RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Novel role of immune-related non-coding RNAs as potential biomarkers regulating tumour immunoresponse via MICA/NKG2D pathway.
Novel role of immune-related non-coding RNAs as potential biomarkers regulating tumour immunoresponse via MICA/NKG2D pathway.
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主要组织相容性复合体I类相关链A(MICA)是自然杀伤组2成员D受体(NKG2D)的一种重要的应激诱导型配体,在多种肿瘤细胞中表达。鉴于MICA/NKG2D信号系统深度参与固有免疫和适应性免疫应答,其尤其参与肿瘤和病毒感染的免疫监视。新出现的证据揭示了非编码RNA(ncRNA),包括microRNA(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、cancer和miRNAs在PubMed、Scopus和Web of Science数据库中检索了所有相关文献。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可靶向NKG2D mRNA和MICA mRNA的3‘非翻译区(3’-UTR),导致NKG2D翻译抑制和MICA降解。在miRNA表达异常的癌症中,若干免疫相关的MICA/NKG2D通路可能失调。
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mRNA抑制,从而诱导癌症中MICA的异常表达。本综述总结了由NK细胞和癌细胞介导的ncRNA相关MICA/NKG2D通路中免疫逃逸的新机制。
此外,我们鉴定了miRNA-NKG2D、miRNA-MICA和circRNA/lncRNA/mRNA-miRNA-mRNA/MICA轴。
因此,我们特别关注ncRNA对MICA/NKG2D通路中介导的免疫逃逸的调控,作为免疫和癌症的潜在治疗靶点和诊断生物标志物。
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.
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