Artikel
Angiocentric gliomas are characterized by unmethylated MGMT-promoter and do not harbor BRAF or IDH1/2 mutations.
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Veröffentlicht: | 11. September 2012 |
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Gliederung
Text
Angiocentric glioma is a rare epilepsy-associated cerebrocortical tumor of uncertain relationship to other neuroepithelial tumors. Recently IDH1/2 mutations have emerged as a hallmark of diffuse astrocytomas and oligodendrogliomas and BRAF V600E point mutations are common in gangliogliomas and pleomorphic xanthoastrocytomas. The presence and putative role of these mutations in angiocentric glioma is still unclear.
We here analyzed a series of 12 resected angiocentric gliomas from 11 patients for mutations of IDH1/2 and BRAF by immunohistochemistry (H09 and VE1; 12/12 cases) and direct sequencing (8/12 cases). Additionally MGMT promoter methylation was assessed by methylation specific PCR and pyrosequencing in 8/12 cases.
All cases were negative for H09 (IDH1 R132H) and VE1 (BRAF V600E) immunohistochemistry. Consistent with this, sequencing of IDH1, IDH2 and BRAF revealed wild type status in all investigated cases. None of the investigated cases demonstrated a methylated MGMT promoter.
We conclude that IDH1/2 and BRAF mutations are not a common feature of angiocentric glioma. These genetic alterations may be useful for the differentiation of this rare epilepsy-associated tumor type from IDH1 mutated gliomas as well as from BRAF mutated gangliogliomas and pleomorphic xanthoastrocytomas. Furthermore, lack of MGMT promoter methylation might predict temozolomide as unpromising in cases not treatable by surgery or radiotherapy.