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多形性胶质母细胞瘤启动子突变的临床前及临床意义

Preclinical and clinical implications of promoter mutation in glioblastoma multiforme.

作者信息

Jeong Da Eun, Woo Seon Rang, Nam Hyun, Nam Do-Hyun, Lee Jae-Ho, Joo Kyeung Min

机构信息

Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul 06531, Republic of Korea.

Department of Anatomy and Cell Biology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 06531, Republic of Korea.

出版信息

Oncol Lett. 2017 Dec;14(6):8213-8219. doi: 10.3892/ol.2017.7196. Epub 2017 Oct 16.

DOI:10.3892/ol.2017.7196
PMID:29344264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5755188/
Abstract

The promoter region of the telomerase reverse transcriptase gene () is mutated in a subpopulation of patients with glioblastoma multiforme (GBM). In the present study, preclinical and clinical implications of the mutation were analyzed in 25 GBMs to evaluate its utility as a therapeutic target. Associations between the promoter mutation and a number of preclinical/clinical characteristics were analyzed. Notably, the promoter mutation was identified in 92.3% of GBMs where dissociated cells revealed sphere formation capacity; while the promoter mutation was identified in 33.3% of GBMs without sphere formation capacity (P=0.004). In addition, this significantly increased mutation rate was observed in GBMs with tumorigenic potential (80% vs. 0%; P=0.004). Furthermore, patients with GBM exhibiting the promoter mutation demonstrated significantly decreased overall survival rate compared with patients lacking this mutation (81.7 vs. 152.6 weeks; P=0.026). The results of the present study indicated that the promoter mutation is associated with the self-renewal capacity of GBM cells and clinical aggressiveness of GBMs, which may be translated to a targeting therapy against TERT to inhibit the self-renewal of GBM cells.

摘要

端粒酶逆转录酶基因()的启动子区域在多形性胶质母细胞瘤(GBM)患者的一个亚群中发生突变。在本研究中,对25例GBM患者分析了该突变的临床前和临床意义,以评估其作为治疗靶点的效用。分析了启动子突变与一些临床前/临床特征之间的关联。值得注意的是,在92.3%的解离细胞具有成球能力的GBM中发现了启动子突变;而在33.3%的无成球能力的GBM中发现了启动子突变(P = 0.004)。此外,在具有致瘤潜能的GBM中观察到该突变率显著增加(80%对0%;P = 0.004)。此外,与缺乏该突变的患者相比,表现出启动子突变的GBM患者的总生存率显著降低(81.7对152.6周;P = 0.026)。本研究结果表明,启动子突变与GBM细胞的自我更新能力和GBM的临床侵袭性相关,这可能转化为针对TERT的靶向治疗以抑制GBM细胞的自我更新。

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本文引用的文献

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Targeting self-renewal pathways in cancer stem cells: clinical implications for cancer therapy.靶向癌症干细胞中的自我更新途径:对癌症治疗的临床意义。
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TERT promoter mutations and polymorphisms as prognostic factors in primary glioblastoma.端粒酶逆转录酶(TERT)启动子突变和多态性作为原发性胶质母细胞瘤的预后因素
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Prognostic quality of activating TERT promoter mutations in glioblastoma: interaction with the rs2853669 polymorphism and patient age at diagnosis.胶质母细胞瘤中TERT启动子激活突变的预后质量:与rs2853669多态性及诊断时患者年龄的相互作用
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Patient-derived xenografts from non-small cell lung cancer brain metastases are valuable translational platforms for the development of personalized targeted therapy.来源于非小细胞肺癌脑转移的患者源性异种移植物是开发个体化靶向治疗的有价值的转化平台。
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TERT promoter mutation designates biologically aggressive primary glioblastoma.端粒酶逆转录酶(TERT)启动子突变表明原发性胶质母细胞瘤具有生物学侵袭性。
Neuro Oncol. 2015 Jan;17(1):5-6. doi: 10.1093/neuonc/nou318. Epub 2014 Dec 1.
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Combined analysis of TERT, EGFR, and IDH status defines distinct prognostic glioblastoma classes.TERT、EGFR和IDH状态的联合分析定义了不同预后的胶质母细胞瘤类别。
Neurology. 2014 Sep 23;83(13):1200-6. doi: 10.1212/WNL.0000000000000814. Epub 2014 Aug 22.
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TERT promoter mutations: a novel independent prognostic factor in primary glioblastomas.端粒酶逆转录酶(TERT)启动子突变:原发性胶质母细胞瘤中一种新的独立预后因素。
Neuro Oncol. 2015 Jan;17(1):45-52. doi: 10.1093/neuonc/nou158. Epub 2014 Aug 18.
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