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 |
DOI | 10.1038/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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