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作 者:喻超[1] 江建新[1] 黎志鹏[1] 肖杰[1] 潘耀振[1] 孙诚谊[1]
机构地区:[1]贵州医科大学附院肝胆外科,贵州贵阳550004
出 处:《贵阳医学院学报》2015年第8期793-796,800,共5页Journal of Guiyang Medical College
基 金:国家自然科学基金(No.81160311);国家国际科技合作专项(No.2014DFA31420);贵阳市科技计划项目[筑科合同(20141001)46号];贵州省科学技术基金[黔科合J字(2015)2013号]
摘 要:目的:研究microRNA-100(miR-100)对人胰腺癌细胞MIA Pa Ca-2和CFPAC-1增殖及皮下成瘤能力的影响。方法:用miR-100慢病毒过表达载体感染MIA Pa Ca-2和CFPAC-1细胞,构建高表达miR-100细胞株;用平板克隆、CCK-8方法检测miR-100对人胰腺癌细胞体外增殖能力,裸鼠皮下成瘤实验检测miR-100对人胰腺癌细胞成瘤能力。结果:慢病毒感染后,miR-100表达在MIA Pa Ca-2细胞中提高(941±171)倍,在CFPAC-1细胞中提高(154±23)倍,差异有统计学意义(P<0.05);平板克隆形成实验提示MIA Pa Ca-2和CFPAC-1细胞实验组平板克隆数少于对照组病毒,差异有统计学意义(P<0.05);CCK-8细胞增殖实验提示MIA Pa Ca-2和CFPAC-1细胞实验组增殖能力弱于对照组,差异有统计学意义(P<0.05);裸鼠皮下成瘤实验显示,miR-100抑制了肿瘤裸鼠皮下成瘤。结论:miR-100能从体内外抑制人胰腺癌细胞增殖及皮下成瘤能力。Objective:To investigate the effects of miR-100 on proliferation and tumorigenicity of MIA PaCa-2 and CFPAC-1 cells. Methods:Using miR-100 lentivirus overexpression vector to infect MIA PaCa-2 and CFPAC-1 cells to establish miR-100 cell strain. Pancreatic cancer cell proliferation was analyzed using CCK-8 and colony formation assay. BALB/c Nude mice subcutaneous tumor exper-iment was adopted to test the effect of micorRNA-100 on HPCC. Results:The expression of miR-100 after infected by miR-100 lentivirus was(941 ± 171)folds in MIA PaCa-2 cells,and(154 ± 23)folds in CFPAC-1 cells,the differences were statistically significant(P ﹤0. 05). Colony formation assay prompted the number of clones of MIA PaCa-2 and CFPAC-1 cells in experimental group were less than the control group,the difference was statistically significant(P﹤0. 05);CCK-8 cell proliferation ex-periments suggested that MIA PaCa-2 and CFPAC-1 cell proliferation in the experimental group was weaker than that of control group,difference was statistically significant(P﹤0. 05). Nude mice sub-cutaneous tumor experiment suggested that miR-100 inhibited tumor growth. Conclusions:miR-100 can inhibit human pancreatic cancer cell proliferation and tumorigenicity.
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