首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >A four-protein expression prognostic signature predicts clinical outcome of lower-grade glioma
【24h】

A four-protein expression prognostic signature predicts clinical outcome of lower-grade glioma

机译:四蛋白表达预后签名预测较低级胶质瘤的临床结果

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

BackgroundGlioma is a wide category of brain tumor originates from glial cells. Lower-Grade Glioma (LGG) consists of World Health Organization (WHO) grade II and grade III gliomas. Since the LGGs can infiltrate into adjacent areas, the complete removal of tumor is difficult and it results in recurrence and malignant progression to high grade glioma. Our study uncovers robust survival indicators in LGG which can be checked by immunohistochemistry to predict the outcome of lower grade. In addition, it unravelled the novel therapeutic targets in order to improve the survival of LGG patients. MethodsTo identify a prognostic signature based on protein expression in LGGs, we analysed Reverse Phase Protein Array data of LGG samples (n?=?380) from The Cancer Genome Atlas cohort. We made random stratification of samples into discovery (n?=?228) and validation datasets (n?=?152). We performed multivariate Cox proportional hazards regression analysis of proteins (n?=?219) using discovery dataset with age, WHO grade and IDH mutation status. ResultsWe identified four-protein prognostic signature that can segregate patients into high- and low-risk. The signature estimates poor overall survival for high-risk patients in both discovery (hazard ratio [HR]?=?4.11; 95% confidence interval [CI]?=?2.18–7.75;p?
机译:背景凝血瘤是一种广泛的脑肿瘤,来自胶质细胞。较低级胶质瘤(LGG)由世界卫生组织(世卫组织)二级和III级胶质组织组成。由于LGGS可以渗入相邻区域,因此肿瘤的完全除去难落,并且导致高级胶质瘤的复发和恶性进展。我们的研究揭示了LGG中的强大生存指标,可以通过免疫组化来检查以预测较低等级的结果。此外,它揭开了新的治疗靶标,以改善LGG患者的存活。方法鉴定基于LGGS中的蛋白质表达的预后签名,我们分析了来自癌症基因组Atlas Cohort的LGG样品的反向蛋白阵列数据(n?= 380)。我们将样本的随机分层进行了发现(n?=?228)和验证数据集(n?=?152)。我们使用具有年龄的Discovery DataSet进行蛋白质(n?= 219)的多变量Cox比例危害的复发分析,WHO级别和IDH突变状态。结果鉴定了四蛋白质预后签名,可以将患者分成高风险和低风险。签名估计在发现的高风险患者(危险比[HR] = 4.11; 95%置信区间[CI]?=?2.18-7.75; p?<0.0001)和验证数据集(HR ?=?3.49; 95%CI?=?1.52-8.01; p?<0.0001)。在四个标记中,发现CHK2_PT68是保护性的,而MSH6,ARID1A和帕雪林与存活率不良有关。此外,随着年龄的年龄和IDH突变状态的这种签名的多变量Cox比例危害对该签名的回归分析显示,该预后签名是两个数据集中的独立预测者。结论您的发现发现了一组潜在的蛋白质生物标志物预测存活率,并有助于随后的LGG患者治疗管理。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号