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中华放射肿瘤学杂志
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中华放射肿瘤学杂志  2020, Vol. 29 Issue (7): 563-568    DOI: 10.3760/cma.j.cn113030-20190927-00399
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沉默lncRNA HOTTIP通过上调miR-663a表达增加非小细胞肺癌细胞系放射敏感性
魏少贤1, 牛锐1, 杨海林1, 李霞1, 王庆旭1, 刘俊2, 胡永强1
1河南省濮阳市油田总医院放疗科 457000;
2上海交通大学附属上海市胸科医院放疗科 200030
Silencing lncRNA HOTTIP affects radiosensitivity of non-small cell lung cancer cell lines by up-regulating miR-663a
Wei Shaoxian1, Niu Rui1, Yang Hailin1, Li Xia1, Wang Qingxu1, Liu Jun2,Hu Yongqiang1
1Department of Radiotherapy, Puyang Oilfield General Hospital of Henan Province, Puyang 457000, China;
2Department of Radiotherapy, Shanghai Chest Hospital Affiliated to Shanghai Jiaotong University, Shanghai 200030, China
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摘要 目的 探讨lncRNA HOTTIP通过调控miR-663a表达对4个非小细胞肺癌细胞系放射敏感性影响。方法 用0、2、4、6、8 Gy分别照射H838、H157、A549、H1299细胞系,采用克隆形成实验检测细胞存活情况。qRT-PCR检测细胞中HOTTIP和miR-663a表达水平。以A549、H1299细胞为研究对象,沉默HOTTIP表达、过表达miR-663a后用克隆形成实验检测细胞存活情况。流式细胞术检测细胞凋亡情况,Western blot检测Cleaved caspase-3、Cleaved PARP和γ-H2AX表达。双荧光素酶报告基因实验和qRT-PCR检测验证HOTTIP和miR-663a的靶向关系。结果 HOTTIP在放射耐受的H157、A549、H1299细胞中表达上调,miR-663a表达下调。沉默HOTTIP或过表达miR-663a均可抑制A549、H1299细胞存活(放射增敏比分别为1.562、1.507),促进Cleaved caspase-3、Cleaved PARP和γ-H2AX表达,促进放射照射诱导细胞凋亡。miR-663a是HOTTIP的靶基因,HOTTIP可负性调控miR-663a的表达。抑制miR-663a表达可逆转沉默HOTTIP对肺癌细胞系放射敏感性的影响。结论 沉默HOTTIP通过上调miR-663a表达,抑制肺癌细胞系存活,促进其凋亡,从而提高肺癌细胞系的放射敏感性。
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魏少贤
牛锐
杨海林
李霞
王庆旭
刘俊
胡永强
关键词 lncRNA HOTTIP基因miR-663a基因非小细胞肺癌细胞系放射敏感性    
AbstractObjective To investigate the effect of lncRNA HOTTIP on the radiosensitivity of four non-small cell lung cancer cell lines cultured in vitro by regulating the expression of miR-663a. Methods Four non-small cell lung cancer cell lines (H838, H157, A549, and H1299) were irradiated with different radiation intensities (0, 2, 4, 6, and 8 Gy). Cell survival was detected by colony formation assay. The expression levels of HOTTIP and miR-663a were detected by qRT-PCR. A549 and H1299 cells were selected for the subsequent experiment. After silencing HOTTIP and/or over-expressing miR-663a, cell survival was detected by colony formation assay. Cell apoptosis was detected by flow cytometry. The expression levels of Cleaved caspase-3, Cleaved PARP andγ-H2AX were quantitatively measured by Western blot. The targeting relationship between HOTTIP and miR-663a was vefiried by dual luciferase reporter assay and qRT-PCR. Results The expression of HOTTIP was up-regulated, whereas that of miR-663a was down-regulated in the radiation-resistant H157, A549 and H1299 cells. Silencing HOTTIP or over-expressing miR-663a inhibited the survival of A549 and H1299 cells (radiosensitization ratios were 1.562 and 1.507, respectively), promoted the expression of Cleaved caspase-3, Cleaved PARP and γ-H2AX, and accelerated cell apoptosis induced by radiation exposure. miR-663a was a target gene of HOTTIP, and HOTTIP negatively regulated the expression of miR-663a. The inhibition of miR-663a reversed the effect of silencing HOTTIP on the radiosensitivity of non-small cell lung cancer cells. Conclusion Silencing HOTTIP can suppress the survival of non-small cell lung cancer cells and promotes cell apoptosis by up-regulating the expression of miR-663a, thereby enhancing the radiosensitivity of non-small cell lung cancer cell lines.
Key wordslncRNA HOTTIP gene    miR-663a gene    Non-small cell lung cancer cell line    Radiosensitivity   
收稿日期: 2019-09-27     
通讯作者: 刘俊,Email:drjunliu@qq.com   
引用本文:   
魏少贤,牛锐,杨海林等. 沉默lncRNA HOTTIP通过上调miR-663a表达增加非小细胞肺癌细胞系放射敏感性[J]. 中华放射肿瘤学杂志, 2020, 29(7): 563-568.
Wei Shaoxian,Niu Rui,Yang Hailin et al. Silencing lncRNA HOTTIP affects radiosensitivity of non-small cell lung cancer cell lines by up-regulating miR-663a[J]. Chinese Journal of Radiation Oncology, 2020, 29(7): 563-568.
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http://journal12.magtechjournal.com/Jweb_fszlx/CN/10.3760/cma.j.cn113030-20190927-00399     或     http://journal12.magtechjournal.com/Jweb_fszlx/CN/Y2020/V29/I7/563
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