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p73/p21 基因甲基化模式的频率变化与南印度人群不同级别胶质瘤之间的染色体畸变相关。

Frequency variations in the methylated pattern of p73/p21 genes and chromosomal aberrations correlating with different grades of glioma among south Indian population.

机构信息

Department of Biochemistry, University of Madras, Guindy Campus, Chennai, 25 Tamilnadu, India.

出版信息

Med Oncol. 2011 Dec;28 Suppl 1:S445-52. doi: 10.1007/s12032-010-9671-4. Epub 2010 Sep 16.

Abstract

Gliomas are the most common primary brain tumors in India. The main epigenetic modification in glioma is aberrant DNA methylation that is now renowned to be a common hallmark of brain tumors. This study was designed to determine the frequency of aberrant CpG island methylation in the promoter regions of p21 and p73 in different grades of glioma and to explore their respective chromosomal aberrations. Total of 160 patients with histologically confirmed grades of glioma (I, II, III, and IV) were included in the study. DNA samples from blood and brain tissues, including benign lesions were subjected to sodium bisulfite conversion and hypermethylation detection using methylation-specific PCR followed by RT-PCR. Western blotting was also carried out for p21 and its related protein, p53. A total of 124 of 160 glioma samples (77.5%) displayed CpG island hypermethylation of both p73, p21 genes associated with the loss of mRNA expression (P < 0.001) and the loss of protein expressions (p53 independent p21 expression). p73 gene showed increased methylation frequency in all grades, 40 of 60 (66%) glioblastomas and 16 of 30 (53.3%) anaplastic astrocytoma, 10 of 20(50%) oligodendrogliomas, 8 of 20 (40%) ependymoma, and low-grade glioma 6 of 20 (30%). The percentage of methylation significantly well correlated with the overall survival and also with chromosomal loss. Thus, the studied glioma patients among south Indians showed a high frequency of aberrant methylation with varied chromosomal signatures in different grades, playing a role in aggressiveness and characterization of a particular grade, the appreciation of which might help for designing a specific therapy.

摘要

神经胶质瘤是印度最常见的原发性脑肿瘤。神经胶质瘤的主要表观遗传修饰是异常的 DNA 甲基化,现在被认为是脑肿瘤的共同标志。本研究旨在确定不同级别神经胶质瘤中 p21 和 p73 启动子区异常 CpG 岛甲基化的频率,并探讨它们各自的染色体异常。本研究共纳入 160 例经组织学证实的神经胶质瘤(I、II、III 和 IV 级)患者。对包括良性病变在内的血液和脑组织的 DNA 样本进行亚硫酸氢盐转换和甲基化特异性 PCR 检测,然后进行 RT-PCR。还进行了 p21 及其相关蛋白 p53 的 Western 印迹分析。在 160 例神经胶质瘤样本中,共有 124 例(77.5%)显示 p73 和 p21 基因的 CpG 岛过度甲基化,与 mRNA 表达丧失(P < 0.001)和蛋白表达丧失(p53 独立的 p21 表达)有关。p73 基因在所有级别中均显示出较高的甲基化频率,60 例胶质母细胞瘤中有 40 例(66%),30 例间变性星形细胞瘤中有 16 例(53.3%),20 例少突胶质细胞瘤中有 10 例(50%),20 例室管膜瘤中有 8 例(40%),低级别胶质瘤中有 6 例(30%)。甲基化的百分比与总生存率显著相关,也与染色体缺失相关。因此,研究中的南亚神经胶质瘤患者表现出异常甲基化的高频率,不同级别具有不同的染色体特征,在侵袭性和特定级别特征方面发挥作用,对其的认识可能有助于设计特定的治疗方法。

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