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Published in: European Journal of Medical Research 10/2010

01-12-2010 | Research

GNAS1 T393C polymorphism and disease progression in patients with malignant melanoma

Authors: UH Frey, A Fritz, S Rotterdam, KW Schmid, A Potthoff, P Altmeyer, W Siffert, NH Brockmeyer

Published in: European Journal of Medical Research | Issue 10/2010

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Abstract

Background

Once metastasized, despite a variety of therapeutic options, the prognosis of patients with malignant melanoma (MM) is still poor. Therefore, the search for reliable markers to identify patients with high risk of disease progression is of high clinical importance. We have recently shown that TT genotypes of the single-nucleotide polymorphism (SNP) T393C in the gene GNAS1 are significantly associated with better outcome in a variety of carcinomas.

Patients

In the present study we assessed whether the T393C SNP is also related to the clinical course in MM. 328 patients with MM were retrospectively genotyped and genotypes were correlated with clinical outcome.

Results

While the allele frequency in the MM group (fC 0.52) did not significantly differ from that of healthy blood donors, the T393C SNP was associated with tumor progression of MM. Carriers of the C-allele showed a significantly more severe tumor progression as estimated from the time period to develop metastasis (HR 2.2, 95% CI 1.1-3.2, p = 0.017). Proportions of 5-year metastasis-free intervals were 87.1% for TT genotypes and 66.0% for C-allele carriers. Moreover, multivariable Cox regression analysis including tumor stage and melanoma subtype proved the T393C polymorphism to be an independent factor for metastasis (p = 0.012).

Conclusions

In summary, the GNAS1 T393C SNP represents a genetic host factor for predicting tumor progression also in patients with MM; genotyping of this SNP may contribute to better define patients who could benefit from an early individualized therapy.
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Metadata
Title
GNAS1 T393C polymorphism and disease progression in patients with malignant melanoma
Authors
UH Frey
A Fritz
S Rotterdam
KW Schmid
A Potthoff
P Altmeyer
W Siffert
NH Brockmeyer
Publication date
01-12-2010
Publisher
BioMed Central
Published in
European Journal of Medical Research / Issue 10/2010
Electronic ISSN: 2047-783X
DOI
https://doi.org/10.1186/2047-783X-15-10-422

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