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微小RNA-1260b通过靶向蛋白酪氨酸磷酸酶受体K促进非小细胞肺癌的迁移和侵袭。

MiR-1260b promotes the migration and invasion in non-small cell lung cancer via targeting PTPRK.

作者信息

Xu Limin, Xu Xuting, Huang Huilian, Ma Zhihong, Zhang Shuangmei, Niu Pingping, Chen Yingrong, Ping Jinliang, Lu Ping, Yu Caihua, Min Lishan, Chen Jing, Dai Licheng, Dong Shunli

机构信息

Huzhou Key Laboratory of Molecular Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.

Respiratory Medicine, Huzhou Central Hospital, Huzhou, Zhejiang, 313000, China.

出版信息

Pathol Res Pract. 2018 May;214(5):776-783. doi: 10.1016/j.prp.2018.02.002. Epub 2018 Feb 14.

Abstract

OBJECTIVE

Non-small cell lung cancer (NSCLC) accounts for 80-85% of lung cancer cases which cause most of cancer-related deaths globally. As our previous study discovered miR-1260b can be regarded as a specific signature for metastasis in NSCLC patients. However, the molecular mechanisms of miR-1260b underlying NSCLC progression and metastasis remain dismal.

METHODS

The expression of miR-1260b in NSCLC tissues and cell lines were examined by real-time PCR, the effects of miR-1260b on cell migration, invasion and proliferation were evaluated in vitro. Furthermore, luciferase reporter assay was performed to identify the targets of miR-1260b, and the association between miR-1260b and its target gene was determined by real-time PCR and western blot assay.

RESULTS

The results showed that miR-1260b was significantly upregulated in NSCLC cell lines. The inhibition of miR-1260b expression decreased the migratory and invasive rates in A549 cells while miR-1260b overexpression had the opposite effect. Furthermore, PTPRK was identified as a direct target of miR-1260b, and PTPRK expression was inversely correlated with miR-1260b in NSCLC cell lines and clinical tissues.

CONCLUSIONS

These results suggested that miR-1260b may play an important role in NSCLC metastasis progression and could serve as a putative target for diagnosis and treatment of NSCLC.

摘要

目的

非小细胞肺癌(NSCLC)占肺癌病例的80 - 85%,在全球范围内导致了大部分癌症相关死亡。正如我们之前的研究发现,miR - 1260b可被视为NSCLC患者转移的一个特定标志物。然而,miR - 1260b在NSCLC进展和转移中的分子机制仍不清楚。

方法

通过实时定量PCR检测miR - 1260b在NSCLC组织和细胞系中的表达,在体外评估miR - 1260b对细胞迁移、侵袭和增殖的影响。此外,进行荧光素酶报告基因检测以鉴定miR - 1260b的靶标,并通过实时定量PCR和蛋白质免疫印迹法确定miR - 1260b与其靶基因之间的关联。

结果

结果显示,miR - 1260b在NSCLC细胞系中显著上调。抑制miR - 1260b表达可降低A549细胞的迁移和侵袭率,而miR - 1260b过表达则有相反的效果。此外,PTPRK被鉴定为miR - 1260b的直接靶标,在NSCLC细胞系和临床组织中,PTPRK表达与miR - 1260b呈负相关。

结论

这些结果表明,miR - 1260b可能在NSCLC转移进展中起重要作用,并可作为NSCLC诊断和治疗的一个潜在靶点。

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