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PMID: 9619830 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Prognostic significance of allelic losses in primary melanoma.

Oncogene ·Vol. 16 ·No. 17 ·1998-04-30 ·Pages 2213-8

Healy E, Belgaid C, Takata M, Harrison D, Zhu NW, Burd DA, Rigby HS, Matthews JN, Rees JL

Abstract

Loss of genetic material, including loss of loci on chromosome arms 6q, 9p, and 10q, occurs frequently in cutaneous melanoma but infrequently in benign melanocytic nevi or other melanocytic lesions, suggesting that these genetic alterations are important in the development and progression of melanoma. To examine whether allelic loss is of prognostic importance in melanoma, disease-free survival was related to loss of heterozygosity on 6q, 9p and 10q in 83 individuals with sporadic primary cutaneous melanoma. Loss of chromosome arms 6q and 10q were each significantly associated with a poorer clinical outcome (P=0.013 and P=0.001 respectively). In a subgroup of 41 subjects whose primary tumours were allelotyped, the fractional allelic loss (FAL) at 39 autosomal arms also significantly correlated with disease-free survival (P=0.013), with an increase in FAL associated with a poorer outcome; this association remained significant when controlled for tumour thickness (P=0.035). In addition, a greater proportion of cells were immunopositive for Ki67 antigen, p53 and p21WAF1 protein in the primary melanomas than in the benign melanocytic nevi, however, only p53 over-expression was significantly associated with improved survival (P=0.041).

MeSH Terms
Alleles Biomarkers, Tumor/biosynthesis Chromosome Deletion Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 9 Cyclin-Dependent Kinase Inhibitor p21 Cyclins/biosynthesis Disease-Free Survival Humans Ki-67 Antigen/biosynthesis Loss of Heterozygosity Melanoma/genetics,metabolism Prognosis Risk Assessment Skin Neoplasms/genetics,metabolism Tumor Suppressor Protein p53/biosynthesis
Chemicals
Biomarkers, Tumor CDKN1A protein, human Cyclin-Dependent Kinase Inhibitor p21 Cyclins Ki-67 Antigen Tumor Suppressor Protein p53
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Healy E
Department of Dermatology, University of Newcastle upon Tyne, UK.
Belgaid C
Takata M
Harrison D
Zhu N W
Burd D A
Rigby H S
Matthews J N
Rees J L
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1998-04-30
Pages
2213-8
Language
English
Region
England
NLM ID
8711562
Subset
IM
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