Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions. 1993

R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
Department of Human Genetics, University of Leiden, Medical Faculty, The Netherlands.

Loss of heterozygosity (LOH) of markers for chromosome 17 is the most frequent genetic change observed in breast cancer to date. To assess whether the location of several candidate target genes is compatible with patterns of allele losses in the individual tumors, we examined the LOH status of chromosome 17 in 109 primary breast tumors with 15 polymorphic DNA markers (three for 17p and 12 for 17q). Allelic imbalance (AI) at 17q was observed in 44 of the 97 informative cases. A significant correlation was found between AI at the long arm and AI at the short arm of chromosome 17. The patterns of AI on 17q in the tumors differed and were highly complex in some cases. A number of tumors showed AI distal to the growth hormone locus, whereas others showed AI exclusively proximal of this marker. These results indicate that there are at least two different regions of allele loss on 17q.

UI MeSH Term Description Entries
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D001943 Breast Neoplasms Tumors or cancer of the human BREAST. Breast Cancer,Breast Tumors,Cancer of Breast,Breast Carcinoma,Cancer of the Breast,Human Mammary Carcinoma,Malignant Neoplasm of Breast,Malignant Tumor of Breast,Mammary Cancer,Mammary Carcinoma, Human,Mammary Neoplasm, Human,Mammary Neoplasms, Human,Neoplasms, Breast,Tumors, Breast,Breast Carcinomas,Breast Malignant Neoplasm,Breast Malignant Neoplasms,Breast Malignant Tumor,Breast Malignant Tumors,Breast Neoplasm,Breast Tumor,Cancer, Breast,Cancer, Mammary,Cancers, Mammary,Carcinoma, Breast,Carcinoma, Human Mammary,Carcinomas, Breast,Carcinomas, Human Mammary,Human Mammary Carcinomas,Human Mammary Neoplasm,Human Mammary Neoplasms,Mammary Cancers,Mammary Carcinomas, Human,Neoplasm, Breast,Neoplasm, Human Mammary,Neoplasms, Human Mammary,Tumor, Breast
D002872 Chromosome Deletion Actual loss of portion of a chromosome. Monosomy, Partial,Partial Monosomy,Deletion, Chromosome,Deletions, Chromosome,Monosomies, Partial,Partial Monosomies
D002874 Chromosome Mapping Any method used for determining the location of and relative distances between genes on a chromosome. Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage
D002886 Chromosomes, Human, Pair 17 A specific pair of GROUP E CHROMOSOMES of the human chromosome classification. Chromosome 17
D005260 Female Females
D005819 Genetic Markers A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event. Chromosome Markers,DNA Markers,Markers, DNA,Markers, Genetic,Genetic Marker,Marker, Genetic,Chromosome Marker,DNA Marker,Marker, Chromosome,Marker, DNA,Markers, Chromosome
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000483 Alleles Variant forms of the same gene, occupying the same locus on homologous CHROMOSOMES, and governing the variants in production of the same gene product. Allelomorphs,Allele,Allelomorph
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA

Related Publications

R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
August 1991, Lancet (London, England),
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
May 1994, Genes, chromosomes & cancer,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
September 1993, Human genetics,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
May 2001, Cancer genetics and cytogenetics,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
December 1993, Cancer research,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
May 2000, Mutation research,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
October 2002, International journal of oncology,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
January 1994, International journal of cancer,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
February 1994, Genes, chromosomes & cancer,
R S Cornelis, and P Devilee, and M van Vliet, and N Kuipers-Dijkshoorn, and A Kersenmaeker, and A Bardoel, and P M Khan, and C J Cornelisse
May 1998, International journal of cancer,
Copied contents to your clipboard!