Department of General Surgery, First Hospital/First Clinical College of Shanxi Medical University, Taiyuan 030001, China.
Biosci Rep. 2020 Nov 27;40(11). doi: 10.1042/BSR20190372.
Long non-coding RNA (lncRNA) FOXD2 adjacent opposite strand RNA 1 (FOXD2-AS1) is aberrantly expressed in various cancers and associated with cancer progression. A comprehensive meta-analysis was performed based on published literature and data in the Gene Expression Omnibus database, and then the Cancer Genome Atlas (TCGA) dataset was used to assess the clinicopathological and prognostic value of FOXD2-AS1 in cancer patients.
Gene Expression Omnibus databases of microarray data and published articles were used for meta-analysis, and TCGA dataset was also explored using the GEPIA analysis program. Hazard ratios (HRs) and pooled odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the role of FOXD2-AS1 in cancers.
This meta-analysis included 21 studies with 2391 patients and 25 GEO datasets with 3311 patients. The pooled HRs suggested that highly expressed FOXD2-AS1 expression was correlated with poor overall survival (OS) and disease-free survival (DFS). Similar results were obtained by analysis of TCGA data for 9502 patients. The pooled results also indicated that FOXD2-AS1 expression was associated with bigger tumor size and advanced TNM stage, but was not related to age, gender, differentiation and lymph node metastasis.
The present study demonstrated that FOXD2-AS1 is closely related to tumor size and TNM stage. Additionally, increased FOXD2-AS1 was a risk factor of OS and DFS in cancer patients, suggesting FOXD2-AS1 may be a potential biomarker in human cancers.
长链非编码 RNA(lncRNA)叉头框蛋白 D2 反义链 RNA1(FOXD2-AS1)在多种癌症中异常表达,并与癌症进展相关。本研究基于已发表的文献和基因表达综合数据库中的数据进行了全面的荟萃分析,然后使用癌症基因组图谱(TCGA)数据集评估 FOXD2-AS1 在癌症患者中的临床病理和预后价值。
使用基因表达综合数据库中的微阵列数据和已发表的文章进行荟萃分析,并使用 GEPIA 分析程序探索 TCGA 数据集。使用风险比(HRs)和合并优势比(ORs)及其 95%置信区间(CIs)评估 FOXD2-AS1 在癌症中的作用。
本荟萃分析纳入了 21 项研究,共 2391 例患者和 25 个 GEO 数据集,共 3311 例患者。合并 HRs 表明,FOXD2-AS1 高表达与总生存期(OS)和无病生存期(DFS)不良相关。对 9502 例 TCGA 数据的分析也得到了类似的结果。合并结果还表明,FOXD2-AS1 表达与肿瘤较大和较晚的 TNM 分期有关,但与年龄、性别、分化和淋巴结转移无关。
本研究表明 FOXD2-AS1 与肿瘤大小和 TNM 分期密切相关。此外,FOXD2-AS1 增加是癌症患者 OS 和 DFS 的危险因素,提示 FOXD2-AS1 可能是人类癌症的潜在生物标志物。