MC1R variation and melanoma risk in the Swedish population in relation to clinical and pathological parameters
Författare
Summary, in English
The genetic background of cutaneous malignant melanoma (CMM) includes both germ line aberrations in high-penetrance genes, like CDKN2A, and allelic variation in low-penetrance genes like the melanocortin-1 receptor gene, MC1R. Red-hair colour associated MC1R alleles (RHC) have been associated with red hair, fair skin and risk of CMM. We investigated MC1R and CDKN2A variation in relation to phenotype, clinical factors and CMM risk in the Swedish population. The study cohort consisted of sporadic primary melanoma patients, familial melanoma patients and a control group. An allele-dose dependent increase in melanoma risk for carriers of variant MC1R alleles (after adjusting for phenotype), with an elevated risk among familial CMM patients, was observed. This elevated risk was found to be significantly associated with an increased frequency of dysplastic nevi (DN) among familial patients compared to sporadic patients. MC1R variation was found to be less frequent among acral lentiginous melanomas (ALM) and dependent on tumour localisation. No association was found between CDKN2A gene variants and general melanoma risk. Two new variants in the POMC gene were identified in red haired individuals without RHC alleles.
Avdelning/ar
- Chronic Inflammatory and Degenerative Diseases Research Unit
Publiceringsår
2009
Språk
Engelska
Sidor
196-204
Publikation/Tidskrift/Serie
Pigment Cell & Melanoma Research
Volym
22
Issue
2
Länkar
Dokumenttyp
Artikel i tidskrift
Förlag
Wiley-Blackwell
Ämne
- Cancer and Oncology
Nyckelord
- phenotype
- association
- melanoma
- MC1R
- dysplastic nevi
Status
Published
Forskningsgrupp
- Chronic Inflammatory and Degenerative Diseases Research Unit
ISBN/ISSN/Övrigt
- ISSN: 1755-148X