TY - JOUR
T1 - Comprehensive allelotyping of human renal cell carcinomas using microsatellite DNA probes
AU - Thrash-Bingham, Catherine A.
AU - Greenberg, Richard E.
AU - Howard, Sharon
AU - Bruzel, Alan
AU - Bremer, Marilyn
AU - Goll, Alex
AU - Salazar, Hernando
AU - Freed, Jerome J.
AU - Tartof, Kenneth D.
PY - 1995/3/28
Y1 - 1995/3/28
N2 - The von Hippel-Lindau locus on chromosome 3p is a tumor suppressor gene known to be involved in nonpapillary renal cell carcinoma. A previous loss of heterozygosity (LOH) study aimed at determining the allelotype of kidney tumors has indicated that in addition to 3p, chromosome arms 5q, 6q, 10q, 11q, 17p, and 19p may also harbor tumor suppressor genes. However, cytogenetic studies reveal that chromosomes 3p, 6q, 8p, 9pq, and 14q most frequently undergo karyotypic changes in renal tumors. To resolve these differences, a collection of microsatellite DNA probes has been used to scan for LOH so that 90% of individual tumor genomes were rendered informative for allele loss. The assay is capable of detecting quantitative genomic alterations in tumor cells as well. We find that LOH is most frequent for chromosome arm 3p. However, in no tumor is 3p exclusively affected. LOH for 6q, 8p, 9pq, and 14q is also distinctly elevated for both nonpapillary as well as papillary tumors and suggest that many of the tumor suppressor loci involved may be common to the etiology of both forms of kidney cancer.
AB - The von Hippel-Lindau locus on chromosome 3p is a tumor suppressor gene known to be involved in nonpapillary renal cell carcinoma. A previous loss of heterozygosity (LOH) study aimed at determining the allelotype of kidney tumors has indicated that in addition to 3p, chromosome arms 5q, 6q, 10q, 11q, 17p, and 19p may also harbor tumor suppressor genes. However, cytogenetic studies reveal that chromosomes 3p, 6q, 8p, 9pq, and 14q most frequently undergo karyotypic changes in renal tumors. To resolve these differences, a collection of microsatellite DNA probes has been used to scan for LOH so that 90% of individual tumor genomes were rendered informative for allele loss. The assay is capable of detecting quantitative genomic alterations in tumor cells as well. We find that LOH is most frequent for chromosome arm 3p. However, in no tumor is 3p exclusively affected. LOH for 6q, 8p, 9pq, and 14q is also distinctly elevated for both nonpapillary as well as papillary tumors and suggest that many of the tumor suppressor loci involved may be common to the etiology of both forms of kidney cancer.
KW - Alleles
KW - Carcinoma, Papillary/genetics
KW - Carcinoma, Renal Cell/genetics
KW - Chromosome Deletion
KW - Chromosome Mapping
KW - Chromosomes, Human
KW - Chromosomes, Human, Pair 16
KW - Chromosomes, Human, Pair 3
KW - DNA Probes
KW - DNA, Neoplasm/isolation & purification
KW - DNA, Satellite/genetics
KW - Genes, Tumor Suppressor
KW - Genetic Markers
KW - Humans
KW - In Situ Hybridization, Fluorescence
KW - Kidney Neoplasms/genetics
KW - Lymphocytes
KW - Ploidies
KW - Polymerase Chain Reaction
KW - Polymorphism, Genetic
KW - von Hippel-Lindau Disease/genetics
UR - http://www.scopus.com/inward/record.url?scp=0028930201&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:A1995QP88900091&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1073/pnas.92.7.2854
DO - 10.1073/pnas.92.7.2854
M3 - Article
C2 - 7708737
SN - 0027-8424
VL - 92
SP - 2854
EP - 2858
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 7
ER -