MicroRNA- 103 as a novel potential biomarker of poor prognosis and durg resistance in solid tumours.

IF 2.9 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Xiaoping Xia, Xiuping Weng, Tianyu Liang, Mingxia Xu, Chao Zhang
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Abstract

Backgroud: 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.

Methods: 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.

Results: 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).

Conclusion: 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.

MicroRNA- 103作为实体肿瘤不良预后和耐药的潜在生物标志物。
背景:已有多项研究报道,microRNA-103在多种肿瘤中不受调控,参与肿瘤发生,并与肿瘤预后相关,因此我们通过系统综述和荟萃分析来确定microRNA-103与实体瘤预后的关系。方法:检索PubMed、Web of Science和EMBASE数据库,检索相关文章,确定microRNA-103与肿瘤预后的关系。根据纽卡斯尔-渥太华量表(NOS)对相关文章进行评分。采用固定效应/随机效应模型计算95%置信区间(CI),并总结风险比(RR)。结果:162篇检索文献中有8篇纳入本综述,NOS平均评分为7.2分。4项组织样本研究和4项血清样本研究表明,microRNA-103过表达与总生存率相关(RR = 2.65, 95% CI: 1.79 ~ 3.93, P = 0.000; RR = 3.31, 95% CI: 2.04 ~ 5.36, P = 0.000)。结论:本荟萃分析结合9项研究发现,miRNA-103过表达与实体肿瘤的不良预后相关,特别是在血清样本中。敏感性分析证实,高组织表达与不良预后相关。miRNA-103在肿瘤进展中的作用表明其作为实体肿瘤预后生物标志物的潜力,值得进一步研究临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
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