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长链非编码 RNA SNHG15 通过靶向 microRNA-211-3p 促进肺癌的增殖和迁移。

LncRNA SNHG15 promotes proliferation and migration of lung cancer via targeting microRNA-211-3p.

机构信息

Department of Thoracic Surgery, Affiliated Hospital of Weifang Medical University, Weifang, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Oct;22(20):6838-6844. doi: 10.26355/eurrev_201810_16152.

Abstract

OBJECTIVE

To investigate whether lncRNA (long non-coding RNA) SNHG15 could regulate the proliferation and migration of lung cancer via microRNA-211-3p and its underlying mechanism.

PATIENTS AND METHODS

SNHG15 expression in 55 LC (lung cancer) tissues and 30 normal lung tissues was detected by qRT-PCR (quantitative Real Time-Polymerase Chain Reaction). The relationship between SNHG15 expression and pathological characteristics of LC patients was analyzed the by Kaplan-Meier method. The target microRNA of SNHG15 was predicted by bioinformatics and verified by dual-luciferase reporter gene assay. Viability, cell cycle and migration of LC cells after altering expressions of SNHG15 or microRNA-211-3p were detected by cell counting kit-8 (CCK-8), flow cytometry and transwell assay, respectively.

RESULTS

SNHG15 was highly expressed in LC tissues than that of normal lung tissues. Besides, LC patients with stage I-II presented lower expression of SNHG15 than those with stage III-IV. SNHG15 expression was correlated to tumor size, TNM stage, and lymph node metastasis, whereas not correlated to age and sex of LC patients. For in vitro studies, SNHG15 knockdown resulted in viability reduction, cell cycle arrest and reduced migration of LC cells, which were reversed by the microRNA-211-3p knockdown.

CONCLUSIONS

SNHG15 is highly expressed in LC tissues, which promotes the occurrence and progression of LC via regulating proliferation and migration of LC cells by targeting microRNA-211-3p.

摘要

目的

探讨长链非编码 RNA(lncRNA)SNHG15 是否可通过 microRNA-211-3p 调节肺癌的增殖和迁移,并探讨其潜在机制。

患者和方法

通过 qRT-PCR(实时定量聚合酶链反应)检测 55 例肺癌(LC)组织和 30 例正常肺组织中的 SNHG15 表达。采用 Kaplan-Meier 法分析 SNHG15 表达与 LC 患者病理特征的关系。通过生物信息学预测 SNHG15 的靶 microRNA,并通过双荧光素酶报告基因检测进行验证。通过细胞计数试剂盒-8(CCK-8)、流式细胞术和 Transwell 测定分别检测改变 SNHG15 或 microRNA-211-3p 表达后 LC 细胞的活力、细胞周期和迁移。

结果

SNHG15 在 LC 组织中的表达高于正常肺组织。此外,I-II 期 LC 患者的 SNHG15 表达低于 III-IV 期患者。SNHG15 表达与肿瘤大小、TNM 分期和淋巴结转移相关,而与 LC 患者的年龄和性别无关。在体外研究中,SNHG15 敲低导致 LC 细胞活力降低、细胞周期停滞和迁移减少,而 microRNA-211-3p 敲低可逆转这些变化。

结论

SNHG15 在 LC 组织中高表达,通过靶向 microRNA-211-3p 调节 LC 细胞的增殖和迁移,促进 LC 的发生和发展。

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