpene Induced Mammary Tumor Regression.
Descriptive Note : Annual rept. 1 Sep 95-31 Aug 96,
Corporate Author : WISCONSIN UNIV-MADISON
Personal Author(s) : Gould, Michael N. ; Ariazi, Eric A.
Report Date : OCT 1996
Pagination or Media Count : 53
Abstract : Monoterpene-induced/repressed genes were identified in regressing rat mammary carcinomas treated with dietary limonene using a newly developed method termed subtractive display. The subtractive display screen identified 42 monoterpene-induced genes comprising 9 known genes and 33 unidentified genes, as well as 58 monoterpene-repressed genes comprising 1 known gene and 57 unidentified genes. Several of the identified differentially expressed genes are involved in the mitoinhibitory transforming growth factor B signal tranduction pathway, as demonstrated by isolation of the mannose 6-phosphateAnsulin-like growth factor II receptor and the transforming growth factor B type II receptor. The monoterpene induced/repressed genes indicate that apoptosis and differentiation act in concert to effect carcinoma regression. Apoptosis is suggested by the cloning of a marker of programmed cell death, lipocortin 1. Consistent with a differentiation/remodeling process occurring during tumor regression, subtractive display identified YWK-II and neuroligin 1. Thus far, of the cDNAs putatively identified as differentially expressed in this complex in situ carcinoma model, 5 were tested, and each one has been confirmed to be differentially expressed. Additionally, many of the identified known genes are expressed as rare transcripts and exhibit small but significant changes in abundance.
Descriptors : *GENES , *CANCER , *MAMMARY GLANDS , *BREAST CANCER , COMPUTER PROGRAMMING , NEOPLASMS , REGRESSION ANALYSIS , CLONES , GENETIC ENGINEERING , DEATH , CELLS(BIOLOGY) , SCREENS(DISPLAYS).
Subject Categories : ANATOMY AND PHYSIOLOGY
MEDICINE AND MEDICAL RESEARCH
Distribution Statement : APPROVED FOR PUBLIC RELEASE