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PMID: 3342039 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Chromosome 5 allele loss at the glucocorticoid receptor locus in human colorectal carcinomas.

Biochemical and biophysical research communications ·Vol. 150 ·No. 2 ·1988-01-29 ·Pages 591-8

Wildrick DM, Boman BM

Abstract

Matched normal/tumor DNA pairs from sporadic colon carcinoma patients were examined for chromosome 5 allele loss using a probe for a functional gene (glucocorticoid receptor = GRL) locus. This locus maps (5q11-q13) close to one of two alternative sites recently reported for a constitutional deletion in a familial adenomatous polyposis (FAP) patient. Tumor-specific allele loss of at least 27% at GRL supports the hypothesis that both hereditary and sporadic forms of colon cancer result from mutations of the same gene. The proximity of the GRL locus to the region of 5q affected in FAP and the observed tumor-specific allele loss at this locus suggest that further research is needed regarding whether genetic alterations in the glucocorticoid receptor may be associated with colon carcinogenesis.

MeSH Terms
Adenocarcinoma/genetics,metabolism Alleles Chromosome Deletion Chromosomes, Human, Pair 5 Colonic Neoplasms/genetics,metabolism DNA, Neoplasm/genetics Humans Nucleic Acid Hybridization Receptors, Glucocorticoid/genetics Rectal Neoplasms/genetics,metabolism
Chemicals
DNA, Neoplasm Receptors, Glucocorticoid
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wildrick D M
University of Texas M. D. Anderson Hospital and Tumor Institute at Houston, Section of Gastrointestinal Oncology and Digestive Diseases 77030.
Boman B M
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1988-01-29
Pages
591-8
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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