期刊文献+

miR-199a对膀胱癌抑制作用的研究 被引量:1

Inhibitory effect of miR-199a on bladder cancer
下载PDF
导出
摘要 目的研究miR-199a对膀胱癌的抑制作用。方法按处理方法不同将T24膀胱癌细胞分为空白对照组(control group)、pre-scamble转染组(pre-scamble group)、pre-miR-199a转染组(pre-miR-199a group)。采用MTT法检测转染miR-199a对细胞增殖的影响,用流式细胞仪检测转染miR-199a后对细胞凋亡及细胞周期的影响,Transwell侵袭实验检测细胞侵袭能力。结果 premiR-199a group OD值(0.436±0.042)显著低于control group(0.634±0.020)和pre-scamble group(0.601±0.059)(P<0.05)。premiR-199a group细胞凋亡率为(19.25±1.57)%,显著高于control group(10.19±0.98)%和pre-scamble group(12.27±1.38)%(P<0.05)。Control group、pre-scamble group和pre-miR-199a group的G1期细胞百分比分别为45.09%、47.57%、58.62%,转染pre-miR-199a使细胞停滞在G1期。pre-miR-199a group细胞透过滤膜的平均个数为(46.00±1.58)个,显著低于control group(67.00±1.58)个、pre-scamble group(61.20±1.30)个(P<0.05)。结论 miR-199a能抑制膀胱癌细胞的生长。 Objective To study the inhibitory effect of miR-199a on bladder cancer.Methods T24 bladder cancer cells were divided into control group, pre-scamble group and pre-miR-199a group according to different treatment.Cell proliferation was assayed by MTT, cell apoptosis and cell cycle by flow cytometry, and cell invasion by Transwell.ResuIts The OD value of pre-miR-199a group (0.436 ±0.042) was significantly lower than that of control group (0.634 ±0.020) and pre-scamble group (0.601 ±0.059)(P<0.05).Cell apoptosis of pre-miR-199a group(19.25 ±1.57)% was higher than that of control group(10.19 ±0.98)% and pre-scamble group(12.27 ±1.38)%(P<0.05).The cell ratio in G1 phase of control group、pre-scamble group and pre-miR-199a group was 45.09%, 47.57%, and 58.62%, respectively.The cell cycle arrested in G1 phase after transfected with pre-miR-199a.The cells migration number of pre-miR-199a group (46.00 ±1.58) was lower than those of control group(67.00 ±1.58) and pre-scamble group(61.20 ±1.30)(P<0.05).ConcIusion MiR-199a could inhibit the growth of bladder cancer cells.
出处 《中国生化药物杂志》 CAS 2015年第7期32-34,共3页 Chinese Journal of Biochemical Pharmaceutics
基金 卫计委吴阶平专项基金(320.6750.13216) 吉林省教育厅资助项目(吉教科合字[2014]第505号) 北华大学博士启动基因项目(2014)
关键词 miR-199a 膀胱癌 增殖 凋亡 细胞周期 侵袭 miR-199a bladder cancer proliferation apoptosis cell cycle migration
  • 相关文献

参考文献12

  • 1司彤.miR-199a在肾细胞癌中表达的临床意义及其对肾癌细胞生物学性状影响的实验研究[D]. 南方医科大学 2012
  • 2Martine Ploeg,Katja K. H. Aben,Lambertus A. Kiemeney.The present and future burden of urinary bladder cancer in the world[J]. World Journal of Urology . 2009 (3)
  • 3David P Bartel.MicroRNAs[J]. Cell . 2004 (2)
  • 4Lee Jeong-Won,Choi Chel Hun,Choi Jung-Joo,Park Young-Ae,Kim Seung-Jun,Hwang Seung Yong,Kim Woo Young,Kim Tae-Joong,Lee Je-Ho,Kim Byoung-Gie,Bae Duk-Soo.Altered MicroRNA expression in cervical carcinomas. Clinical cancer research : an official journal of the American Association for Cancer Research . 2008
  • 5Rodriguez Antony,Griffiths-Jones Sam,Ashurst Jennifer L,Bradley Allan.Identification of mammalian microRNA host genes and transcription units. Genome Research . 2004
  • 6Porkka Kati P,Pfeiffer Minja J,Waltering Kati K,Vessella Robert L,Tammela Teuvo L J,Visakorpi Tapio.MicroRNA expression profiling in prostate cancer. Cancer Research . 2007
  • 7Calin George A,Croce Carlo M.MicroRNA signatures in human cancers. Nature reviews. Cancer . 2006
  • 8Murakami Y,Yasuda T,Saigo K,Urashima T,Toyoda H,Okanoue T,Shimotohno K.Comprehensive analysis of microRNA expression patterns in hepatocellular carcinoma and non-tumorous tissues. Oncegene . 2005
  • 9Tao Yu,Xiao-yi Wang,Ren-guo Gong,An Li,Sen Yang,Yu-tang Cao,Yu-ming Wen,Chang-mei Wang,Xin-zhu Yi.The expression profile of microRNAs in a model of 7,12-dimethyl-benz[ a ]anthrance-induced oral carcinogenesis in Syrian hamster. Journal of Experimental & Clinical Cancer Research . 2009
  • 10Gebeshuber Christoph A,Zatloukal Kurt,Martinez Javier.miR-29a suppresses tristetraprolin, which is a regulator of epithelial polarity and metastasis. EMBO Reports . 2009

共引文献50

同被引文献7

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部