LRP11-AS1的下调通过调节miR-615-3p/AKT2轴抑制甲状腺乳头状肿瘤的生长。

IF 4.1 2区 医学 Q1 ONCOLOGY
Peng Li, Zhongguang Wu, Lanlan Li, Yudan Chen, Chi Zhang, Weidong Zheng
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引用次数: 0

摘要

甲状腺乳头状癌(PTC)发生局部复发和远处转移的患者临床预后差,生存率低。在本研究中,我们评估了LRP11-AS1在甲状腺乳头状癌患者组织样本和PTC细胞系中的表达。我们观察到LRP11-AS1在PTC组织和PTC细胞系中均显著过表达,LRP11-AS1敲低对PTC细胞的生长和迁移有抑制作用。机制上,LRP11-AS1的敲低导致miR-615-3p的上调,miR-615-3p的过表达降低LRP11-AS1和AKT2的表达。双荧光素酶报告基因实验证实了miR-615-3p对LRP11-AS1和AKT2表达的抑制作用。LRP11-AS1基因敲低可抑制裸鼠PTC肿瘤的体内生长。LRP11-AS1通过调节miR-615-3p/AKT2轴在PTC中表现出潜在的致癌作用,提示LRP11-AS1可以作为PTC的潜在诊断生物标志物和治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Knockdown of LRP11-AS1 inhibits papillary thyroid tumor growth by modulating miR-615-3p/AKT2 axis.

Patients with papillary thyroid cancer (PTC) who experience local recurrence and distant metastases have a poor clinical prognosis and low survival rate. In this study, the expression of LRP11-AS1 was evaluated in both tissue samples from patients with papillary thyroid cancer and in PTC cell lines. We observed significant overexpression of LRP11-AS1 in both PTC tissues and PTC cell lines and inhibitory effects of LRP11-AS1 knockdown on the growth and migration of PTC cells. Mechanistically, knockdown of LRP11-AS1 led to upregulation of miR-615-3p, overexpression of miR-615-3p decreased the expression of both LRP11-AS1 and AKT2. The dual-luciferase reporter assay confirmed the inhibitory effect of miR-615-3p on the expression of LRP11-AS1 and AKT2. Knockdown of LRP11-AS1 inhibited in vivo growth of PTC tumor in nude mice model. LRP11-AS1 exhibited potential oncogenic effects in PTC by regulating the miR-615-3p/AKT2 axis, suggesting that LRP11-AS1 could serve as a potential diagnostic biomarker and therapeutic target in PTC.

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来源期刊
Translational Oncology
Translational Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
7.20
自引率
2.00%
发文量
314
审稿时长
6-12 weeks
期刊介绍: Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.
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