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Effects of mesenchymal stem cells on solid tumor metastasis in experimental cancer models: a systematic review and meta-analysis

机译:间充质干细胞对实验性癌症模型实体瘤转移的影响:系统评价和荟萃分析

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It has been reported mesenchymal stem cells (MSCs) are recruited to and become integral parts of the tumor microenvironment. MSCs might have an active role in solid tumor progression, especially cancer metastasis. However, the contribution of MSCs in the process of cancer metastasis is still controversial. In this review, we performed a meta-analysis on the effects of MSCs administration on cancer metastasis based on published preclinical studies. The PRISMA guidelines were used. A total of 42 publications met the inclusion criteria. Outcome data on the incidence and the number of cancer metastasis as well as study characteristics were extracted. Quality of the studies was assessed according to SYRCLE Risk of Bias tool. Random-effects meta-analysis was used to pool estimates. Of the 42 studies included, 32 reported that MSCs administration promoted outcome events (numbers or incidences of cancer metastasis), and 39 reported data suitable for meta-analysis. The median effect size (RR) was 2.04 for the incidence of cancer metastasis (95% CI 1.57–2.65, I2?=?21%), and the median effect size (SMD) was 1.23 for the number of cancer metastasis (95% CI 0.43–2.03, I2?=?89%). Heterogeneity was observed, with the greater impact based on study length and different ways of metastasis measurement and MSCs administration. Our results suggested MSCs administration increased the number and the incidence of cancer metastasis in experimental cancer models. High heterogeneity and poor reported risk of bias limit the quality of these findings. Further preclinical studies with better design and adequate reporting are still needed.
机译:据报道,间充质干细胞(MSC)被募集并成为肿瘤微环境的组成部分。 MSC可能在实体瘤进展,特别是癌症转移中起积极作用。然而,MSCs在癌症转移过程中的作用仍存在争议。在这篇综述中,我们基于已发表的临床前研究对MSCs给药对癌症转移的影响进行了荟萃分析。使用了PRISMA指南。共有42篇出版物符合纳入标准。提取关于癌症转移的发生率和数量以及研究特征的结果数据。根据SYRCLE偏见风险工具评估研究质量。随机效应荟萃分析用于合并估计。在所包括的42项研究中,有32篇报道说MSCs的给药促进了结局事件(癌症转移的数量或发生率),还有39篇报道了适合进行荟萃分析的数据。癌症转移发生率的中值影响大小(RR)为2.04(95%CI 1.57–2.65,I2?=?21%),癌症转移发生率的中值影响大小(SMD)为1.23(95% CI 0.43–2.03,I2 == 89%)。观察到异质性,基于研究时间和转移测量的不同方式以及MSCs的使用,其影响更大。我们的结果表明,在实验性癌症模型中,MSCs的施用增加了癌症转移的数量和发生率。高度异质性和不良的偏见风险限制了这些发现的质量。仍需要具有更好设计和充足报告的进一步临床前研究。

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