Whole genome amplification and high-throughput allelotyping identified five distinct deletion regions on chromosomes 5 and 6 in microdissected early-stage ovarian …

VW Wang, DA Bell, RS Berkowitz, SC Mok - Cancer research, 2001 - AACR
VW Wang, DA Bell, RS Berkowitz, SC Mok
Cancer research, 2001AACR
Investigation of genetic changes in tumors by loss of heterozygosity is a powerful technique
for identifying chromosomal regions that may contain tumor suppressor genes. In this study,
we determined allelic loss on chromosomes 5 and 6 in 29 primary early-stage epithelial
ovarian carcinomas including 3 microscopically identified adenocarcinomas using a high-
throughput PCR-based method combined with laser capture microdissection and whole
genome amplification techniques. Twenty microsatellite markers spanning chromosomes 5 …
Abstract
Investigation of genetic changes in tumors by loss of heterozygosity is a powerful technique for identifying chromosomal regions that may contain tumor suppressor genes. In this study, we determined allelic loss on chromosomes 5 and 6 in 29 primary early-stage epithelial ovarian carcinomas including 3 microscopically identified adenocarcinomas using a high-throughput PCR-based method combined with laser capture microdissection and whole genome amplification techniques. Twenty microsatellite markers spanning chromosomes 5 and 6 at an average distance of 20 cM were examined. High frequencies of loss on chromosome 5 were identified at loci D5S428 (48%), D5S424 (32%), and D5S630 (32%). Our study also showed that chromosome 6 exhibited high frequencies of loss of heterozygosity at loci D6S1574 (46%), D6S287 (42%), D6S441 (45%), D6S264 (60%), and D6S281 (35%). These results suggest that multiple tumor suppressor genes are located on five distinct regions on chromosomes 5 and 6, i.e., 5p15.2, 5q13–21, 6p24–25, 6q21–23, and 6q25.1–27, and may be involved in the early development of ovarian carcinomas.
AACR