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Mithramycin A对肝癌细胞Huh-7增殖的影响 被引量:1

The effect of Mithramycin A on proliferation of human liver carcinoma cell line Huh-7
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摘要 目的研究抗肿瘤抗生素光辉霉素(Mithramycin A,MIT)对人肝癌细胞Huh-7的作用。方法CCK-8比色法观察MIT对Huh-7细胞的生长抑制作用,Hoechst 33342/PI双荧光染色分析细胞凋亡,流式细胞仪检测肿瘤细胞凋亡率。结果MIT可抑制Huh-7细胞的生长,半数抑制浓度(IC50)为60.12 nmol.L-1。荧光显微镜观察可见细胞凋亡特征性改变;浓度为5×10-2μmol.L-1的MIT作用72 h后,可明显诱导Huh-7细胞凋亡,流式细胞仪检测肿瘤细胞出现典型亚二倍体凋亡小峰。结论MIT对Huh-7细胞有明显的诱导凋亡和生长抑制作用,具有浓度、时间依赖性。 Objective To examine the effect of Mithramycin A (MIT) on the human liver tumour cell line Huh-7. Methods Huh-7 cells were treated with MIT at different concentrations, and the inhibitory effect on cell growth was analyzed by CCK-8 colorimetric assay and the cells were observed under fluorescent microscope for cell apoptosis by using Hoechst33342/PI double fluorescent staining approach. The effect of MIT on the apoptotic rate of tumour cells was analyzed by flow cytometry. Results The treatment of Huh-7 cells with MIT inhibited cell growth and IC50 value of MIT for Huh-7 cells was 60. 12 μmol.L^-1. The characteristic signs of apoptosis were observed under a fluorescent microscope, and apoptosis of Huh-7 cells can be induced by MIT at concentration of 5 × 10^-2μmol.L^- 1 in 72 h. After 72 h treatment with MIT, some apoptotic cells were detected and a typical subdiploid peak was observed by flow cytometry. Conclusion MIT can efficiently induce apoptosis of Huh-7 cells and inhibit the cell growth in a dose-dependent and timedependent manet
出处 《同济大学学报(医学版)》 CAS 2009年第5期32-35,39,共5页 Journal of Tongji University(Medical Science)
基金 上海市浦江人才计划资助项目(06PJ14096) 上海市科委资助项目(054119628)
关键词 HUH-7细胞 光辉霉素A 凋亡 Huh-7 cell Mithramycin A apoptosis
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  • 1I. Leroy,G. Laurent,A. Quillet-Mary. Mithramycin A activates Fas death pathway in leukemic cell lines[J] 2006,Apoptosis(1):113~119

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  • 1Sonia AM,Manel E. Dysregulation of microRNAs in cancer:Playing with fire[J].FEBS Letters,2010,(13):2087-2099.
  • 2Babashah S,Soleimani M. The oncogenic and tumour suppressive roles of microRNAs in cancer and apoptosis[J].European Journal of Cancer,2011,(08):1127-1137.
  • 3Aigner A. MicroRNAs (miRNAs) in cancer invasion and metastasis:therapeutic approaches based on metastasis-related miRNAs[J].J Mol Med (Berl),2011,(05):445-457.
  • 4Dillhoff M,Wojcik SE,Bloomston M. MicroRNAs in solid tumors[J].Journal of Surgical Research,2009,(02):349-354.
  • 5Furuta M,Kozaki KI,Tanaka S. miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma[J].Carcinogenesis,2010,(05):766-776.
  • 6Shimizu S,Takehara T,Hikita H. The let-7 family of microRNAs inhibits Bcl-xL expression and potentiates sorafenib-induced apoptosis in human hepatocellular carcinoma[J].Journal of Hepatology,2011,(05):698-704.
  • 7Budhu A,Jia HL,Forgues M. Identification of metastasis-related microRNAs in hepatocellular carcinoma[J].Hepatology,2008,(03):897-907.
  • 8Li R,Qian NS,Tao KS. MicroRNAs involved in neoplastic transformation of liver cancer stem cells[J].Journal of Experimental & Clinical Cancer Research,2010.169.
  • 9Xu JA,Wu C,Che X. Circulating microRNAs,miR-21,miR-122,and miR-223,in patients with hepatocellular carcinoma or chronic hepatitis[J].Molecular Carcinogenesis,2011,(02):136-142.
  • 10Qu KZ,Zhang K,Li HR. Circulating microRNAs as biomarkers for hepatocellular carcinoma[J].Journal of Clinical Gastroenterology,2011,(04):355-360.

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