MicroRNA-1304 suppresses human non-small cell lung cancer cell growth in vitro by targeting heme oxygenase-1
Li, Cheng-gang1,2; Pu, Meng-fan1,2; Li, Chun-zhu1,2; Gao, Man1,2; Liu, Ming-xia1,2; Yu, Cun-zhi1,2; Yan, Hong1,2; Peng, Chun1,2; Zhao, Yang1,2; Li, Yu1,2
刊名ACTA PHARMACOLOGICA SINICA
2017-01
卷号38期号:1页码:110-119
关键词miR-1304 NSCLC heme oxygenase-1 hemin
ISSN号1671-4083
DOI10.1038/aps.2016.92
文献子类Article
英文摘要Previous studies have shown that microRNA-1304 (miR-1304) is dysregulated in certain types of cancers, including non-small cell lung cancer (NSCLC), and might be involved in tumor survival and/or growth. In this study we investigated the direct target of miR-1304 and its function in NSCLC in vitro. Human lung adenocarcinoma cell lines (A549 and NCI-H1975) were studied. The cell proliferation and survival were investigated via cell counting, MTT and colony-formation assays. Cell apoptosis and cell cycle were examined using annexin V-PE/7-AAD and PI staining assays, respectively. The dual-luciferase reporter assay was used to verify post-transcriptional regulation of heme oxygenase-1 (HO-1) by miR-1304. CRISPR/Cas9 was used to deplete endogenous miR-1304. Overexpression of MiR-1304 significantly decreased the number and viability of NSCLC cells and colony formation, and induced cell apoptosis and G(0)/G(1) phase cell cycle arrest. HO-1 was demonstrated to be a direct target of miR-1304 in NSCLC cells. Restoration of HO-1 expression by hemin (20 mu mol/L) abolished the inhibition of miR-1304 on cell growth and rescued miR-1304-induced apoptosis in A549 cells. Suppression of endogenous miR-1304 with anti-1304 significantly increased HO-1 expression and promoted cell growth and survival in A549 cells. In 17 human NSCLC tissue samples, miR-1304 expression was significantly decreased, while HO-1 expression was significantly increased as compared to normal lung tissues. MicroRNA-1304 is a tumor suppressor and HO-1 is its direct target in NSCLC. The results suggest the potential for miR-1304 as a therapeutic target for NSCLC.
资助项目National Science and Technology Major Project[2012ZX09302-003] ; National Science and Technology Major Project[2012ZX09301-001-006] ; National Science and Technology Major Project[2015ZX09102005]
WOS关键词BREAST-CANCER ; PROLIFERATION ; EXPRESSION ; PATHWAY ; HO-1 ; TRANSLATION ; METASTASIS ; INHIBITION ; CARCINOMA ; APOPTOSIS
WOS研究方向Chemistry ; Pharmacology & Pharmacy
语种英语
CSCD记录号CSCD:5906822
出版者ACTA PHARMACOLOGICA SINICA
WOS记录号WOS:000393540900010
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/275741]  
专题药物安全性评价中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Miao, Ling-ling; Ren, Jin
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Ctr Drug Safety Evaluat & Res, Shanghai 201203, Peoples R China;
2.Univ Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Ctr Drug Safety Evaluat & Res, Beijing 100049, Peoples R China;
3.Beijing Inst Basic Med Sci, Brain Sci Ctr, Beijing 100850, Peoples R China
推荐引用方式
GB/T 7714
Li, Cheng-gang,Pu, Meng-fan,Li, Chun-zhu,et al. MicroRNA-1304 suppresses human non-small cell lung cancer cell growth in vitro by targeting heme oxygenase-1[J]. ACTA PHARMACOLOGICA SINICA,2017,38(1):110-119.
APA Li, Cheng-gang.,Pu, Meng-fan.,Li, Chun-zhu.,Gao, Man.,Liu, Ming-xia.,...&Ren, Jin.(2017).MicroRNA-1304 suppresses human non-small cell lung cancer cell growth in vitro by targeting heme oxygenase-1.ACTA PHARMACOLOGICA SINICA,38(1),110-119.
MLA Li, Cheng-gang,et al."MicroRNA-1304 suppresses human non-small cell lung cancer cell growth in vitro by targeting heme oxygenase-1".ACTA PHARMACOLOGICA SINICA 38.1(2017):110-119.
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