期刊文献+

不同转移潜能食管癌细胞株裸鼠模型的建立 被引量:5

Establishment of Esophageal Cancer Cell Lines with Different Metastatic Potential in Nude Mice Model
暂未订购
导出
摘要 背景:食管癌的转移率较高,是导致患者死亡的主要原因,但其机制仍不完全清楚。目的:建立具有不同转移潜能的高侵袭能力食管癌细胞株亚系裸鼠模型。方法:应用Transwell侵袭小室从食管癌细胞株Eca-109中筛选出高侵袭能力的食管癌细胞株亚系。观察母系和亚系细胞形态,MTT法检测细胞增殖能力的变化,划痕法检测细胞迁移能力。将食管癌Eca-109细胞及其亚系Eca-109 T4细胞分别皮下注射于裸鼠体内诱导移植瘤模型,观察成瘤率、成瘤时间、肿瘤生长情况。结果:成功从食管癌Eca-109细胞株中筛选出高侵袭能力的食管癌细胞株亚系Eca-109 T4,两者细胞形态无明显差异。与Eca-109细胞相比,Eca-109 T4细胞增殖能力和划痕愈合能力均明显增强。Eca-109组和Eca-109 T4组裸鼠成瘤率均为100%,与Eca-109组相比,Eca-109 T4组裸鼠成瘤时间更早且瘤体生长更快。结论:成功建立了不同转移潜能的高侵袭能力食管癌细胞株亚系裸鼠成瘤模型,为食管癌转移的进一步研究提供了理想模型。 Background: Esophageal cancer has a high metastasis rate, which is the main cause of death, but its mechanism is not completely clear yet. Aims: To establish an esophageal cancer cell subline with a metastatic potential of high invasion capacity in nude mice. Methods: Transwell invasion chamber was used to subdivide esophageal cancer cell subline from esophageal cancer cell line Eca-109. The cell morphology of parent line and subline was examined. MTT method was used to detect changes of cell proliferation. Cell migration was determined by scratch method. Esophageal cancer Eca-109 cells and its subline Eca-109 T4 cells were subcutaneously injected into nude mice to induce transplantation model, respectively. Tumor formation rate, time for tumor formation, and tumor growth in nude mice were observed. Results: Esophageal cancer cell subline Eca-109 T4 was successfully established. No significant difference in cell morphology was found between Eca-109 cells and Eca-109 T4 cells. Capacities of cell proliferation and migration in Eca-109 T4 cells were significantly higher when compared with Eca-109 cells. Tumor formation rate in nude mice injected with Eca-109 and Eca-109 T4 cells were 100%, time for tumor formation was earlier in Eca-109 T4 nude mice than in Eca-109 nude mice, and tumor growth was significantly increased. Conclusions: An esophageal cancer cell subline with a metastatic potential of high invasion capacity in nude mice was successfully established, which provides an ideal model for the further study of esophageal cancer metastasis.
出处 《胃肠病学》 2013年第9期548-551,共4页 Chinese Journal of Gastroenterology
基金 新疆维吾尔自治区自然科学基金(2010211B20)资助
关键词 食管肿瘤 细胞系 肿瘤 小鼠 肿瘤转移 Esophageal Neoplasms Cell Line, Tumor Mice, Nude Neoplasm Metastasis
  • 相关文献

参考文献1

  • 1Jun Hui Cui~1 Uwe Krueger~2 Doris Henne-Bruns~2 Bemd Kremer~2 Holger Kalthoff~2 ~1Department of General Surgery,First Affiliated Hospital,College of Medicine,Zhejiang University,Hangzhou 310003,Zhejiang Province,China ~2Department of General Surgery,Christian-Albrechts-University,Kiel,GermanyDr.Jun Hui Cui graduated from Zhejiang Medical University in 1984,earned master degree in 1990,studied in the Surgical Department of Kiel University and worked in the Lab of Molecular Oncology of Kiel University from 1994-1997achieved M.D.from Kiel University.Germany,now associate professor of surgery,specialized in colorectal oncology.Adviser of graduated student for master degree,having 20 publications published in key Chinese or English journals..Orthotopic transplantation model of human gastrointestinal cancer and detection of micrometastases[J].World Journal of Gastroenterology,2001,7(3):381-386. 被引量:19

二级参考文献1

共引文献18

同被引文献36

  • 1张凌志,邸菁,王运杰,赵昕,张朝东.Transwell小室筛选高侵袭性C6细胞MMP-2和TIMP-2的表达[J].肿瘤防治杂志,2005,12(10):742-745. 被引量:6
  • 2UMAR S B,FLEISCHER D E.Esophageal cancer:epidemiology,pathogenesis and prevention[J].Nat Clin Pract Gastroenterol Hepatol,2008,5(9):517-526.
  • 3LIU K S,ZHANG Y,DING W C,et al.The selective Hsp90 inhibitor BJ-B11 exhibits potent antitumor ac tivity via induction of cell cycle arrest,apoptosis and autophagy in Eca-109 human esophageal squamous carcinoma cells[J].Int J Oncol,2012,41(6):2276-2284.
  • 4AGUILA M,BEVILACQUA D,MCCULLEY C,et al.Hsp90 inhibition protects against inherited retinal degeneration[J].Human Molecular Genetics,2014,23(8):2164-2175.
  • 5CHEN Y K,CHANG W S,WU I C,et al.Molecular characterization of invasive subpopulations from an esophageal squamous cell carcinoma cell line[J].Anticancer Res,2010,30(3):727-736.
  • 6IMAKAWA K.Real time PCR:principle and usage[J].Tanpakushitsu Kakusan Koso,2004,49 (11 Suppl):1476-1483.
  • 7SCHNEIDER R,LINKA R M,REINKE H.HSP90 Affects the stability of BMAL1 and circadian gene expression[J].J Biological Rhythms,2014,29 (2):87-96.
  • 8NAGARAJU G P,LONG T E,PARK W,et al.Heat shock protein 90 promotes epithelial to mesenchymal transition,invasion,and migration in colorectal cancer[J].Mol Carcinog,2014[Epub ahead of print].
  • 9IMAI T,KATO Y,KAJIWARA C,et al.Heat shock protein 90 (HSP90) contributes to cytosolic transloca tion of extracellular antigen for cross-presentation by dendritic cells[J].Proc Natl Acad Sci U S A,2011,108(39):16363-16368.
  • 10BRADLEY E,BIEBERICH E,MIVECHI N F,et al.Regulation of embryonic stem cell pluripotency by heat shock protein 90[J].Stem Cells,2012,30(8):1624-1633.

引证文献5

二级引证文献10

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