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Basal cell carcinoma is associated with high TNF-alpha release but nor with TNF-alpha polymorphism at position--308

Lone Skov, Michael H Allen, Bo Bang, David Francis, Jonathan N W N Barker, Ole Baadsgaard

12 Citations (Scopus)

Abstract

The mechanisms underlying induction of UVB-induced immunosuppression are not fully understood, but tumor necrosis factor alpha (TNF-alpha) is suggested to play a central role. A single base pair polymorphism at position --308 in the promoter region of the TNF-alpha gene associated with an enhanced secretion of TNF-alpha has been identified in humans. We have therefore investigated the association of the --308 polymorphism with the risk of basal cell carcinoma (BCC) in humans. The frequency of TNF G and TNF A alleles among Caucasian patients with a previous BCC (n=191) and health adults (n-107) were compared. For the TNF--308 polymorphism there was significant association between the genotype or allele frequencies and having BCC. To determine whether patients with a previous BCC had an increased capacity to secrete TNF-alpha, mononuclear cells were stimulated with lipopolysaccharide. Mononuclear cells from patients with a previous BCC (n=15) demonstrated a significantly increased release of TNF-alpha upon stimulation with lipopolysaccharide (P<0.03) compared with mononuclear cells age-matched control subjects (n=16). Further studies of other polymorphisms of the TNF-alpha gene associated with increased TNF-alpha production and BCC and necessary.

Original languageEnglish
JournalExperimental Dermatology
Volume12
Issue number6
Pages (from-to)772-6
Number of pages5
ISSN0906-6705
Publication statusPublished - Dec 2003

Keywords

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Carcinoma, Basal Cell
  • Case-Control Studies
  • DNA
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Leukocytes, Mononuclear
  • Linkage Disequilibrium
  • Lipopolysaccharides
  • Male
  • Middle Aged
  • Polymorphism, Genetic
  • Risk Factors
  • Tumor Necrosis Factor-alpha

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