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微小 RNA 与人类疾病中 B7 家族新成员之间的调控串扰:范围综述。

The Regulatory Cross-Talk between microRNAs and Novel Members of the B7 Family in Human Diseases: A Scoping Review.

机构信息

Department of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz 5166616471, Iran.

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz 5165665811, Iran.

出版信息

Int J Mol Sci. 2021 Mar 6;22(5):2652. doi: 10.3390/ijms22052652.

DOI:10.3390/ijms22052652
PMID:33800752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962059/
Abstract

The members of the B7 family, as immune checkpoint molecules, can substantially regulate immune responses. Since microRNAs (miRs) can regulate gene expression post-transcriptionally, we conducted a scoping review to summarize and discuss the regulatory cross-talk between miRs and new B7 family immune checkpoint molecules, i.e., B7-H3, B7-H4, B7-H5, butyrophilin like 2 (BTNL2), B7-H6, B7-H7, and immunoglobulin like domain containing receptor 2 (ILDR2). The current study was performed using a six-stage methodology structure and Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guideline. PubMed, Embase, Scopus, Cochrane, ProQuest, and Google Scholar were systematically searched to obtain the relevant records to 5 November 2020. Two authors independently reviewed the obtained records and extracted the desired data. After quantitative and qualitative analyses, we used bioinformatics approaches to extend our knowledge about the regulatory cross-talk between miRs and the abovementioned B7 family members. Twenty-seven articles were identified that fulfilled the inclusion criteria. Studies with different designs reported gene-miR regulatory axes in various cancer and non-cancer diseases. The regulatory cross-talk between the aforementioned B7 family molecules and miRs might provide valuable insights into the pathogenesis of various human diseases.

摘要

B7 家族成员作为免疫检查点分子,可以显著调节免疫反应。由于 microRNAs(miRs)可以在后转录水平上调节基因表达,我们进行了范围综述,以总结和讨论 miR 与新的 B7 家族免疫检查点分子(即 B7-H3、B7-H4、B7-H5、butyrophilin like 2(BTNL2)、B7-H6、B7-H7 和免疫球蛋白样结构域受体 2(ILDR2))之间的调控交叉对话。本研究使用六阶段方法结构和系统评价和荟萃分析的首选报告项目(PRISMA)指南进行。系统检索了 PubMed、Embase、Scopus、Cochrane、ProQuest 和 Google Scholar,以获取截至 2020 年 11 月 5 日的相关记录。两名作者独立审查了获得的记录并提取了所需的数据。经过定量和定性分析,我们使用生物信息学方法扩展了我们对 miR 与上述 B7 家族成员之间调控交叉对话的了解。确定了 27 篇符合纳入标准的文章。具有不同设计的研究在各种癌症和非癌症疾病中报告了基因-miR 调节轴。上述 B7 家族分子与 miR 之间的调控交叉对话可能为各种人类疾病的发病机制提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/1a324ceb9630/ijms-22-02652-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/34dab571e5f8/ijms-22-02652-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/efb1243995ce/ijms-22-02652-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/1a324ceb9630/ijms-22-02652-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/34dab571e5f8/ijms-22-02652-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/efb1243995ce/ijms-22-02652-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/609a/7962059/1a324ceb9630/ijms-22-02652-g003.jpg

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