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Clinicopathological and prognostic significance of mTOR and phosphorylated mTOR expression in patients with esophageal squamous cell carcinoma: a systematic review and meta-analysis

机译:食管鳞状细胞癌患者mTOR和磷酸化mTOR表达的临床病理及预后意义:系统评价与荟萃分析

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Background Mammalian target of rapamycin (mTOR) is a serine/threonine protein kinase responsible for regulating ribosomal biogenesis and protein synthesis. Dysregulation of mTOR contributes to tumorigenesis, angiogenesis, cellular growth and metastasis but its roles in esophageal squamous cell carcinoma (ESCC) are controversial. Therefore, the objective of this study is to evaluate the prognostic and clinicopathological significance of mTOR/p-mTOR expression in ESCC. Methods Literature retrieval was conducted by searching PubMed, EMBASE and the Web of Science for full-text papers that met our eligibility criteria. Odds ratio (OR) and hazard ratio (HR) with 95?% confidence interval (CI) served as the appropriate summarized statistics for assessments of clinicopathological and prognostic significance, respectively. Cochrane Q-test and I2-statistic were adopted to estimate the heterogeneity level between studies. Potential publication bias was detected by Begg’s test and Egger’s test. Results A total of 915 ESCC patients from nine original articles were included into this meta-analysis. The pooled analyses suggested that mTOR/p-mTOR expression was significantly correlated with the unfavorable outcomes of differentiation degree (OR: 2.63; 95 % CI: 1.71–4.05; P =?0.001), tumor invasion (OR: 1.48; 95 % CI: 1.02–2.13; P =?0.037), TNM stage (OR: 2.25; 95 % CI: 1.05–4.82; P =?0.037) and lymph node metastasis (OR: 1.82; 95 % CI: 1.06–3.11; P =?0.029), but had no significant relationship to the genders (OR: 0.81; 95 % CI: 0.50–1.32; P =?0.396). Moreover, mTOR/p-mTOR expression could independently predict the worse overall survival (HR: 2.04; 95 % CI: 1.58–2.62; P Conclusions Positive expression of mTOR and p-mTOR was significantly associated with the unfavorable conditions on the depth of tumor invasion, TNM stage, differentiation degree and lymph node metastasis. mTOR and p-mTOR could serve as a valuable predictor for the poor prognosis of ESCC. More high-quality worldwide studies performing a multivariate analysis based on larger sample size are urgently required for further verifying and modifying our findings in the future.
机译:背景雷帕霉素的哺乳动物靶标(mTOR)是负责调节核糖体生物发生和蛋白质合成的丝氨酸/苏氨酸蛋白激酶。 mTOR失调有助于肿瘤发生,血管生成,细胞生长和转移,但其在食管鳞状细胞癌(ESCC)中的作用尚有争议。因此,本研究的目的是评估ESCC中mTOR / p-mTOR表达的预后和临床病理学意义。方法通过检索PubMed,EMBASE和Web of Science来检索符合我们资格标准的全文论文,以进行文献检索。具有95%置信区间(CI)的奇数比(OR)和危险比(HR)分别作为评估临床病理和预后意义的适当汇总统计数据。采用Cochrane Q检验和I 2 统计量估计研究之间的异质性水平。 Begg检验和Egger检验检测到潜在的出版偏倚。结果该荟萃分析纳入了来自9篇原创文章的915名ESCC患者。汇总分析表明,mTOR / p-mTOR表达与分化程度(OR:2.63; 95%CI:1.71-4.05; P =?0.001),肿瘤浸润(OR:1.48; 95%CI)的不良结局显着相关。 :1.02-2.13; P =?0.037),TNM分期(OR:2.25; 95%CI:1.05-4.82; P =?0.037)和淋巴结转移(OR:1.82; 95%CI:1.06-3.11; P = = 0.029),但与性别没有显着关系(OR:0.81; 95%CI:0.50-1.32; P = 0.396)。此外,mTOR / p-mTOR的表达可以独立预测较差的总生存期(HR:2.04; 95%CI:1.58–2.62; P结论)mTOR和p-mTOR的阳性表达与肿瘤深度的不利条件显着相关侵袭,TNM分期,分化程度和淋巴结转移,mTOR和p-mTOR可作为ESCC预后不良的有价值的预测指标,迫切需要更多高质量的全球研究,在更大样本量的基础上进行多因素分析。将来验证和修改我们的发现。

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