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miRNA-9对胃癌细胞增殖和迁移的作用研究 被引量:4

Study on the effect of miRNA-9 on the proliferation and migration of gastric cancer cells
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摘要 目的探讨微小RNA-9(miRNA-9)在胃癌细胞株中的表达及其对增殖和迁移的影响。方法运用脂质体转染法将miRNA-9类似物、miRNA-9抑制物和无关序列转染胃癌细胞MKN-45,记为miRNA-9类似物组、miRNA-9抑制物组、阴性对照组,以MKN-45细胞加新鲜的DMEM培养基作为空白对照组,荧光显微镜观察转染效率。转染48 h后,采用CCK-8检测细胞的增殖能力,Transwell小室检测细胞体外迁移行为。结果转染48 h后MKN-45细胞株转染效率达到90%。miRNA-9类似物促进细胞增殖;miRNA-9类似物转染组穿膜细胞数为(1052±71)个,miRNA-9抑制物组为(276±32)个,阴性对照组为(595±42)个,空白对照组为(613±35)个,miRNA-9类似物组穿膜细胞数较空白对照组、阴性对照组增多。结论miRNA-9在胃癌细胞中过表达,与胃癌细胞的恶性生物学行为密切相关。 Objective To investigate the expression of microRNA-9(miRNA-9)in gastric cancer cell lines and its effect on the proliferation and migration of cancer cells.Method The miRNA-9 analogs、miRNA-9 inhibitorsand irrelevent sequence plasmids were transiently transfected into gastric cancer cell lines MKN-45 using the liposome method.Thereafter,all cells were divided into four groups and three groups received plasmids were designated as the miRNA-9 analog group,miRNA-9 inhibitor group,negative control group and MKN-45 cells with fresh DMEM medium were selected as blank control group.The transfection efficiency was observed base on a fluorescence microscope.CCK-8 was used to detect cell proliferation,and Transwell chamber was used to detect the cell migration after 48 hours of transfection.Result The transfection efficiency of MKN-45 cell line was up to 90%at 48 hours of transfection,and miRNA-9 analogues remarkably promote cell proliferation.The count of transmembrane cells in the miRNA-9 analog group was(1052±71),the miRNA-9 inhibitor group was(276±32),the negative control group was(595±42),and the blank control group was(613±35).The number of transmembrane cells in the miRNA-9 analog group was higher than that of either the blank control group or the negative control group.Conclusion Overexpression of miRNA-9 in gastric cancer cells is closely related to the malignant biological behavior of gastric cancer cells.
作者 周建萍 余猛进 毛振彪 ZHOU Jianping;YU Mengjin;MAO Zhenbiao(Department of Emergency Medicine,the First Affiliated Hospital of the Second Military Medical University,Shanghai 200433,China;Department of Gastroenterology,Affiliated Hospital of Nantong University,Nantong 226001,Jiangsu,China)
出处 《癌症进展》 2020年第16期1637-1639,1671,共4页 Oncology Progress
关键词 miRNA-9 胃癌细胞 转染 增殖 迁移 miRNA-9 gastric cancer cells transfection proliferation migration
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  • 1Esteller M. Non-coding RNAs in human disease. Nat Rev Genet 2011; 12:861-74. 被引量:1
  • 2Bhatt K, Mi QS, Dong Z. microRNAs in kidneys: bio- genesis, regulation, and pathophysiological roles. Am J Physiol Renal Physio 2011; 300:F602-10. 被引量:1
  • 3Van Rooij E. The art of microRNA research. CircRes 2011; 108:219-34. 被引量:1
  • 4Lima RT, Busacca S, Almeida GM, et al. microRNA regulation of core apoptosis pathways in cancer. Eur J Cancer 2011; 47:163-74. 被引量:1
  • 5Davis-Dusenbery BN, Hata A. microRNA in Cancer: the involvement of aberrant microRNA biogenesis regula- tory Dathwavs. Genes Cancer 2010: 1:1100-14. 被引量:1
  • 6Farazi TA, Spitzer JI, Morozov P, Tuschi T. miRNAs in human cancer. J Patho12011; 223:102-15. 被引量:1
  • 7Fabian MR, Sonenberg N, Filipowicz W. Regulation of mRNA translation and stability by microRNAs. Annu Rev Biochem 2010; 79:351-79. 被引量:1
  • 8Lin SL, Chang DC, Ying SY, Leu D, Wu DT. micro- RNA miR-302 inhibits the tumorigenecity of humanpluripotent stem cells by coordinate suppression of the CDK2 and CDK4/6 cell cycle pathways. Cancer Res 2010; 70:9473-82. 被引量:1
  • 9Pickering MT, Stadler BM, Kowalik TF. miR-17 and miR-20a temper an E2Fl-induced G1 checkpoint to regulate cell cycle progression. Oncogene 2009; 28:140-5. 被引量:1
  • 10Pang RT, Leung CO, Ye TM, Liu M, Chiu PC, Lam KK. microRNA-34a suppresses invasion through downregu- lation of Notch1 and Jaggedl in cervical carcinoma and choriocarcinoma cells. Carcinogenesis 2010; 31: 1037- 44. 被引量:1

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