Department of Hepatic-Biliary-Pancreatic Surgery, The First people's Hospital of Neijiang, Neijiang, Sichuan, China.
Medicine (Baltimore). 2021 Dec 23;100(51):e28425. doi: 10.1097/MD.0000000000028425.
ArfGAP with GTPase domain, Ankyrin repeat and PH domain 2 Antisense 1 (AGAP2-AS1) is a promising long noncoding RNA that may possess prognostic value for different types of tumors. The objective of this meta-analysis is to evaluate the prognostic value of long noncoding RNA AGAP2-AS1 in cancer patients.
A systematic literature search of the PubMed, Cochrane Library, EMBASE, Medline, Web of Science, CNKI, Weipu, and Wanfang electronic databases were carried out in this meta-analysis. Synthetic hazard ratios (HRs) or odd ratios (ORs) with 95% confidence intervals (CIs) were obtained to determine the prognostic and clinicopathological significance of AGAP2-AS1 expression in tumors.
The final meta-analysis included 10 studies that contained 948 patients. The pooled results provided evidence that AGAP2-AS1 overexpression predicted reduced overall survival (OS) (HR = 1.77, 95% CI: 1.49-2.09, P < .00001), disease-free survival (HR = 1.84, 95% CI: 1.40-2.41, P < .0001), and progression-free survival (HR = 1.84, 95% CI: 1.01-3.33, P = .04) and for various cancers. Additionally, the AGAP2-AS1 overexpression was concerned with lymph node metastasis (positive vs negative, OR = 2.95, 95% CI: 1.96-4.45, P < .00001), advanced tumor node metastasis stage (III/IV vs I/II, OR = 3.73, 95% CI: 2.71-5.13, P < .00001), and tumor size (larger vs smaller, OR = 2.28, 95% CI: 1.24-4.18, P = .008). Besides, data from gene expression profiling interactive analysis dataset verified the results in our meta-analysis. The results showed that the expression level of AGAP2-AS1 was higher in most tumor tissues than in the corresponding normal tissues and was linked to poor OS and disease-free survival.
Our results indicated that AGAP2-AS1 overexpression was closely correlated with shorter OS in multiple cancer types, suggesting that AGAP2-AS1 might function as a promising predictor for clinical outcomes in cancer.
ArfGAP 与 GTPase 结构域、锚蛋白重复和 PH 结构域 2 反义 1(AGAP2-AS1)是一种有前途的长非编码 RNA,可能对不同类型的肿瘤具有预后价值。本荟萃分析的目的是评估长非编码 RNA AGAP2-AS1 在癌症患者中的预后价值。
本荟萃分析系统地检索了 PubMed、Cochrane 图书馆、EMBASE、Medline、Web of Science、CNKI、维普和万方电子数据库。使用合成风险比(HR)或优势比(OR)及其 95%置信区间(CI)来确定 AGAP2-AS1 表达在肿瘤中的预后和临床病理意义。
最终的荟萃分析纳入了 10 项研究,共包含 948 名患者。汇总结果表明,AGAP2-AS1 过表达预示着总生存期(OS)(HR=1.77,95%CI:1.49-2.09,P<0.00001)、无病生存期(DFS)(HR=1.84,95%CI:1.40-2.41,P<0.0001)和无进展生存期(PFS)(HR=1.84,95%CI:1.01-3.33,P=0.04)降低,适用于各种癌症。此外,AGAP2-AS1 过表达与淋巴结转移(阳性与阴性,OR=2.95,95%CI:1.96-4.45,P<0.00001)、肿瘤淋巴结转移分期(III/IV 期与 I/II 期,OR=3.73,95%CI:2.71-5.13,P<0.00001)和肿瘤大小(较大与较小,OR=2.28,95%CI:1.24-4.18,P=0.008)有关。此外,来自基因表达谱交互分析数据集的数据验证了我们荟萃分析中的结果。结果表明,AGAP2-AS1 在大多数肿瘤组织中的表达水平高于相应的正常组织,与较差的 OS 和无病生存期相关。
我们的结果表明,AGAP2-AS1 过表达与多种癌症类型的 OS 缩短密切相关,表明 AGAP2-AS1 可能是癌症临床结局的一个有前途的预测因子。