Loss of constitutional heterozygosity as determined through the analysis of restriction-fragment-length polymorphism (RFLP) on tumoral and constitutional DNA has proven to be helpful to delimit the location of tumor-suppressor genes in the human genome. In malignant gliomas this approach indicates t
Loss of heterozygosity for 10q loci in human gliomas
β Scribed by B. K. Ahmed Rasheed; Gregory N. Fuller; Allan H. Friedman; Darell D. Bigner; Dr. Sandra H. Bigner
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 730 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1045-2257
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β¦ Synopsis
Cytogenetic and RFLP studies have shown that chromosome I0 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 I I 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 I I tumors was located in IOq24-q26 between the markers pHUK-8 and pMCTI22.2. Genes Chrom Cancer 5:75-82 (1992). @ 1992 Wiley-Liss, Inc.
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