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Isocitrate dehydrogenase 1R132H mutation in microglia/macrophages in gliomas: Indication of a significant role of microglia/macrophages in glial tumorigenesis

机译:小胶质瘤/小胶质细胞中的异柠檬酸脱氢酶1R132H突变:指示小胶质细胞/巨噬细胞在神经胶质瘤发生中的重要作用

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textabstractSomatic mutation of Isocitrate dehydrogenase 1 (IDH1) at the locus of R132 (IDH1R132H) occurs in > 70% of WHO grades II-III gliomas and secondary glioblastomas. To date it remains unknown whether the mutation is restricted to glial tumor cells. Microglial cells are the resident macrophages in the central nervous system. Tumor-infiltrating microglial cells/macrophages are major stromal cellular components of malignant gliomas and substantially contribute to the tumor mass. Differential identification of the IDH1 R132H mutant cellular components is of particular importance for understanding of the mutation-associated tumor biology. Here we discovered that a significant portion of CD68+, Iba1+, CX3CR1+ microglial cells/macrophages also harbor the IDH1R132H mutation. The findings provide novel insights for understanding the mutation-associated tumor biology relevant to clinical applications as a predictive and/or prognostic marker or therapeutic target.
机译:textabstract在R132(IDH1R132H)所在地的异柠檬酸脱氢酶1(IDH1)发生体细胞突变发生在> 70%的WHO II-III级神经胶质瘤和继发性胶质母细胞瘤中。迄今为止,尚不清楚该突变是否限于神经胶质瘤细胞。小胶质细胞是中枢神经系统中的常驻巨噬细胞。肿瘤浸润性小胶质细胞/巨噬细胞是恶性神经胶质瘤的主要基质细胞成分,并实质上有助于肿瘤块。 IDH1 R132H突变细胞成分的差异鉴定对于理解与突变相关的肿瘤生物学特别重要。在这里,我们发现CD68 +,Iba1 +,CX3CR1 +小胶质细胞/巨噬细胞的很大一部分也带有IDH1R132H突变。这些发现为理解与临床应用相关的与突变相关的肿瘤生物学作为预测和/或预后标志物或治疗靶标提供了新颖的见解。

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