Jeong Da Eun, Woo Seon Rang, Nam Hyun, Nam Do-Hyun, Lee Jae-Ho, Joo Kyeung Min
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.
Oncol Lett. 2017 Dec;14(6):8213-8219. doi: 10.3892/ol.2017.7196. Epub 2017 Oct 16.
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.
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。