Medical University of Vienna
Department of Dermatology
Währinger Gürtel 18-20, 1090 Wien
T: +43 (0)1 40400-0
M3 Study Group
Department of Dermatology
Medical University of Vienna
Währinger Gürtel 18-20
A-1090 Vienna, Austria
Group leader
Ichiro Okamoto
ichiro.okamoto@meduniwien.ac.at
Tel: +43-(0)1-40400-77000
Group members
Judith Wendt
judith.wendt@meduniwien.ac.at
Tel: +43-(0)1-40400-77000
Christoph Müller
christoph.mueller@meduniwien.ac.at
Tel: +43-(0)1-40400-77000
Research area
The M3-study (Molecular Marker in Melanoma) has been established in 2008 to study genetic and phenotypic markers of melanoma risk and progression of current patients. Patients’ recruitment including controls for studies identifying risk factors are ongoing. So far, more than 1800 melanoma patients and more than 1600 controls have participated to this study. Participants with familial melanoma background, multiple primary melanomas and young melanoma patients are of special interest. The following list represents the most recent scientific output by the group:
List of publications
- Wendt J., Rauscher S., Burgstaller-Muehlbacher S., Fae I., Fischer G., Pehamberger H., Okamoto I. (2016) Human Determinants and the Role of Melanocortin-1-Receptor Variants in Melanoma Risk Independent of UV Radiation Exposure, JAMA Dermatology
- Muller, C., Wendt, J., Rauscher, S., Burgstaller-Muehlbacher, S., Sunder-Plassmann, R., Scheurecker, C., Richtig, E., Fae, I., Fischer, G., Pehamberger, H. & Okamoto, I. (2016) Characterization of high risk melanoma patients in Austria, Br J Dermatol. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/26800492 British Journal of Dermatology: http://onlinelibrary.wiley.com/doi/10.1111/bjd.14407/abstract;jsessionid=771C5A573D1A454531727ADE3D75CB27.f03t02
- Burgstaller-Muehlbacher, S., Marko, M., Muller, C., Wendt, J., Pehamberger, H. & Okamoto, I. (2015) Novel CDKN2A mutations in Austrian melanoma patients, Melanoma Res. 25, 412-20. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/26225579 Melanoma Research: http://journals.lww.com/melanomaresearch/pages/articleviewer.aspx?year=2015&issue=10000&article=00006&type=abstract
- Wendt, J., Rauscher, S., Burgstaller-Muhlbacher, S., Roka, F., Fae, I., Fischer, G., Pehamberger, H. & Okamoto, I. (2014) Actinic damage on the back is significantly determined by MC1R variants and previous sun exposure compared with other body sites in a multivariate analysis, Br J Dermatol. 171, 622-30. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/24665948 British Journal of Dermatology: http://onlinelibrary.wiley.com/doi/10.1111/bjd.12994/abstract
- Davies, J. R., Jewell, R., Affleck, P., Anic, G. M., Randerson-Moor, J., Ozola, A., Egan, K. M., Elliott, F., Garcia-Casado, Z., Hansson, J., Harland, M., Hoiom, V., Jian, G., Jonsson, G., Kumar, R., Nagore, E., Wendt, J., Olsson, H., Park, J. Y., Patel, P., Pjanova, D., Puig, S., Schadendorf, D., Sivaramakrishna Rachakonda, P., Snowden, H., Stratigos, A. J., Bafaloukos, D., Ogbah, Z., Sucker, A., Van den Oord, J. J., Van Doorn, R., Walker, C., Okamoto, I., Wolter, P., Barrett, J. H., Timothy Bishop, D. & Newton-Bishop, J. (2014) Inherited variation in the PARP1 gene and survival from melanoma, Int J Cancer. 135, 1625-33. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/24535833 International Journal of Cancer: http://onlinelibrary.wiley.com/doi/10.1002/ijc.28796/abstract http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4106984/
- Davies, J. R., Field, S., Randerson-Moor, J., Harland, M., Kumar, R., Anic, G. M., Nagore, E., Hansson, J., Hoiom, V., Jonsson, G., Gruis, N. A., Park, J. Y., Guan, J., Sivaramakrishna Rachakonda, P., Wendt, J., Pjanova, D., Puig, S., Schadendorf, D., Okamoto, I., Olsson, H., Affleck, P., Garcia-Casado, Z., Puig-Butille, J. A., Stratigos, A. J., Kodela, E., Donina, S., Sucker, A., Hosen, I., Egan, K. M., Barrett, J. H., van Doorn, R., Bishop, D. T. & Newton-Bishop, J. (2014) An inherited variant in the gene coding for vitamin D-binding protein and survival from cutaneous melanoma: a BioGenoMEL study, Pigment Cell Melanoma Res. 27, 234-43. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/24219834 Pigment Cell & Melanoma Research: http://onlinelibrary.wiley.com/doi/10.1111/pcmr.12193/abstract http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065372/
