Xia Xiaoping, Weng Xiuping, Liang Tianyu, Xu Mingxia, Zhang Chao
Department of Intensive Care Unit, Taizhou Integrated Traditional Chinese and Western Medicine Hospital, Wenling, Zhejiang Province, China.
General Surgery, Cancer Center, Department of Gastrointestinal and Pancreatic Surgery, Department of nursing, Affiliated People's Hospital, Zhejiang Provincial People's Hospital, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Discov Oncol. 2025 Jun 22;16(1):1177. doi: 10.1007/s12672-025-02963-9.
Multiple studies have reported that microRNA-103 is unregulated in a variety of tumours, involved in tumorigenesis, and associated with tumour prognosis, so a systematic review and meta-analysis were performed to determine the relationship between microRNA-103 and the prognosis of solid tumours.
The PubMed, Web of Science, and EMBASE databases were searched to retrieve articles to determine the relationship between microRNA-103 and tumour prognosis. Relevant articles were graded according to the Newcastle-Ottawa Scale (NOS). The 95% confidence interval (CI) was calculated by the fixed-effect/random-effect models and the risk ratio (RR) were summarised.
Eight out of 162 retrieved articles were included in this review, with an average NOS score of 7.2 points. Four studies of tissue samples and four studies of serum samples suggested that the overexpression of microRNA-103 was associated with overall survival (RR = 2.65, 95% CI: 1.79-3.93, P = 0.000 and RR = 3.31, 95% CI: 2.04-5.36, P = 0.000, respectively).
This meta-analysis, combining 9 studies, found that overexpression of miRNA-103 is associated with poor prognosis in solid tumours, particularly in serum samples. Sensitivity analysis confirmed that high tissue expression correlates with poor outcomes. miRNA-103's role in tumor progression suggests its potential as a prognostic biomarker for solid tumors, warranting further research for clinical applications.
多项研究报告称,微小RNA-103在多种肿瘤中表达失调,参与肿瘤发生,并与肿瘤预后相关,因此进行了一项系统评价和荟萃分析,以确定微小RNA-103与实体瘤预后之间的关系。
检索PubMed、Web of Science和EMBASE数据库,以检索确定微小RNA-103与肿瘤预后关系的文章。相关文章根据纽卡斯尔-渥太华量表(NOS)进行分级。采用固定效应/随机效应模型计算95%置信区间(CI),并汇总风险比(RR)。
162篇检索到的文章中有8篇纳入本评价,平均NOS评分为7.2分。四项组织样本研究和四项血清样本研究表明,微小RNA-103的过表达与总生存期相关(RR分别为2.65,95%CI:1.79-3.93,P = 0.000;RR为3.31,95%CI:2.04-5.36,P = 0.000)。
这项荟萃分析结合了9项研究,发现miRNA-103的过表达与实体瘤预后不良相关,尤其是在血清样本中。敏感性分析证实,组织高表达与不良结局相关。miRNA-103在肿瘤进展中的作用表明其作为实体瘤预后生物标志物的潜力,值得进一步开展临床应用研究。