首页> 美国卫生研究院文献>Molecular Therapy. Nucleic Acids >Circular RNA circFOXM1 Plays a Role in Papillary Thyroid Carcinoma by Sponging miR-1179 and Regulating HMGB1 Expression
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Circular RNA circFOXM1 Plays a Role in Papillary Thyroid Carcinoma by Sponging miR-1179 and Regulating HMGB1 Expression

机译:环状RNA circFOXM1通过使miR-1179变海绵并调节HMGB1表达在乳头状甲状腺癌中发挥作用

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摘要

Circular RNAs (circRNAs) are a class of noncoding RNAs broadly expressed in cells of various species. However, the molecular mechanisms that link circRNAs with progression of papillary thyroid carcinoma (PTC) are not well understood. In the present study, we attempted to provide a novel basis for targeted therapy for PTC from the aspect of the circRNA-microRNA (miRNA)-mRNA interaction. We investigated the expression of circRNAs in five paired PTC tissues and normal tissues by microarray analysis. The circRNA microarray assay followed by qRT-PCR was used to verify the differential expression of circFOXM1 (hsa_circ_0025033), which is located at chr12: 2966846-2983691 and derived from FOXM1. The spliced length of circFOXM1 is 3410 nt. The qRT-PCR analysis was to investigate the expression pattern of circFOXM1 in PTC tissues and cell lines. Then, the effects of circFOXM1 on tumor growth were assessed in PTC and . Furthermore, bioinformatics online programs predicted, and the luciferase reporter assay was used to validate the association of circFOXM1 and miR-1179 in PTC cells. In this study, circFOXM1 was observed to be upregulated in PTC tissues and cell lines. circFOXM1 downregulation inhibited tumor growth of PTC and . Bioinformatics analysis predicted that there is a circFOXM1/miR-1179/high-mobility group box 1 (HMGB1) axis in PTC. A dual luciferase reporter system validated the direct interaction of circFOXM1, miR-1179, and HMGB1. In summary, our study demonstrated that circFOXM1 modulates cancer progression through the miR-1179/HMGB1 pathway in PTC. Our findings indicate that circFOXM1 may serve as a promising therapeutic target for the treatment of PTC patients.
机译:环状RNA(circRNA)是在各种物种的细胞中广泛表达的一类非编码RNA。然而,尚不清楚将circRNA与甲状腺乳头状癌(PTC)的进展联系起来的分子机制。在本研究中,我们尝试从circRNA-microRNA(miRNA)-mRNA相互作用的方面为PTC的靶向治疗提供新的基础。我们通过芯片分析研究了circRNA在五对成对的PTC组织和正常组织中的表达。使用circRNA微阵列测定法以及随后的qRT-PCR来验证circFOXM1(hsa_circ_0025033)的差异表达,其位于chr12:2966846-2983691,来自FOXM1。 circFOXM1的拼接长度为3410 nt。 qRT-PCR分析旨在研究circFOXM1在PTC组织和细胞系中的表达模式。然后,在PTC和中评估circFOXM1对肿瘤生长的影响。此外,预测了生物信息学在线程序,并使用萤光素酶报告基因分析验证了PTC细胞中circFOXM1和miR-1179的关联。在这项研究中,观察到circFOXM1在PTC组织和细胞系中被上调。 circFOXM1的下调抑制了PTC和ET的肿瘤生长。生物信息学分析预测,PTC中存在circFOXM1 / miR-1179 /高迁移率族框1(HMGB1)轴。双荧光素酶报告系统验证了circFOXM1,miR-1179和HMGB1的直接相互作用。总之,我们的研究表明circFOXM1通过PTC中的miR-1179 / HMGB1途径调节癌症进展。我们的发现表明,circFOXM1可以作为治疗PTC患者的有希望的治疗靶点。

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