- Tschandl, P., Berghoff, A. S., Preusser, M., Burgstaller-Muehlbacher, S., Pehamberger, H., Okamoto, I. & Kittler, H. (2013) NRAS and BRAF mutations in melanoma-associated nevi and uninvolved nevi, PLoS One. 8, e69639. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/23861977 PLOS ONE: http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0069639 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3704624/
- Iles, M. M., Law, M. H., Stacey, S. N., Han, J., Fang, S., Pfeiffer, R., Harland, M., Macgregor, S., Taylor, J. C., Aben, K. K., Akslen, L. A., Avril, M. F., Azizi, E., Bakker, B., Benediktsdottir, K. R., Bergman, W., Scarra, G. B., Brown, K. M., Calista, D., Chaudru, V., Fargnoli, M. C., Cust, A. E., Demenais, F., de Waal, A. C., Debniak, T., Elder, D. E., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E. M., Goldstein, A. M., Gruis, N. A., Hansson, J., Helsing, P., Hocevar, M., Hoiom, V., Hopper, J. L., Ingvar, C., Janssen, M., Jenkins, M. A., Kanetsky, P. A., Kiemeney, L. A., Lang, J., Lathrop, G. M., Leachman, S., Lee, J. E., Lubinski, J., Mackie, R. M., Mann, G. J., Martin, N. G., Mayordomo, J. I., Molven, A., Mulder, S., Nagore, E., Novakovic, S., Okamoto, I., Olafsson, J. H., Olsson, H., Pehamberger, H., Peris, K., Grasa, M. P., Planelles, D., Puig, S., Puig-Butille, J. A., Randerson-Moor, J., Requena, C., Rivoltini, L., Rodolfo, M., Santinami, M., Sigurgeirsson, B., Snowden, H., Song, F., Sulem, P., Thorisdottir, K., Tuominen, R., Van Belle, P., van der Stoep, N., van Rossum, M. M., Wei, Q., Wendt, J., Zelenika, D., Zhang, M., Landi, M. T., Thorleifsson, G., Bishop, D. T., Amos, C. I., Hayward, N. K., Stefansson, K., Bishop, J. A. & Barrett, J. H. (2013) A variant in FTO shows association with melanoma risk not due to BMI, Nat Genet. 45, 428-32. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/23455637 Nature genetics: http://www.nature.com/ng/journal/v45/n4/full/ng.2571.html http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640814/
- Davies, J. R., Field, S., Randerson-Moor, J., Harland, M., Kumar, R., Anic, G. M., Nagore, E., Hansson, J., Hoiom, V., Jonsson, G., Gruis, N. A., Park, J. Y., Jian, G., Rachakonda, P. S., Wendt, J., Pjanova, D., Puig, S., Schadendorf, D., Okamoto, I., Olsson, H., Affleck, P., Garcia-Casado, Z., Puig-Butille, J. A., Stratigos, A. J., Kodela, E., Donina, S., Sucker, A., Hosen, I., Egan, K. M., Barrett, J. H., van Doorn, R., Bishop, D. T. & Newton-Bishop, J. (2013) An inherited variant in the gene coding for vitamin D binding protein and survival from cutaneous melanoma: a BioGenoMEL study, Pigment Cell Melanoma Res. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/24219834 Pigment Cell & Melanoma Research: http://onlinelibrary.wiley.com/doi/10.1111/pcmr.12193/abstract http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065372/
- Wendt, J., Schanab, O., Binder, M., Pehamberger, H. & Okamoto, I. (2012) Site-dependent actinic skin damage as risk factor for melanoma in a central European population, Pigment Cell Melanoma Res. 25, 234-42. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/22145962 Pigment Cell & Melanoma Research: http://onlinelibrary.wiley.com/doi/10.1111/j.1755-148X.2011.00946.x/abstract
- Davies, J. R., Randerson-Moor, J., Kukalizch, K., Harland, M., Kumar, R., Madhusudan, S., Nagore, E., Hansson, J., Hoiom, V., Ghiorzo, P., Gruis, N. A., Kanetsky, P. A., Wendt, J., Pjanova, D., Puig, S., Saiag, P., Schadendorf, D., Soufir, N., Okamoto, I., Affleck, P., Garcia-Casado, Z., Ogbah, Z., Ozola, A., Queirolo, P., Sucker, A., Barrett, J. H., van Doorn, R., Bishop, D. T. & Newton-Bishop, J. (2012) Inherited variants in the MC1R gene and survival from cutaneous melanoma: a BioGenoMEL study, Pigment Cell Melanoma Res. 25, 384-394. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/22325793 Pigment Cell & Melanoma Research: http://onlinelibrary.wiley.com/doi/10.1111/j.1755-148X.2012.00982.x/abstract http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490389/
