CRICM, Pierre and Marie Curie University, Paris, France; INSERM U 975, Paris, France; UMR 7225, CNRS, Paris, France.
Cancer. 2013 Feb 15;119(4):806-13. doi: 10.1002/cncr.27798. Epub 2012 Nov 26.
The IDH1 gene, which encodes isocitrate dehydrogenase 1, is frequently mutated in gliomas and acute myeloid leukemia. The single-nucleotide polymorphism (SNP) (reference SNP no. rs11554137:C>T) located on IDH1 codon 105 has been associated with a poor outcome in patients with acute myeloid leukemia but has not been investigated in patients with gliomas.
The IDH1 codon 105 SNP was genotyped first in a series of 952 patients with grade 2 through 4 gliomas and was correlated with outcomes and tumor genomic profile. Then, it was genotyped in 2 validations sets of 306 patients with glioblastoma (GBM) and 591 patients with glioma.
The minor allele codon 105 glycine (GGT) SNP (IDH1(105GGT) ) was identified in 98 of 952 patients (10.3%) and was not associated with the codon 132 (IDH1(132) ) mutation. Patients who had GMB with the IDH1(105GGT) variant had a poorer outcome than patients without the variant (median overall survival [OS], 10.7 months vs 15.5 months; P = .001; median progression-free survival [PFS], 6.4 months vs 8.5 months; P = .003). The prognostic impact was confirmed in an independent validation set of 306 GBMs from the same center (median PFS, 6.8 months vs 9.7 months; P = .006; median OS, 13.9 months vs 18.8 months; P = .0187). In the second validation cohort (591 grade 2-4 gliomas), a significant association was observed between IDH1(105GGT) and an adverse prognosis for the overall series and for patients with World Health Organization grade 3 gliomas, but the difference did not reach significance in patients with GBM.
Taken together, the current data strongly suggested an association between the SNP rs11554137:C>T polymorphism and adverse outcomes in patients with malignant glioma. A single-nucleotide polymorphism (SNP) located on codon 105 of the isocitrate dehydrogenase 1 (IDH1) gene (reference SNP rs11554137) is analyzed in 3 independent series of patients with gliomas. The SNP rs11554137 is independent of the occurrence of somatic mutation on IDH1 codon 132, but, per se, has a prognostic impact in malignant gliomas.
IDH1 基因编码异柠檬酸脱氢酶 1,在胶质瘤和急性髓系白血病中经常发生突变。位于 IDH1 密码子 105 的单核苷酸多态性(SNP)(参考 SNP 编号 rs11554137:C>T)与急性髓系白血病患者的不良预后相关,但尚未在胶质瘤患者中进行研究。
首先在 952 名 2 级至 4 级胶质瘤患者的一系列患者中对 IDH1 密码子 105SNP 进行了基因分型,并将其与结局和肿瘤基因组图谱进行了相关性分析。然后,在 306 名胶质母细胞瘤(GBM)患者和 591 名胶质瘤患者的 2 个验证集中进行了基因分型。
在 952 名患者中有 98 名(10.3%)发现了 IDH1 密码子 105 甘氨酸(GGT)SNP(IDH1(105GGT)),并且与 IDH1 密码子 132(IDH1(132))突变无关。携带 IDH1(105GGT)变异的 GBM 患者的预后比没有变异的患者差(中位总生存期[OS],10.7 个月 vs 15.5 个月;P =.001;中位无进展生存期[PFS],6.4 个月 vs 8.5 个月;P =.003)。该预后影响在来自同一中心的 306 例 GBM 的独立验证集中得到了证实(中位 PFS,6.8 个月 vs 9.7 个月;P =.006;中位 OS,13.9 个月 vs 18.8 个月;P =.0187)。在第二个验证队列(591 例 2-4 级胶质瘤)中,IDH1(105GGT)与总体系列和 3 级世界卫生组织胶质瘤患者的不良预后之间存在显著关联,但在 GBM 患者中差异未达到显著水平。
综上所述,目前的数据强烈表明,单核苷酸多态性 rs11554137:C>T 与恶性胶质瘤患者的不良预后之间存在关联。对 3 个独立系列的胶质瘤患者进行了 IDH1 基因(参考 SNP rs11554137)密码子 105 上的单核苷酸多态性(SNP)分析。SNP rs11554137 与 IDH1 密码子 132 上体细胞突变的发生无关,但本身在恶性胶质瘤中有预后影响。