CircRNA has_circ_0069313在OSCC细胞和Treg细胞中通过miR-325-3p-Foxp3轴诱导OSCC免疫逃逸

Yiyang Chen, Zeyu Li, Jianfeng Liang, Jiayu Liu, J. Hao, Q. Wan, Jiameng Liu, Chongdai Luo, Zhiyuan Lu
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引用次数: 11

摘要

CircRNAs参与口腔鳞癌细胞(OSCC)的肿瘤发生和进展。然而,circRNAs在肿瘤相关免疫逃逸中的功能和潜在机制在很大程度上是未知的。材料和方法:我们分析了has_circ_0069313在我们内部数据库中的表达模式及其与OSCC预后的关系。免疫组化检测PDL1表达。应用RNA荧光原位杂交技术检测circRNA的亚细胞定位。荧光素酶活性测定用于检测has_circ_0069313与miR-325-3p及其下游靶点Foxp3的相互作用。收集外泌体以检测外泌体环状rna,并进行共培养试验以检测外泌体环状rna对Tregs的功能。结果:has_circ_0069313在OSCC组织中表达上调,预示预后不良。has_circ_0069313通过抑制mir -325-3p诱导的Foxp3降解促进免疫逃逸。has_circ_0069313是外泌体circRNA,将has_circ_0069313转移到Treg细胞中通过维持Foxp3水平来促进Treg功能。结论:我们的研究结果表明,has_circ_0069313通过miR-325-3p-Foxp3轴诱导OSCC细胞和Treg细胞的OSCC免疫逃逸。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CircRNA has_circ_0069313 induced OSCC immunity escape by miR-325-3p-Foxp3 axes in both OSCC cells and Treg cells
Introduction: CircRNAs are engaged in the tumorigenesis and progression of oral squamous cancer cells (OSCC). However, the function and underlying mechanism of circRNAs on tumor-associated immunity escape are largely unknown. Materials and methods: We analyzed the expression pattern of has_circ_0069313 in our in-house database and its correlation with OSCC prognosis. Immunohistochemistry was applied to detected PDL1 expression. RNA fluorescence in situ hybridization was applied to detect subcellular location of circRNA. A luciferase activity assay was used to detect the interaction of has_circ_0069313 and miR-325-3p and its downstream target, Foxp3. Exosomes were collected to detect the exosomal circRNAs and co-culture assays were performed to detect the function of exosomal circRNAs on Tregs. Results: has_circ_0069313 was upregulated in OSCC tissues and predicts poor prognosis. has_circ_0069313 promotes immunity escape through inhibiting miR-325-3p-induced Foxp3 degradation. has_circ_0069313 is an exosomal circRNA and the transfer of has_circ_0069313 to Treg cells promotes the Treg function through maintaining Foxp3 levels. Conclusion: Our results indicate that has_circ_0069313 induces OSCC immunity escape via the miR-325-3p-Foxp3 axis in both OSCC cells and Treg cells.
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