- Swoboda, A., Rasin-Streden, D., Schanab, O., Okamoto, I., Pehamberger, H., Petzelbauer, P. & Mikula, M. (2011) Identification of genetic disparity between primary and metastatic melanoma in human patients, Genes Chromosomes Cancer. 50, 680-8. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/21584902 Genes, Chromosomes & Cancer: http://onlinelibrary.wiley.com/doi/10.1002/gcc.20890/abstract
- Bauer, J., Buttner, P., Murali, R., Okamoto, I., Kolaitis, N. A., Landi, M. T., Scolyer, R. A. & Bastian, B. C. (2011) BRAF mutations in cutaneous melanoma are independently associated with age, anatomic site of the primary tumor, and the degree of solar elastosis at the primary tumor site, Pigment Cell Melanoma Res. 24, 345-51. Pubmed: http://www.ncbi.nlm.nih.gov pubmed/21324100 Pigment Cell & Melanoma Research: http://onlinelibrary.wiley.com/doi/10.1111/j.1755-148X.2011.00837.x/abstract http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107974/
- Broekaert, S. M., Roy, R., Okamoto, I., van den Oord, J., Bauer, J., Garbe, C., Barnhill, R. L., Busam, K. J., Cochran, A. J., Cook, M. G., Elder, D. E., McCarthy, S. W., Mihm, M. C., Schadendorf, D., Scolyer, R. A., Spatz, A. & Bastian, B. C. (2010) Genetic and morphologic features for melanoma classification, Pigment Cell Melanoma Res. 23, 763-70. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/20874733 Pigment Cell & Melanoma Research: http://onlinelibrary.wiley.com/doi/10.1111/j.1755-148X.2010.00778.x/abstract http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107973/
- Stacey, S. N., Sulem, P., Masson, G., Gudjonsson, S. A., Thorleifsson, G., Jakobsdottir, M., Sigurdsson, A., Gudbjartsson, D. F., Sigurgeirsson, B., Benediktsdottir, K. R., Thorisdottir, K., Ragnarsson, R., Scherer, D., Hemminki, K., Rudnai, P., Gurzau, E., Koppova, K., Botella-Estrada, R., Soriano, V., Juberias, P., Saez, B., Gilaberte, Y., Fuentelsaz, V., Corredera, C., Grasa, M., Hoiom, V., Lindblom, A., Bonenkamp, J. J., van Rossum, M. M., Aben, K. K., de Vries, E., Santinami, M., Di Mauro, M. G., Maurichi, A., Wendt, J., Hochleitner, P., Pehamberger, H., Gudmundsson, J., Magnusdottir, D. N., Gretarsdottir, S., Holm, H., Steinthorsdottir, V., Frigge, M. L., Blondal, T., Saemundsdottir, J., Bjarnason, H., Kristjansson, K., Bjornsdottir, G., Okamoto, I., Rivoltini, L., Rodolfo, M., Kiemeney, L. A., Hansson, J., Nagore, E., Mayordomo, J. I., Kumar, R., Karagas, M. R., Nelson, H. H., Gulcher, J. R., Rafnar, T., Thorsteinsdottir, U., Olafsson, J. H., Kong, A. & Stefansson, K. (2009) New common variants affecting susceptibility to basal cell carcinoma, Nat Genet. 41, 909-14. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/19578363 Nature genetics: http://www.nature.com/ng/journal/v41/n8/full/ng.412.html http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2973331/
- Roka, F., Mastan, P., Binder, M., Okamoto, I., Mittlboeck, M., Horvat, R., Pehamberger, H. & Diem, E. (2008) Prediction of non-sentinel node status and outcome in sentinel node-positive melanoma patients, Eur J Surg Oncol. 34, 82-8. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/17360144 European Journal of Surgical Oncology: http://www.sciencedirect.com/science/article/pii/S0748798307000480
- Okamoto, I., Roka, F., Krogler, J., Endler, G., Kaufmann, S., Tockner, S., Marsik, C., Jilma, B., Mannhalter, C., Wagner, O. & Pehamberger, H. (2006) The EGF A61G polymorphism is associated with disease-free period and survival in malignant melanoma, J Invest Dermatol. 126, 2242-6. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/16691190 Journal of Investigative Dermatology: http://www.sciencedirect.com/science/article/pii/S0022202X15326415
- Okamoto, I., Krogler, J., Endler, G., Kaufmann, S., Mustafa, S., Exner, M., Mannhalter, C., Wagner, O. & Pehamberger, H. (2006) A microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with risk for melanoma, Int J Cancer. 119, 1312-5. Pubmed: http://www.ncbi.nlm.nih.gov/pubmed/16596642 International Journal of Cancer: http://onlinelibrary.wiley.com/doi/10.1002/ijc.21937/abstract