A defined region of loss of heterozygosity at 11q23 in cutaneous malignant melanoma.
case_series · Level IV
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Abstract
Karyotypic and molecular data indicate that genetic alterations of the long arm of chromosome 11 (11q) may be involved in malignant melanoma. To test this we analyzed 5 polymorphic microsatellite repeats on 11q using a PCR-based assay for loss of heterozygosity in normal and tumor tissues from 24 individuals with cutaneous malignant melanoma of various stages. Our findings indicate that a tumor suppressor gene that plays a role in malignant melanoma is located on the long arm of chromosome 11, likely within a 51 cM region at 11q23. Its loss appears to be a late event in tumor progression and may serve as an indicator for a less favorable clinical outcome.
Medical subject headings
- Chromosome Deletion
- Chromosomes, Human, Pair 11
- Melanoma
- Skin Neoplasms