科研成果详情

题名miR-138 suppresses the proliferation, metastasis and autophagy of non-small cell lung cancer by targeting Sirt1
作者
发表日期2017-06
发表期刊ONCOLOGY REPORTS   影响因子和分区
语种英语
原始文献类型Article
关键词miR-138 non-small cell lung cancer autophagy mTOR signaling pathway
其他关键词EPITHELIAL-MESENCHYMAL TRANSITION ; AMPK/MTOR PATHWAY ; TUMOR-SUPPRESSOR ; CERVICAL-CANCER ; GASTRIC-CANCER ; UP-REGULATION ; DEACETYLASE ; PROMOTES ; SURVIVAL ; PROTEIN
摘要The present study determined the role and mechanism of miR-138 in non-small cell lung cancer (NSCLC). In total, 45 freshly resected clinical NSCLC tissues were collected. The expression of miR-138 in tissues and cell lines were determined by real-time quantitative PCR. miR-138 mimics were transfected into A549 and Calu-3 cells in vitro, and then the effects of miR-138 on lung cancer cell proliferation, cell cycle, invasion and metastasis were investigated by CCK-8 assay, Transwell and flow cytometry, respectively. The protein expression of the potential target gene Sirt1 in lung cancer cells were determined by western blot analysis. Dual-Luciferase reporter assay was performed to further confirm whether Sirt1 was the target gene of miR-138. The expression of miR-138 was significantly lower in lung cancer tissues and was negatively correlated to the differentiation degree and lymph node metastasis of lung cancer. In vitro experiment results showed that miR-138 inhibited lung cancer cell proliferation, invasion and migration. It was verified that miR-138 could downregulate Sirtl protein expression, inhibit epithelial-mesenchymal transition (EMT), decrease the activity of AMPK signaling pathway and elevate mTOR phosphorylation level. Dual-Luciferase reporter assay demonstrated that miR-138 could directly regulate Sirt1. Downregulation of Sirtl alone can also cause the same molecular and biological function changes. Western blot analysis and confocal microscopy results indicated that overexpression of miR-138 or interference of Sirtl expression could inhibit lung cancer cell autophagy activity possibly through AMPK-mTOR signaling pathway. miR-138 plays a tumor suppressor function in lung cancer. It may inhibit the proliferation, invasion and migration of lung cancer through downregulation of Sirtl expression and activation of cell autophagy. The downregulation of miR-138 is closely related to the development of lung cancer.
资助项目Program of Science Technology Department of Zhejiang Province [2016C33SAB0009]; Program of Science and Technology Bureau of Lishui City [2014JYZB12]
出版者SPANDIDOS PUBL LTD
出版地ATHENS
ISSN1021-335X
EISSN1791-2431
卷号37期号:6页码:3244-3252
DOI10.3892/or.2017.5619
页数9
WOS类目Oncology
WOS研究方向Oncology
WOS记录号WOS:000402692300011
收录类别SCIE ; PUBMED ; SCOPUS
URL查看原文
PubMed ID28498463
PMC记录号PMC5442395
SCOPUSEID2-s2.0-85019559304
通讯作者地址[Lou, Tianzheng]Sixth Affiliated Hospital of Wenzhou Medical University,Lishui People's Hospitlal,Lishui, Zhejiang,323000,China
Scopus学科分类Oncology;Cancer Research
引用统计
被引频次:44[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/16021
专题其他_附属第六医院(丽水市人民医院)
附属第一医院
第二临床医学院,附属第二医院、育英儿童医院_麻醉学_ICU
通讯作者Lou, Tianzheng
作者单位
1.Sixth Affiliated Hospital of Wenzhou Medical University,Lishui People's Hospitlal,Lishui, Zhejiang,323000,China;
2.Central Hospital of Lishui City,Lishui, Zhejiang,323000,China;
3.First Affiliated Hospital of Wenzhou Medical University,Lishui, Zhejiang,323000,China;
4.Department of ICU,Sixth Affiliated Hospital of Wenzhou Medical University,Lishui People's Hospital,Lishui, Zhejiang,323000,China
第一作者单位温州医科大学
通讯作者单位温州医科大学
第一作者的第一单位温州医科大学
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Ye, Zaiting,Fang, Bingmu,Pan, Jiongwei,et al. miR-138 suppresses the proliferation, metastasis and autophagy of non-small cell lung cancer by targeting Sirt1[J]. ONCOLOGY REPORTS,2017,37(6):3244-3252.
APA Ye, Zaiting., Fang, Bingmu., Pan, Jiongwei., Zhang, Ning., Huang, Jinwei., ... & Cao, Zhuo. (2017). miR-138 suppresses the proliferation, metastasis and autophagy of non-small cell lung cancer by targeting Sirt1. ONCOLOGY REPORTS, 37(6), 3244-3252.
MLA Ye, Zaiting,et al."miR-138 suppresses the proliferation, metastasis and autophagy of non-small cell lung cancer by targeting Sirt1".ONCOLOGY REPORTS 37.6(2017):3244-3252.

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