现代肿瘤医学
現代腫瘤醫學
현대종류의학
JOURNAL OF MODERN ONCOLOGY
2015年
17期
2410-2413
,共4页
周衍亮%党军强%任涛%胡昭华%朱政峰
週衍亮%黨軍彊%任濤%鬍昭華%硃政峰
주연량%당군강%임도%호소화%주정봉
肝癌%边缘群%肿瘤干细胞%microRNA
肝癌%邊緣群%腫瘤榦細胞%microRNA
간암%변연군%종류간세포%microRNA
liver cancer%side population%cancer stem cell%microRNA
目的:探讨转染miR-200a mimics对人肝癌细胞系MHCC97中边缘群细胞( SP)干细胞特性的影响。方法:利用流式细胞技术从MHCC97细胞中分离出SP细胞。转染组为应用脂质体介导转染miR-200a mimics的SP细胞,对照组为未接受转染的SP细胞。采用实时荧光定量RT-PCR检测两组SP细胞miR-200a的表达情况。四甲基偶氮唑盐( MTT)和软琼脂克隆形成实验检测细胞增殖情况。Transwell小室检测细胞迁移能力。裸鼠成瘤实验检测细胞体外成瘤能力。结果:转染miR-200a mimics可明显上调SP细胞miR
目的:探討轉染miR-200a mimics對人肝癌細胞繫MHCC97中邊緣群細胞( SP)榦細胞特性的影響。方法:利用流式細胞技術從MHCC97細胞中分離齣SP細胞。轉染組為應用脂質體介導轉染miR-200a mimics的SP細胞,對照組為未接受轉染的SP細胞。採用實時熒光定量RT-PCR檢測兩組SP細胞miR-200a的錶達情況。四甲基偶氮唑鹽( MTT)和軟瓊脂剋隆形成實驗檢測細胞增殖情況。Transwell小室檢測細胞遷移能力。裸鼠成瘤實驗檢測細胞體外成瘤能力。結果:轉染miR-200a mimics可明顯上調SP細胞miR
목적:탐토전염miR-200a mimics대인간암세포계MHCC97중변연군세포( SP)간세포특성적영향。방법:이용류식세포기술종MHCC97세포중분리출SP세포。전염조위응용지질체개도전염miR-200a mimics적SP세포,대조조위미접수전염적SP세포。채용실시형광정량RT-PCR검측량조SP세포miR-200a적표체정황。사갑기우담서염( MTT)화연경지극륭형성실험검측세포증식정황。Transwell소실검측세포천이능력。라서성류실험검측세포체외성류능력。결과:전염miR-200a mimics가명현상조SP세포miR
Objective:To investigatet the effects of miR-200a up-regulation on the characteristics of stem cells of side population in hepatocellular carcinoma cell line MHCC97. Methods:SP(side population)cells were isolated by fluorescence activated cell sorting( FACS)from MHCC97 cell line of human hepatocellular carcinoma. The miR-200a mimics was transfected into SP cells by liposome. The expression levels of miR-200a in SP cell pre- and post-tranfection was measured by reverse transcription polymerase chain reaction( RT-PCR ). MTT method and Soft agar cloning method was used to evalute the capability of cell proliferation. The invasion and migration capability of cells were evaluated by using transwell chamber model. Tumor cell implantation experiment was done to test the tu-morigenicity. Results:The expression of miR-200a in SP cell was obviously up-regulated transfection of post miR-200a mimics. MTT assay showed that the cell proliferation ability of SP in transfected group was obviously lower than control group(without transfection)(P<0. 05). The rate of clone formation was(24. 70 ± 5. 54)% in trans-fected group and it was(51. 63 ± 7. 11)% in control group(P<0. 05). Transwell chamber assay demonstrated the cell penetrating number was 18. 52 ± 4. 27 in transfected group and it was 63.34 ±7.41 in control group(P<0. 05). The number of tumors that formed in transfected group(1/8)was significantly lower than in the control group (8/8)(P<0. 05). Conclusion:Up-regulation of the miR-200a expression in SP cells of MHCC97 cell line would inhibit their ability of proliferation and migration,decrease their tumor formation ability in vitro,which is indicate the inhibition of the stem cell characteristics of SP cells.