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高碳酸酐酶-9表达可识别少突胶质细胞瘤中1p/19q共缺失的一个亚组及良好预后。

High Carbonic Anhydrase-9 Expression Identifies a Subset of 1p/19q Co-Deletion and Favorable Prognosis in Oligodendroglioma.

作者信息

Sathornsumetee Sith, Cheunsuchon Pornsuk, Sangruchi Tumtip

机构信息

Division of Neurology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand; NANOTEC-Mahidol University Center of Excellence in Nanotechnology for Cancer Diagnosis and Treatment, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Department of Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

World Neurosurg. 2016 Jul;91:518-523.e1. doi: 10.1016/j.wneu.2016.02.069. Epub 2016 Mar 4.

Abstract

OBJECTIVE

To investigate the relationship between 3 hypoxic markers, carbonic anhydrase-9 (CA-9), hypoxia-inducible factor (HIF)-1α, and HIF-2α and the traditional genetic markers, deletions of chromosomes 1p and 19q and Isocitrate dehydrogenase 1 (IDH1) R132H mutation in oligodendrogliomas.

METHODS

Thirty-one oligodendrogliomas (27 World Health Organization Grade [WHO] II and 4 WHO Grade III) were processed into tissue microarray. Fluorescence in situ hybridization was exploited to detect chromosome deletion, whereas immunohistochemistry was performed to assess IDH1R132H mutation, CA-9, HIF-1α, and HIF-2α expression.

RESULTS

The frequencies of 1p/19q co-deletion and IDH1 R132H mutation were 68% and 71%, respectively. High expression of CA-9 was observed in 42% and was associated with longer survival (P = 0.04) in WHO Grade II oligodendroglioma. High CA-9 expression also identified 62% of 1p/19q-codeleted oligodendroglioma (P = 0.001). In addition, all tumors with high CA-9 expression displayed 1p/19q-codeletion. HIF-1α and HIF-2α provided no additional prognostic value for survival.

CONCLUSIONS

High expression of CA-9, a marker for hypoxia and acidosis, is associated with favorable prognosis in oligodendroglioma. In addition, it may serve as a simple screening test for 1p/19q co-deletion if validated in larger cohorts.

摘要

目的

研究3种缺氧标志物碳酸酐酶-9(CA-9)、缺氧诱导因子(HIF)-1α和HIF-2α与少突胶质细胞瘤中传统遗传标志物1号染色体短臂(1p)和19号染色体长臂(19q)缺失及异柠檬酸脱氢酶1(IDH1)R132H突变之间的关系。

方法

将31例少突胶质细胞瘤(27例世界卫生组织[WHO]二级和4例WHO三级)制成组织芯片。采用荧光原位杂交检测染色体缺失,同时进行免疫组织化学检测以评估IDH1R132H突变、CA-9、HIF-1α和HIF-2α的表达。

结果

1p/19q联合缺失和IDH1 R132H突变的频率分别为68%和71%。42%的病例中观察到CA-9高表达,且在WHO二级少突胶质细胞瘤中与较长生存期相关(P = 0.04)。CA-9高表达还可识别出62%的1p/19q联合缺失的少突胶质细胞瘤(P = 0.001)。此外,所有CA-9高表达的肿瘤均显示1p/19q联合缺失。HIF-1α和HIF-2α对生存期无额外的预后价值。

结论

CA-9作为缺氧和酸中毒的标志物,其高表达与少突胶质细胞瘤的良好预后相关。此外,如果在更大队列中得到验证,它可能作为1p/19q联合缺失的一种简单筛查检测方法。

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