Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas

Fontebasso, Adam M. and Schwartzentruber, Jeremy and Khuong-Quang, Dong-Anh and Liu, Xiao-Yang and Sturm, Dominik and Korshunov, Andrey and Jones, David T. W. and Witt, Hendrik and Kool, Marcel and Albrecht, Steffen and Fleming, Adam and Hadjadj, Djihad and Busche, Stephan and Lepage, Pierre and Montpetit, Alexandre and Staffa, Alfredo and Gerges, Noha and Zakrzewska, Magdalena and Zakrzewski, Krzystof and Liberski, Pawel P. and Hauser, Peter and Garami, Miklós and Klekner, Álmos and Bognár, László and Zadeh, Gelareh and Faury, Damien and M. Pfister, Stefan and Jabado, Nada and Majewski, Jacek (2013) Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas. Acta Neuropathologica, 125 (5). pp. 659-669. ISSN 0001-6322

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Recurrent mutations affecting the histone H3.3 residues Lys27 or indirectly Lys36 are frequent drivers of pediatric high-grade gliomas (over 30 % of HGGs). To identify additional driver mutations in HGGs, we investigated a cohort of 60 pediatric HGGs using whole-exome sequencing (WES) and compared them to 543 exomes from non-cancer control samples. We identified mutations in SETD2, a H3K36 trimethyltransferase, in 15 % of pediatric HGGs, a result that was genome-wide significant (FDR = 0.029). Most SETD2 alterations were truncating mutations. Sequencing the gene in this cohort and another validation cohort (123 gliomas from all ages and grades) showed SETD2 mutations to be specific to high-grade tumors affecting 15 % of pediatric HGGs (11/73) and 8 % of adult HGGs (5/65) while no SETD2 mutations were identified in low-grade diffuse gliomas (0/45). Furthermore, SETD2 mutations were mutually exclusive with H3F3A mutations in HGGs (P = 0.0492) while they partly overlapped with IDH1 mutations (4/14), and SETD2- mutant tumors were found exclusively in the cerebral hemispheres (P = 0.0055). SETD2 is the only H3K36 trimethyltransferase in humans, and SETD2-mutant tumors showed a substantial decrease in H3K36me3 levels (P\0.001), indicating that the mutations are loss-offunction. These data suggest that loss-of-function SETD2 mutations occur in older children and young adults and are specific to HGG of the cerebral cortex, similar to the H3.3 G34R/V and IDH mutations. Taken together, our results suggest that mutations disrupting the histone code at H3K36, including H3.3 G34R/V, IDH1 and/or SETD2 mutations, are central to the genesis of hemispheric HGGs in older children and young adults.

Item Type: Article
Uncontrolled Keywords: High-grade glioma, H3K36 methylation, SETD2, Epigenetic, Pediatric, Young adult
Subjects: R Medicine / orvostudomány > RC Internal medicine / belgyógyászat > RC0254 Neoplasms. Tumors. Oncology (including Cancer) / daganatok, tumorok, onkológia
Depositing User: Dr. Álmos Klekner
Date Deposited: 26 Sep 2014 17:52
Last Modified: 26 Sep 2014 17:52

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