cirglis3通过miR-146b-3p/AIF1L轴抑制甲状腺癌的侵袭转移。

IF 4.9 2区 医学 Q2 CELL BIOLOGY Cellular Oncology Pub Date : 2023-12-01 Epub Date: 2023-08-23 DOI:10.1007/s13402-023-00845-2
Siting Cao, Yali Yin, Huijuan Hu, Shubin Hong, Weiman He, Weiming Lv, Rengyun Liu, Yanbing Li, Shuang Yu, Haipeng Xiao
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引用次数: 0

摘要

目的:研究表明,circRNA参与了人类癌症的发生发展。然而,circRNA在甲状腺癌中的作用及其在肿瘤发生过程中的作用尚不清楚。方法:采用RNA测序法检测circRNA-miRNA-mRNA在甲状腺癌组织中的表达谱,并采用qRT-PCR方法进行验证。通过RNase R和放线菌素检测、亚细胞分离和荧光原位杂交验证了cirglis3的特性。采用创面愈合、transwell、3D培养和Western blot检测cirglis3和AIF1L的功能。采用RNA免疫沉淀(RIP)、RNA拉下和双荧光素酶报告基因法验证cirglis3和下游mirna的靶基因。通过转染靶基因的miRNA模拟物或siRNA进行功能挽救实验。最后,使用转移小鼠模型来研究circGLIS3在体内的功能。结果:本研究通过RNA测序发现了一种新的circRNA (has_circ_0007368,命名为circGLIS3)。CircGLIS3在甲状腺癌组织细胞系中表达下调,与甲状腺癌的恶性临床特征呈负相关。功能研究发现,cirglis3能够抑制甲状腺癌细胞的迁移和侵袭,并与EMT过程有关。机制上,cirglis3可以作为miR-146b-3p海绵,上调AIF1L基因的表达,抑制甲状腺癌的进展。结论:我们的研究确定了circGLIS3在甲状腺癌中是一种新的肿瘤抑制因子,表明circGLIS3有潜力作为甲状腺癌的诊断和预后标志物。
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CircGLIS3 inhibits thyroid cancer invasion and metastasis through miR-146b-3p/AIF1L axis.

Purpose: Studies have shown that circRNA is involved in the occurrence and development of human cancers. However, it remains unclear that the contribution of circRNA in thyroid carcinoma and its role in the process of tumorigenesis.

Methods: The expression profile of circRNA-miRNA-mRNA in thyroid carcinoma was detected by RNA sequencing and verified by qRT-PCR. The characteristics of circGLIS3 were verified by RNase R and actinomycin assays, subcellular fractionation, and fluorescence in situ hybridization. The functions of circGLIS3 and AIF1L were detected by wound healing, transwell, 3D culture and Western blot. RNA Immunoprecipitation (RIP), RNA pulldown and dual-luciferase reporter assays were used to verify the target genes of circGLIS3 and downstream miRNAs. Functional rescue experiments were performed by transfecting miRNA mimics or siRNA of target genes. Finally, metastatic mouse models were used to investigate circGLIS3 function in vivo.

Results: In this study, we discovered a novel circRNA (has_circ_0007368, named as circGLIS3) by RNA sequencing. CircGLIS3 was down-regulated in thyroid carcinoma tissues and cells line, and was negatively associated with malignant clinical features of thyroid carcinoma. Functional studies found that circGLIS3 could inhibit the migration and invasion of thyroid carcinoma cells, and was related to the EMT process. Mechanistically, circGLIS3 can upregulate the expression of the AIF1L gene by acting as a miR-146b-3p sponge to inhibit the progression of thyroid carcinoma.

Conclusion: Our study identified circGLIS3 as a novel tumor suppressor in thyroid cancer, indicating the potential of circGLIS3 as a promising diagnostic and prognostic marker for thyroid cancer.

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来源期刊
Cellular Oncology
Cellular Oncology ONCOLOGY-CELL BIOLOGY
CiteScore
10.30
自引率
1.50%
发文量
86
审稿时长
12 months
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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