Volume 119, Issue 7 pp. 1736-1737
Short Report

ARLTS1 variants and melanoma risk

Bernd Frank

Corresponding Author

Bernd Frank

Division of Molecular Genetic Epidemiology, German Cancer Research Center, DKFZ, Heidelberg, Germany

Bernd Frank and Peter Meyer contributed equally to this work.

Fax: +49-6221-421810.

German Cancer Research Center (DKFZ), Division of Molecular Genetic Epidemiology, Im Neuenheimer Feld 580, 69120 Heidelberg, GermanySearch for more papers by this author
Peter Meyer

Peter Meyer

Dermatology Clinic, University Hospital of Tuebingen, Tuebingen, Germany

Institute of Human Genetics, Molecular Oncogenetics Unit, University Hospital of Tuebingen, Tuebingen, Germany

Genefinder Technologies Ltd., Munich, Germany

Bernd Frank and Peter Meyer contributed equally to this work.

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Melanie Barbara Boettger

Melanie Barbara Boettger

Dermatology Clinic, University Hospital of Tuebingen, Tuebingen, Germany

Genefinder Technologies Ltd., Munich, Germany

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Kari Hemminki

Kari Hemminki

Division of Molecular Genetic Epidemiology, German Cancer Research Center, DKFZ, Heidelberg, Germany

Department of Biosciences at Novum, Karolinska Institute, Huddinge, Sweden

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Henrike Stapelmann

Henrike Stapelmann

Institute of Human Genetics, Molecular Oncogenetics Unit, University Hospital of Tuebingen, Tuebingen, Germany

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Andreas Gast

Andreas Gast

Division of Molecular Genetic Epidemiology, German Cancer Research Center, DKFZ, Heidelberg, Germany

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Christina Schmitt

Christina Schmitt

Dermatology Clinic, University Hospital of Tuebingen, Tuebingen, Germany

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Rajiv Kumar

Rajiv Kumar

Division of Molecular Genetic Epidemiology, German Cancer Research Center, DKFZ, Heidelberg, Germany

Department of Biosciences at Novum, Karolinska Institute, Huddinge, Sweden

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Consolato Sergi

Consolato Sergi

Institute of Pathology, University Hospital, Innsbruck, Austria

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Barbara Burwinkel

Barbara Burwinkel

Division of Molecular Genetic Epidemiology, German Cancer Research Center, DKFZ, Heidelberg, Germany

Helmholtz-University Group Molecular Epidemiology, German Cancer Research Center, DKFZ, Heidelberg, Germany

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First published: 18 July 2006
Citations: 19

Fax: +49-6221-421810.

Abstract

Variants in the tumor suppressor gene ARLTS1 (ADP-ribosylation factor-like tumor-suppressor gene 1) have been shown to influence familial cancer risk. Both Cys148Arg and Trp149Stop were associated with an increased risk of familial or high-risk familial breast cancer, respectively. We studied the impact of these gene variants on melanoma risk, investigating 351 melanoma patients and 804 control subjects. While ARLTS1 Trp149Stop did not influence melanoma risk (OR = 0.83, 95% CI = 0.37–1.88, p = 0.65), Cys148Arg revealed a statistically significant association with an increased risk for heterozygous carriers (OR = 1.43, 95% CI = 1.05–1.95, p = 0.02). An additional risk enhancement, though statistically non-significant, was observed in individuals with multiple melanomas (OR = 2.33, 95% CI = 0.87–6.26, p = 0.08). © 2006 Wiley-Liss, Inc.

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