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免疫相关非编码RNA作为通过MICA/NKG2D途径调节肿瘤免疫反应的潜在生物标志物的新作用。

Novel role of immune-related non-coding RNAs as potential biomarkers regulating tumour immunoresponse via MICA/NKG2D pathway.

作者信息

Zhang Jing, Luo Qizhi, Li Xin, Guo Junshuang, Zhu Quan, Lu Xiaofang, Wei Leiyan, Xiang Zhiqing, Peng Manqing, Ou Chunlin, Zou Yizhou

机构信息

Department of Pathology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.

Department of Immunology, School of Basic Medicine, Central South University, Changsha, 410000, Hunan, China.

出版信息

Biomark Res. 2023 Oct 2;11(1):86. doi: 10.1186/s40364-023-00530-4.

Abstract

Major histocompatibility complex class I related chain A (MICA) is an important and stress-induced ligand of the natural killer group 2 member D receptor (NKG2D) that is expressed in various tumour cells. Given that the MICA/NKG2D signalling system is critically embedded in the innate and adaptive immune responses, it is particularly involved in the surveillance of cancer and viral infections. Emerging evidence has revealed the important roles of non-coding RNAs (ncRNAs) including microRNAs (miRNAs), long noncoding RNAs (lncRNAs) and circular RNAs (circRNAs) in different cancer types. We searched for all relevant publications in the PubMed, Scopus and Web of Science database using the keywords ncRNA, MICA, NKG2D, cancer, and miRNAs. All relevant studies published from 2008 to the 2023 were retrieved and collated. Notably, we found that miRNAs can target to NKG2D mRNA and MICA mRNA 3'-untranslated regions (3'-UTR), leading to translation inhibition of NKG2D and MICA degradation. Several immune-related MICA/NKG2D pathways may be dysregulated in cancer with aberrant miRNA expressions. At the same time, the competitive endogenous RNA (ceRNA) hypothesis holds that circRNAs, lncRNAs, and mRNAs induce an abnormal MICA expression by directly targeting downstream miRNAs to mediate mRNA suppression in cancer. This review summarizes the novel mechanism of immune escape in the ncRNA-related MICA/NKG2D pathway mediated by NK cells and cancer cells. Moreover, we identified the miRNA-NKG2D, miRNA-MICA and circRNA/lncRNA/mRNA-miRNA-mRNA/MICA axis. Thus, we were particularly concerned with the regulation of mediated immune escape in the MICA/NKG2D pathway by ncRNAs as potential therapeutic targets and diagnostic biomarkers of immunity and cancer.

摘要

主要组织相容性复合体I类相关链A(MICA)是自然杀伤细胞2族成员D受体(NKG2D)的一种重要的应激诱导配体,在各种肿瘤细胞中表达。鉴于MICA/NKG2D信号系统在先天性和适应性免疫反应中起着关键作用,它尤其参与癌症和病毒感染的监测。新出现的证据揭示了非编码RNA(ncRNA),包括微小RNA(miRNA)、长链非编码RNA(lncRNA)和环状RNA(circRNA)在不同癌症类型中的重要作用。我们使用关键词ncRNA、MICA、NKG2D、癌症和miRNA在PubMed、Scopus和Web of Science数据库中搜索了所有相关出版物。检索并整理了2008年至2023年发表的所有相关研究。值得注意的是,我们发现miRNA可以靶向NKG2D mRNA和MICA mRNA的3'非翻译区(3'-UTR),导致NKG2D的翻译抑制和MICA降解。在具有异常miRNA表达的癌症中,一些免疫相关的MICA/NKG2D途径可能失调。同时,竞争性内源RNA(ceRNA)假说认为,circRNA、lncRNA和mRNA通过直接靶向下游miRNA来介导癌症中的mRNA抑制,从而诱导MICA异常表达。本综述总结了由自然杀伤细胞和癌细胞介导的ncRNA相关MICA/NKG2D途径中免疫逃逸的新机制。此外,我们确定了miRNA-NKG2D、miRNA-MICA和circRNA/lncRNA/mRNA-miRNA-mRNA/MICA轴。因此,我们特别关注ncRNA对MICA/NKG2D途径中介导的免疫逃逸的调节,将其作为免疫和癌症的潜在治疗靶点和诊断生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cbc/10546648/8c2aa2ed39fa/40364_2023_530_Fig1_HTML.jpg

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