miR-142-3p靶向FSTL1基因对结直肠癌细胞增殖、凋亡以及放疗敏感性的影响  被引量:1

Effect of microRNA-142-3p regulation the proliferation, apoptosis and radiosensitivity by targeting FSTL1 in colorectal cancer cells

在线阅读下载全文

作  者:董明强 汪蕊[1] 王志华[1] 江炳东[1] Dong Mingqiang;Wang Rui;Wang Zhihua;Jiang Bingdong(Department of Oncology,First People's Hospital of Jingmen City,Hubei Province,Jingmen 448000,China)

机构地区:[1]湖北省荆门市第一人民医院肿瘤科

出  处:《中华细胞与干细胞杂志(电子版)》2019年第4期216-223,共8页Chinese Journal of Cell and Stem Cell(Electronic Edition)

摘  要:目的探究miR-142-3p靶向卵泡抑素样蛋白1(FSTL1)对结直肠癌(CRC)细胞增殖、凋亡以及放疗敏感性的影响。方法培养正常人结肠细胞FHC与CRC细胞系SW480、DLD-1、HCT116和Caco-2,qRT-PCR检测细胞中miR-142-3P水平,WesternBlot检测FSTL1蛋白水平;分别转染miR-142-3p模拟物(miR-142-3p组)、模拟物阴性对照(miR-NC组)、FSTL1的si-RNA9(si-FSTL1组)、si-RNA阴性对照(si-con组)至CRCSW480细胞,MTT检测细胞增殖情况,流式细胞仪检测细胞凋亡水平,WesternBlot检测增殖、凋亡相关蛋白水平,克隆形成实验检测放射敏感性;双荧光素酶报告基因、WesternBlot验证miR-142-3p与FSTL1关系及在CRC中作用。采用t检验和方差分析进行统计学分析。结果CRC细胞SW480、DLD-1、HCT116、Caco-2中miR-142-3p水平(0.86±0.09、1.09±0.11、0.76±0.08、0.98±0.10)低于正常结肠细胞FHC(2.56±0.26),差异具有统计学意义(t=18.536,15.621,19.851,17.016,P均<0.01),FSTL1mRNA水平2.26±0.23、1.39±0.14、2.01±0.20、1.98±0.19高于FHC细胞(0.79±0.08),差异具有统计学意义(t=18.110,11.163,16.991,17.317,P均<0.01),FSTL1蛋白水平(1.16±0.12、1.09±0.11、0.96±0.09、0.95±0.10)高于FHC细胞(0.37±0.04),差异有统计学意义(t=18.736,18.454,17.972,16.155,P均<0.01);miR-142-3p组CRC细胞SW480凋亡率(30.23±3.10)和Bax水平(1.02±0.11)高于miR-con组8.96±0.89,0.45±0.05,t=19.785,14.152,P均<0.01,72h细胞增殖活力(1.16±0.11)、CyclinD1(0.35±0.05)、Bcl-2(0.38±0.04)、8Gy(7.56±0.75)细胞存活率低于miR-con组(1.60±0.16,1.02±0.12,0.98±0.10,10.35±1.25,t=6.798,15.462,16.713,5.742,P均<0.01);si-FSTL1组SW480细胞72h的细胞增殖活力(1.05±0.11)、CyclinD1(0.40±0.05)、Bcl-2(0.42±0.05)低于si-con组(1.60±0.16,1.05±0.10,1.00±0.12,t=8.498,17.441,13.385,P均<0.01),Bax(1.00±0.11)高于si-con组(0.41±0.04,t=15.122,P<0.01);miR-142-3p负调控FSTL1表达,过表达FSTL1逆转了miR-142-3p过表达SW480细胞增殖、凋亡及放射敏感性的影响。结论过表达miR-142-3p可�Objective To investigate the effects of microRNA-142-3p targeting follistatin-like protein 1 on proliferation,apoptosis and radiosensitivity of colorectal cancer cells.Methods The normal human colon cell FHC and CRC cell lines SW480,DLD-1,HCT116 and Caco-2 were cultured,the level of miR-142-3P was detected by qRT-PCR,and the level of FSTL1 protein was detected by Western Blot.MiR-142-3p mimics(miR-142-3p group),mimics negative control(miR-NC group),si-RNA of FSTL1(si-FSTL1 group),si-RNA negative control(si-con group)were transfected into CRC SW480 cells,respectively.MTT was used to detect cell proliferation,flow cytometry was used to detect cell apoptosis,Western Blot was used to detect the levels of proliferation and apoptosis-related proteins,and cloning formation assay was used to detect radiosensitivity.Luciferase and Western Blot were used to verify the relationship between microRNA-142-3p and FSTL1 and its role in colorectal cancer.Statistical analysis was performed using t test and analysis of variance.Results The levels of miR-142-3p in colorectal cancer cells SW480,DLD-1,HCT116,and Caco-2(0.86±0.09,1.09±0.11,0.76±0.08,0.98±0.10)were lower than those of normal Colonic cells FHC(2.56±0.26,t=18.536,15.621,19.851,17.016,P<0.01),FSTL1 mRNA levels(2.26±0.23,1.39±0.14,2.01±0.20,1.98±0.19)were higher than FHC cell levels(0.79±0.08,t=18.110,11.163,16.991,17.317,P<0.01),and FSTL1 protein levels(1.16±0.12,1.09±0.11,0.96±0.09,0.95±0.10)were higher than FHC cell levels(0.37±0.04,t=18.736,18.454,17.972,16.155,P<0.01);the apoptosis rate of colorectal cancer cell SW480 in miR-142-3p group(30.23±3.10)and Bax level(1.02±0.11)were higher than that in miR-con group(8.96±0.89,t=19.785,P<0.01;0.45±0.05,t=14.152,P<0.01),and cell proliferation activity for 72 h(1.16±0.11),the levels of CyclinD1(0.35±0.05)and Bcl-2(0.38±0.04),and the cell survival rate after 8 Gy were lower than that of the miR-con group(1.60±0.16,t=6.798,P<0.01;1.02±0.12,t=15.462,P<0.01;0.98±0.10,t=16.713,P<0.01;10.35±1.25,t=5.742,P<0.

关 键 词:miR-142-3p 卵泡抑素样蛋白1 结直肠癌 增殖 凋亡 放疗敏感性 

分 类 号:R735.3[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象