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PMID: 1384665 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Loss of heterozygosity for 10q loci in human gliomas.

Genes, chromosomes & cancer ·Vol. 5 ·No. 1 ·1992-07-00 ·Pages 75-82

Rasheed BK, Fuller GN, Friedman AH, Bigner DD, Bigner SH

Abstract

Cytogenetic and RFLP studies have shown that chromosome 10 is frequently lost in tumor cells from glioblastomas, suggesting that a suppressor gene important in tumorigenesis is present on this chromosome. Forty-one tumors were examined for loss of heterozygosity at 23 loci on chromosome 10 to determine the smallest common deletion interval on this chromosome. Seven tumors did not lose heterozygosity for any of the markers. Twenty-three tumors lost an allele for all the informative loci. In 11 tumors heterozygosity was maintained at some loci and lost at other loci, indicating partial deletion of chromosome 10. The common region of deletion in these 11 tumors was located in 10q24-q26 between the markers pHUK-8 and pMCT122.2.

Related Genes
MeSH Terms
Alleles Brain Neoplasms/genetics Chromosome Deletion Chromosomes, Human, Pair 10/ultrastructure DNA Probes Female Genetic Markers Glioblastoma/genetics Glioma/genetics Humans Male Polymorphism, Restriction Fragment Length
Chemicals
DNA Probes Genetic Markers
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Rasheed B K
Department of Pathology, Duke University Medical Center, Durham, North Carolina 27710.
Fuller G N
Friedman A H
Bigner D D
Bigner S H
Article Info
Journal
Genes, chromosomes & cancer
Abbr.
Genes Chromosomes Cancer
ISSN
1045-2257
Published
1992-07-00
Pages
75-82
Language
English
Region
United States
NLM ID
9007329
Subset
IM
Grants
NCI NIH HHS · CA 32672 · United States
NCI NIH HHS · CA 43722 · United States
NINDS NIH HHS · NS 20023 · United States
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