Chaomin Pan, Zhuoyu Ding, Jingping Dai, Li Yang, Yiyi Wei, Xinke Wang
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引用次数: 0
摘要
环状rna (circRNAs)与癌症的增殖、迁移和侵袭有关。在众多circrna中,circSMARAC5引起了我们的极大关注。本研究旨在拓宽对circSMARCA5的认识,探索其在实体瘤临床病理和治疗中的功能。纳入的研究通过Web of Science, PubMed, Embase和Cochrane Library进行了探索,包括1048名患者。本研究使用STATA 12.0和Review Manager 5.3软件进行计算。临床病理特征和治疗靶点分析采用合并奇数比(or)和95%可信区间(ci)。利用Cytoscape 3.9.0构建circSMARCA5的ceRNA网络。最终有8项研究被纳入临床病理特征,4篇文献被用于探索治疗靶点。circSMARCA5低表达患者与性别(OR = 1.367, 95% CI = 1.003 ~ 1.862, p = 0.048)和病理分化(OR = 1.627, 95% CI = 1.130 ~ 2.343, p = 0.009)密切相关。在这些调节轴中,最常见的microRNA是miR‐432。在不久的将来,circSMARCA5可能成为一种有前景的诊断生物标志物和新的治疗靶点。
CircSMARCA5 functions as a potential biomarker for clinicopathology and therapy in solid tumors: A systematic review and meta‐analysis
Circular RNAs (circRNAs) have been implicated in cancer proliferation, migration, and invasion. Among various circRNAs, circSMARAC5 attracted our great attention. The research aimed at broadening the knowledge on circSMARCA5 and exploring its function in clinicopathology and therapy in solid tumors. The incorporated research was explored via Web of Science, PubMed, Embase, and Cochrane Library, consisting of 1048 patients. This study was calculated using STATA 12.0 and Review Manager 5.3 software. Clinicopathological characteristics and therapeutic targets were analyzed using pooled odd ratios (ORs) with 95% confidence intervals (CIs). And the ceRNA network of circSMARCA5 was constructed via Cytoscape 3.9.0. Eventually, there were eight studies included in conducting clinicopathological characteristics and four literature used in exploring therapeutic targets. Patients with low expression of circSMARCA5 were closely associated with gender (OR = 1.367, 95% CI = 1.003–1.862, p = .048) and pathological differentiation (OR = 1.627, 95% CI = 1.130–2.343, p = .009). Among these modulating axes, the most commonly microRNA was miR‐432. In the near future, circSMARCA5 may be a promising diagnostic biomarker and a new therapeutic target.