Analysis of TNF alpha -238, -308, -857 and -1031 promotor polymorphisms in GEP-NET (CROSBI ID 508860)
Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija
Podaci o odgovornosti
Berković, Maja ; Čačev, Tamara ; Zjačić-Rotkvić Vanja ; Kapitanović ; Sanja
engleski
Analysis of TNF alpha -238, -308, -857 and -1031 promotor polymorphisms in GEP-NET
Neuroendocrine tumors of the gut and pancreas (GEP-NET) produce biogenic amines, peptides and chromogranins, especially chromogranine A (CgA). It has been shown that CgA levels correlate with TNF and soluble TNF receptors, suggesting a regulatory link with this inflammatory cytokine and its role in tumor growth and morphogenesis. TNF alpha gene is mapped to chromosome 6p21.3 and a large number of polymorphisms of its promoter have been described. The aim of our study was to estimate allelic frequency for four promoter SNPs in TNF alpha gene, -238, -308, -857 and -1031, in patients with GEP-NET. DNAs obtained from 30 GEP-NET patients and 150 unrelated healthy volunteers were genotyped for the TNF alpha -238, -308, -857 and -1031 SNPs using real-time PCR TaqMan® ; ; SNP genotyping assays. There was no statistically significant difference in the frequency of alleles associated with altered TNF alpha production between healthy population and patients with GEP-NET. The association between other TNF alpha promoter polymorphism and GEP-NET tumors has to be investigated in the future studies.
GEP-NET; TNF alpha polymorphism
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Podaci o prilogu
2005.
objavljeno
Podaci o matičnoj publikaciji
European Congress of endocrinology
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Gothenburg:
Podaci o skupu
European Congress of endocrinology
poster
03.09.2005-07.09.2005
Göteborg, Švedska