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微小RNA-510-5p通过抑制SNHG15促进甲状腺癌细胞的增殖、迁移和侵袭。

microRNA-510-5p promotes thyroid cancer cell proliferation, migration, and invasion through suppressing SNHG15.

作者信息

Liu Yongcun, Li Junli, Li Meng, Li Feng, Shao Yuan, Wu Liping

机构信息

Department of Oncology, The First People's Hospital of Xianyang, Xianyang, Shaanxi, China.

Department of Ophthalmology, The First People's Hospital of Xianyang, Xianyang, Shaanxi, China.

出版信息

J Cell Biochem. 2019 Jul;120(7):11738-11744. doi: 10.1002/jcb.28454. Epub 2019 Feb 20.

DOI:10.1002/jcb.28454
PMID:30790329
Abstract

SNHG15 has been suggested to be correlated with clinical progression and prognosis, and function as tumor suppressive long noncoding RNA in thyroid cancer at our previous study. SNHG15 was proposed to be a potential target for miR-510-5p at LncBase Predicted database. Thus, the aim of this study was to explore the relationship between miR-510-5p and SNHG15 in thyroid cancer, and the clinical significance of miR-510-5p in patients with thyroid cancer. In our results, levels of miR-510-5p expression were increased in thyroid cancer tissues and cell lines compared with adjacent normal thyroid tissues and normal thyroid cell line, respectively. There was a statistically negative correlation between SNHG15 expression and miR-510-5p expression in thyroid cancer tissues. Moreover, miR-510-5p directly bound to SNHG15, and negatively regulated SNHG15 expression in thyroid cancer cells. Furthermore, miR-510-5p promoted thyroid cancer cell proliferation, migration, and invasion through suppressing SNHG15. Finally, high miR-510-5p expression was observed in tumor tissues with advanced clinical stage or lymph node metastasis. In conclusion, we provide evidence to support a pivotal role for miR-510-5p in regulating thyroid cancer cell proliferation, migration, and invasion.

摘要

在我们之前的研究中,已表明SNHG15与临床进展和预后相关,并在甲状腺癌中作为肿瘤抑制性长链非编码RNA发挥作用。在LncBase预测数据库中,SNHG15被认为是miR-510-5p的一个潜在靶点。因此,本研究的目的是探讨miR-510-5p与SNHG15在甲状腺癌中的关系,以及miR-510-5p在甲状腺癌患者中的临床意义。在我们的研究结果中,与相邻正常甲状腺组织和正常甲状腺细胞系相比,甲状腺癌组织和细胞系中miR-510-5p的表达水平分别升高。在甲状腺癌组织中,SNHG15表达与miR-510-5p表达之间存在统计学上的负相关。此外,miR-510-5p直接与SNHG15结合,并在甲状腺癌细胞中负调控SNHG15的表达。此外,miR-510-5p通过抑制SNHG15促进甲状腺癌细胞的增殖、迁移和侵袭。最后,在临床分期较晚或有淋巴结转移的肿瘤组织中观察到miR-510-5p高表达。总之,我们提供的证据支持miR-510-5p在调节甲状腺癌细胞增殖、迁移和侵袭中起关键作用。

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