Department of Radiotherapy, Guangxi Medical University Cancer Hospital, Nanning, People's Republic of China.
Department of Medical Oncology, Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, People's Republic of China.
Cancer Control. 2022 Jan-Dec;29:10732748221106268. doi: 10.1177/10732748221106268.
Pim-1 is overexpressed in cancer tissues and plays a vital role in carcinogenesis. However, its clinical significance in cancers is not fully verified by meta-analysis, especially in relation to prognosis and clinicopathological features.
Four databases, PubMed, Embase, Cochrane Library, and Web of Science, were searched. Literature screening and data extraction according to the inclusion and exclusion criteria. The quality of the included literatures was evaluated using the Newcastle-Ottawa scale and the data analysis was performed using STATA and Review Manager software.
15 articles were finally included for meta-analysis, involving 1651 patients. Effect-size pooling analysis showed that high Pim-1 was related to poor overall survival (OS) (HR 1.68 [95% CI 1.17-2.40], .004) and disease-free survival (DFS) (HR 2.15 [95 %CI 1.15-4.01], .000). Subgroup analysis indicated that the detection techniques of Pim-1 were the main sources of heterogeneity, and 2 literatures using quantitative polymerase chain reaction (qPCR) for Pim-1mRNA had high homogeneity (I = .0%, .321) in OS. Another 13 studies that applied immunohistochemistry (IHC) for Pim-1 protein had significant heterogeneity (I=82.2%, .000; I=92%, .000) in OS and DFS, respectively, and further analysis demonstrated that ethnicity, sample size, and histopathological origin were considered to be the main factors affecting their heterogeneity. In addition, high Pim-1 was associated with lymph node metastasis (OR 1.40 [95% CI 1.02-1.92], = .04), distant metastasis (OR 2.69 [95%CI 1.67-4.35], < .0001), and clinical stage III-IV (OR .7 [95% CI .50-.96, = .03). Sensitivity analysis suggested that the pooled results of each effect-size were stable and reliable, and there was no significant publication bias ( .138) in all included articles.
High Pim-1 can not only predict poor OS and DFS of cancer, but also help to infer the malignant clinical characteristics of tumor metastasis. Pim-1 may be a potential and promising biomarker for early diagnosis, prognostic analysis and targeted therapy of tumors.
Pim-1 在癌症组织中过度表达,在致癌作用中起着至关重要的作用。然而,其在癌症中的临床意义尚未通过荟萃分析充分验证,特别是在与预后和临床病理特征相关的方面。
我们检索了 PubMed、Embase、Cochrane 图书馆和 Web of Science 这四个数据库。根据纳入和排除标准进行文献筛选和数据提取。使用 Newcastle-Ottawa 量表评估纳入文献的质量,并使用 STATA 和 Review Manager 软件进行数据分析。
最终有 15 篇文章纳入荟萃分析,涉及 1651 名患者。效应大小合并分析表明,高 Pim-1 与较差的总生存期(OS)(HR 1.68 [95%CI 1.17-2.40],.004)和无病生存期(DFS)(HR 2.15 [95%CI 1.15-4.01],.000)相关。亚组分析表明,Pim-1 的检测技术是异质性的主要来源,并且有 2 篇使用定量聚合酶链反应(qPCR)检测 Pim-1mRNA 的文献在 OS 中具有高同质性(I =.0%,.321)。另外 13 项应用免疫组织化学(IHC)检测 Pim-1 蛋白的研究在 OS 和 DFS 中均具有显著的异质性(I=82.2%,.000;I=92%,.000),进一步分析表明,种族、样本量和组织病理学来源被认为是影响其异质性的主要因素。此外,高 Pim-1 与淋巴结转移(OR 1.40 [95%CI 1.02-1.92], =.04)、远处转移(OR 2.69 [95%CI 1.67-4.35], <.0001)和临床分期 III-IV(OR.7 [95%CI.50-.96, =.03)相关。敏感性分析表明,每个效应大小的汇总结果是稳定和可靠的,并且在所有纳入的文章中都没有显著的发表偏倚(.138)。
高 Pim-1 不仅可以预测癌症患者较差的 OS 和 DFS,还可以帮助推断肿瘤转移的恶性临床特征。Pim-1 可能是一种潜在的、有前途的肿瘤早期诊断、预后分析和靶向治疗的生物标志物。