Yuan Ping, Cao Jin-lin, Abuduwufuer Abudumailamu, Wang Lu-Ming, Yuan Xiao-Shuai, Lv Wang, Hu Jian
Department of Thoracic Surgery, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China, 310003.
PLoS One. 2016 Jan 22;11(1):e0146803. doi: 10.1371/journal.pone.0146803. eCollection 2016.
The prevalence of telomerase reverse transcriptase (TERT) promoter mutations (pTERTm) in non-small-cell lung cancer (NSCLC) have been investigated, but the results were inconsistent. In addition, several studies have analysed the role of pTERTm in the etiology of various types of cancers, however, the results also remain inconsistent.
The genomic DNA sequence of 103 NSCLC samples were analysed to investigate the frequency of pTERTm in these patients and to establish whether these mutations are associated with their clinical data. Furthermore, a meta-analysis based on previously published articles and our cohort study was performed to investigate the association of pTERTm with patient gender, age at diagnosis, metastasis status, tumour stage and cancer prognosis (5-year overall survival rate).
In the cohort study, 4 patients had C228T and 2 had C250T, with a total mutation frequency up to 5.8%. Significant difference of clinical data between pTERTm carriers and noncarriers was only found in age at diagnosis. In the meta-analysis, We found that pTERTm carriers in cancer patients are older than noncarriers (Mean difference (MD) = 5.24; 95% confidence interval [CI], 2.00 to 8.48), male patients were more likely to harbour pTERTm (odds Ratios (OR) = 1.38; 95% CI, 1.22 to 1.58), and that pTERTm had a significant association with distant metastasis (OR = 3.78; 95% CI, 2.45 to 5.82), a higher tumour grade in patients with glioma (WHO grade III, IV vs. I, II: OR, 2.41; 95% CI, 1.88 to 3.08) and a higher tumour stage in other types of cancer (III, IV vs. I, II: OR, 2.48; 95% CI, 1.48 to 4.15). pTERTm was also significantly associated with a greater risk of death (hazard ratio = 1.71; 95% CI, 1.41 to 2.08).
pTERTm are a moderately prevalent genetic event in NSCLC. The current meta-analysis indicates that pTERTm is associated with patient age, gender and distant metastasis. It may serves as an adverse prognostic factor in individuals with cancers.
已对非小细胞肺癌(NSCLC)中端粒酶逆转录酶(TERT)启动子突变(pTERTm)的发生率进行了研究,但结果并不一致。此外,多项研究分析了pTERTm在各类癌症病因中的作用,然而结果同样存在分歧。
对103例NSCLC样本的基因组DNA序列进行分析,以研究这些患者中pTERTm的频率,并确定这些突变是否与其临床数据相关。此外,基于先前发表的文章和我们的队列研究进行了一项荟萃分析,以研究pTERTm与患者性别、诊断时年龄、转移状态、肿瘤分期和癌症预后(5年总生存率)之间的关联。
在队列研究中,4例患者发生C228T突变,2例发生C250T突变,总突变频率高达5.8%。仅在诊断年龄方面发现pTERTm携带者与非携带者的临床数据存在显著差异。在荟萃分析中,我们发现癌症患者中的pTERTm携带者比非携带者年龄更大(平均差异(MD)=5.24;95%置信区间[CI],2.00至8.48),男性患者更有可能携带pTERTm(优势比(OR)=1.38;95%CI,1.22至1.58),并且pTERTm与远处转移显著相关(OR=3.78;95%CI,2.45至5.82),在胶质瘤患者中肿瘤分级更高(世界卫生组织III、IV级与I、II级:OR,2.41;95%CI,1.88至3.08),在其他类型癌症中肿瘤分期更高(III、IV级与I、II级:OR,2.48;95%CI,1.48至4.15)。pTERTm也与更高的死亡风险显著相关(风险比=1.71;95%CI,1.41至2.08)。
pTERTm在NSCLC中是一种中等发生率的基因事件。当前的荟萃分析表明,pTERTm与患者年龄、性别和远处转移相关。它可能是癌症患者的一个不良预后因素。