Sun Zhenqiang, Xu Ruiwei, Li Xiayu, Ren Weiguo, Ou Chunlin, Wang Qisan, Zhang Han, Zhang Xuemei, Ma Jian, Wang Haijiang, Li Guiyuan
Key Laboratory of Carcinogenesis of Ministry of Health and Key Laboratory of Carcinogenesis and Cancer Invasion of Ministry of Education, Cancer Research Institute, Central South University, Changsha, Hunan, China; Department of Gastrointestinal Surgery, Affiliated Tumor Hospital, Xinjiang Medical University, Urumqi, Xinjiang, China.
Department of Epidemiology and Health Statistics, School of Public Health, Central South University, Changsha, Hunan, China; Department of Infection Control, Affiliated Tumor Hospital, Xinjiang Medical University, Urumqi, Xinjiang, China.
PLoS One. 2015 Aug 11;10(8):e0135119. doi: 10.1371/journal.pone.0135119. eCollection 2015.
Yes-associated protein 1 (YAP1) is an effector of Hippo pathway, which is critical for regulating organ size, cell proliferation and tumor growth in mammals. Many previous studies have explored the relationship between YAP1 and various types of cancer. However, these studies were limited by the small samples size and the findings were inconsistent among them. Therefore, a meta-analysis was conducted to assess the association between YAP1 and malignancies.
A systematic literature search was conducted for eligible studies in the PubMed, Corchane Library, Web of Knowledge, EMBASE and CBM disc databases from inception to August 1st 2014. After heterogeneity analysis, pooled harzad ratio (HR) with 95% confidence interval (95%CI) using both fixed and random effect models were estimated in STATA 10.0. Meta regression analysis, subgroup analysis and sensitivity analysis were performed to explore the potential sources of heterogeneity and to evaluate the robustness of the result. Publication bias was assessed by Egger's test and funnel plot.
A total of 21 unique articles from 2009 to 2014, comprising 2983 patients, were analyzed in the meta-analysis. The association of YAP1 expression and overall survival time (OS) was evaluated in 20 studies including 2067 patients. Positive YAP1 showed poorer OS (HR = 1.826; 95% CI = 1.465-2.275; p <0.002). For evaluating disease-free survival time (DFS), 10 studies with 1139 patients were analyzed. Positive YAP1 indicated worse DFS (HR = 2.114; 95%CI = 1.406-3.179; p <0.001). Subgroup analysis showed that both positive nuclear YAP1 (HR = 1.390, 95% CI: 0.810-2.400, p = 0.729) and up-regulation overall YAP1 (HR = 2.237, 95% CI: 1.548-3.232, p <0.001) had poorer OS for patients with malignancies. Similarly, both positive nuclear YAP1 (HR = 3.733, 95% CI: 1.469-9.483, p = 0.001) and up-regulation overall YAP1 (HR = 1.481, 95% CI: 1.163-1.886, p = 0.554) showed worse DFS. The patients with urogenital system cancer had the poorest OS (HR = 2.133, 95% CI: 1.549-2.937, p = 0.020). The patients with alimentary system cancer had the most significant impact on DFS (HR = 1.879, 95% CI: 1.537-2.297, p <0.001).
Both overall and nuclear YAP1 overexpression are intimately associated with adverse OS and DFS in numerous cancers, suggesting that YAP1 may act as a potential therapeutic targets of these malignancies in the future.
Yes相关蛋白1(YAP1)是Hippo信号通路的效应器,对调节哺乳动物器官大小、细胞增殖和肿瘤生长至关重要。此前许多研究探讨了YAP1与各类癌症之间的关系。然而,这些研究受限于样本量小,且研究结果相互矛盾。因此,进行了一项荟萃分析以评估YAP1与恶性肿瘤之间的关联。
对PubMed、考克兰图书馆、Web of Knowledge、EMBASE和CBM disc数据库中从建库至2014年8月1日的符合条件的研究进行系统文献检索。经过异质性分析,在STATA 10.0中使用固定效应模型和随机效应模型估计合并风险比(HR)及95%置信区间(95%CI)。进行Meta回归分析、亚组分析和敏感性分析以探索异质性的潜在来源并评估结果的稳健性。通过Egger检验和漏斗图评估发表偏倚。
荟萃分析共纳入了2009年至2014年的21篇独立文章,包含2983例患者。在包括2067例患者的20项研究中评估了YAP1表达与总生存时间(OS)的关联。YAP1阳性者的OS较差(HR = 1.826;95%CI = 1.465 - 2.275;p <0.002)。对于评估无病生存时间(DFS),分析了10项研究中的1139例患者。YAP1阳性提示DFS较差(HR = 2.114;95%CI = 1.406 - 3.179;p <0.001)。亚组分析显示,核YAP1阳性(HR = 1.390,95%CI:0.810 - 2.400,p = 0.729)和YAP1整体上调(HR = 2.237,95%CI:1.548 - 3.232,p <0.001)的恶性肿瘤患者OS均较差。同样,核YAP1阳性(HR = 3.733,95%CI:1.469 - 9.483,p = 0.001)和YAP1整体上调(HR = 1.481,95%CI:1.163 - 1.886,p = 0.554)均显示DFS较差。泌尿生殖系统癌症患者的OS最差(HR = 2.133,95%CI:1.549 - 2.937,p = 0.020)。消化系统癌症患者对DFS的影响最为显著(HR = 1.879,95%CI:1.537 - 2.297,p <0.001)。
YAP1整体及核过表达均与多种癌症的不良OS和DFS密切相关,提示YAP1未来可能成为这些恶性肿瘤的潜在治疗靶点。