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Der Heme Oxygenase-1 GTn Promotor Polymorphismus ist ein Prädiktor für das rezidivfreie Überleben und das Gesamtüberleben bei duktalen Adenokarzinomen des Pankreas

Heme oxygenase-1 GTn promotor polymorphism is a prognosticator of tumor recurrence and survival in pancreatic cancer

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Chirurgisches Forum und DGAV Forum 2010

Abstract

Heme oxygenase-1 (HO-1) correlates with aggressive tumor behavior and chemotherapy resistance in pancreatic cancer (PC). We evaluated the prognostic value of the basal transcription controlling GTn repeat polymorphism (GTn) in the promoter region of the HO-1 gene in PC. Methods: We determined the GTn in 100 controls and 150 PAC patients. DNA was extracted from blood leucocytes and GTn determined by PCR, electrophoresis and sequencing. Clinicopathological parameters, disease- free and overall survival (DFS, OS) were correlated with GTn. Results: Three genotypes were defined based on short (S) < 25 and long (L) ≥ 25 GTn repeat alleles. In PC patients, a steadily increasing risk was evident between LL, SL and SS genotype patients for larger tumor size, presence of lymph node metastasis, poor tumor differentiation and higher recurrence rate (p < 0.001 each). The SS genotype displayed the most aggressive tumor biology. The LL genotype had the best and the SS genotype the worst DFS and OS (p < 0.001 each). The GTn genotype was the strongest prognostic factor for recurrence and survival (p < 0.001 each). Conclusion: The GTn repeat polymorphism is a strong prognostic marker for recurrence and survival in PC patients.

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Uzunoglu, G. et al. (2010). Der Heme Oxygenase-1 GTn Promotor Polymorphismus ist ein Prädiktor für das rezidivfreie Überleben und das Gesamtüberleben bei duktalen Adenokarzinomen des Pankreas. In: Gradinger, R., Menger, M., Meyer, HJ. (eds) Chirurgisches Forum und DGAV Forum 2010. Deutsche Gesellschaft für Chirurgie, vol 39. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-12192-0_38

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  • DOI: https://doi.org/10.1007/978-3-642-12192-0_38

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-12191-3

  • Online ISBN: 978-3-642-12192-0

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