Molecular Subgroups of Medulloblastoma: an International Meta-Analysis of Transcriptome, Genetic Aberrations, and Clinical Data of WNT, SHH, Group 3, and Group 4 Medulloblastomas

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Molecular Subgroups of Medulloblastoma: an International Meta-Analysis of Transcriptome, Genetic Aberrations, and Clinical Data of WNT, SHH, Group 3, and Group 4 Medulloblastomas

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Title: Molecular Subgroups of Medulloblastoma: an International Meta-Analysis of Transcriptome, Genetic Aberrations, and Clinical Data of WNT, SHH, Group 3, and Group 4 Medulloblastomas
Author: Kool, Marcel; Korshunov, Andrey; Remke, Marc; Schlanstein, Maria; Northcott, Paul A.; Cho, Yoon-Jae; Koster, Jan; Schouten-van Meeteren, Antoinette; van Vuurden, Dannis; Clifford, Steven C.; Pietsch, Torsten; von Bueren, Andre O.; Rutkowski, Stefan; McCabe, Martin; Collins, V. Peter; Bäcklund, Magnus L.; Haberler, Christine; Bourdeaut, Franck; Delattre, Olivier; Doz, Francois; Ellison, David W.; Gilbertson, Richard J.; Lichter, Peter; Pfister, Stefan M.; Pomeroy, Scott L.; Taylor, Michael D.; Jones, David T. W.

Note: Order does not necessarily reflect citation order of authors.

Citation: Kool, Marcel, Andrey Korshunov, Marc Remke, David T. W. Jones, Maria Schlanstein, Paul A. Northcott, Yoon-Jae Cho, et al. 2012. Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas. Acta Neuropathologica 123(4): 473-484.
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Abstract: Medulloblastoma is the most common malignant brain tumor in childhood. Molecular studies from several groups around the world demonstrated that medulloblastoma is not one disease but comprises a collection of distinct molecular subgroups. However, all these studies reported on different numbers of subgroups. The current consensus is that there are only four core subgroups, which should be termed WNT, SHH, Group 3 and Group 4. Based on this, we performed a meta-analysis of all molecular and clinical data of 550 medulloblastomas brought together from seven independent studies. All cases were analyzed by gene expression profiling and for most cases SNP or array-CGH data were available. Data are presented for all medulloblastomas together and for each subgroup separately. For validation purposes, we compared the results of this meta-analysis with another large medulloblastoma cohort (n = 402) for which subgroup information was obtained by immunohistochemistry. Results from both cohorts are highly similar and show how distinct the molecular subtypes are with respect to their transcriptome, DNA copy-number aberrations, demographics, and survival. Results from these analyses will form the basis for prospective multi-center studies and will have an impact on how the different subgroups of medulloblastoma will be treated in the future.
Published Version: doi:10.1007/s00401-012-0958-8
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306778/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8735554

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