期刊文献+

外源性FHIT基因对人乳腺癌MDA-MB-436细胞恶性表型的影响

Effects of exogenous FHIT gene on malignant phenotype of human breast cancer cell line MDA-MB-436
原文传递
导出
摘要 目的:研究外源性脆性组氨酸三联体(FHIT)基因的表达对乳腺癌MDA-MB-436细胞增殖的影响并探讨其机制。方法:通过脂质体将外源性FHIT基因的真核表达质粒PEGFP-FHIT和空载体分别转染FHIT表达缺失的乳腺癌细胞MDA-MB-436。MTT法分析细胞增殖,流式细胞术观察细胞的凋亡,蛋白质印迹法检测外源性FHIT基因及凋亡相关基因Caspase-3、-8、-9的蛋白表达。结果:PEGFP-FHIT组细胞的生长抑制率和凋亡率明显高于空载体组和对照组,PEGFP-FHIT组细胞Caspase-3、-9活性片段表达上调。结论:外源性FHIT基因表达能抑制MDA-MB-436细胞增殖,其机制可能是通过激活Caspase途径从而诱导细胞凋亡。 OBJECTIVE: To investigate the effects of the FHIT gene on the malignant growth of breast cancer cell line MDA-MB-436 and its mechanism of cancer inhibition.METHODSD: Mammaliam expression vector PEGFP-FHIT was transfected into the breast cancer cell line MDA-MB-436 by liprofectamine.The effect of FHIT on the growth of MDA-MB-436 was examined by MTT and flow cytometry.The expressions of exogenous FHIT protein and Caspase-3,-8,-9 were detected by Western blot.RESULTS: The growth inhibitory rate and apoptosis rate of the cells in PEGFP-FHIT group were significantly higher than those in the PEGFP group and control group.The expressions of caspase-3,-9 active proteins were significant increased in the PEGFP-FHIT group.CONCLUSION:The expressions of exogenous FHIT gene can obviously suppress the proliferation and induce apoptosis by the activation of the caspase pathway in MDA-MB-436 cells.
出处 《中华肿瘤防治杂志》 CAS 2010年第13期979-981,共3页 Chinese Journal of Cancer Prevention and Treatment
基金 广东省卫生厅科研项目(B2007143)
关键词 脆性组氨酸三联体基因 乳腺肿瘤 基因转染 细胞凋亡 fragile histidine triad gene breast neoplasms gene transfection apoptosis
  • 相关文献

参考文献10

  • 1Gulnur G, Aysegul U, Nilufer G. Concordant loss offragile gene expression early in breast calleer development[J]. Pathology International,2005, 55(8):471-475.
  • 2邵霞,王修珍.抑癌基因FHIT在乳腺癌中的表达及其临床意义[J].苏州大学学报(医学版),2008,28(4):614-616. 被引量:2
  • 3Huiping C, Kristjansdottir S,Bergthorsson J T,et al. High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancer[J]. EurJ Cancer,2002, 38(5) :728-735.
  • 4Toledo G,Sola J J,Lozano M D,et al. Loss of FHIT protein expression is related to high proliferation, low apoptosis and worse prognosis in non-small cell lung cancer[J]. Mod Pathol, 2004, 17(4) : 440-448.
  • 5Butler D,Collins C,Mabrok M,et al. Loss of Fhit expression as a potential marker of malignant progression in preinvasive squamous cervical cancer[J]. Gyneeol Oncol, 2002, 86 (2) : 144-149.
  • 6Pichiorri F,Trapasso F,Palumbo T,et al. Preclinical assessment of FHIT gene replacement therapy in human leukemia using a ehimerie adenovirus, Ad5/F35[J]. Clin Cancer Res, 2006, 12 (11 Pt 1): 3494-3501.
  • 7Roz L,Gramegna M, Ishii H, et al. Restoration of fragile histidine triad (FHIT) expression induces apoptosls and suppresses tumorigenicity in lung and cervical cancer cell lines[J]. Proe Natl Acad Sci U S A, 2002,99(6): 3615-3620.
  • 8Ishii H, Umon K, Vecchione A, et al. Effect of adnoviral transduction of the fragile histidine triad gene into esophageal cancer cells[J]. Cancer Res, 2001,6(4) : 1578-1584.
  • 9王俊,段晓明,周自华,贺修胜.外源性FHIT基因表达对长春新碱诱导人胃癌MKN-28细胞凋亡的影响[J].世界华人消化杂志,2008,16(30):3367-3371. 被引量:2
  • 10张立群,汪蕙,赖百塘,王玥.外源FHIT基因对不同FHIT基因状态肺癌细胞系恶性增殖的影响及其机理的研究[J].解剖学报,2005,36(5):513-518. 被引量:1

二级参考文献24

  • 1张立群,汪蕙,赖百塘,岳文涛,杨学惠,张春燕.FHIT转染人肺癌单克隆细胞的建立及对生长的抑制[J].结核病与胸部肿瘤,2004(2):98-103. 被引量:3
  • 2李铭,袁宏银.FHIT基因与肿瘤[J].数理医药学杂志,2006,19(2):187-190. 被引量:3
  • 3Da-Long Wu,Ying Xu,Li-Xin Yin,Huan-Zhang Lu.Reversal of multidrug resistance in vincristine-resistant human gastric cancer cell line SGC7901/VCR by LY980503[J].World Journal of Gastroenterology,2007,13(15):2234-2237. 被引量:3
  • 4Siprashvili Z, Sozzi G, Barnes LD, et al. Replacement of FHIT in cancer cells suppresses tumorigenicit [ J]. Proc Natl Acad Sci USA,1997,94(25) :13771-13776.
  • 5Roz L, Gramegna M, Ishii H, et al. Restoration of frigle histidine triad (FHIT) expression induces apoptosis and suppresses tumorigenicity in lung and cervical cancer cell lines [ J]. Proc Natl Acad Sci USA,2002,99(6) :3615-3620.
  • 6Ishii H, Zanesi N, Vecchione A, et al. Regression of upper gastric cancer in mice by FHIT gene delivery [ J ]. FASEB J, 2003, 17 (12):1768-1770.
  • 7Sozzi Geronese ML, Negrini M, et al. FHIT gene at 3p14.2 is abnomal in lung cancer [ J]. Cell, 1996,85 ( 1 ): 17-26.
  • 8Wu R,Connolly DC, Dunn RL, et al. Restored expression of fragile histidine trial protein and tumorigenicity of cervical carcinoma cells [J].J Natl Cancer Inst, 2000,92(4):338-344.
  • 9Otten GA, Xiao GH, Geradts J, et al. Protein expression and functional analysis of the FHIT gene in human tumor cells[J]. J Natl Cancer Inst, 1998,90(6) :426-432.
  • 10Ishii H, Dumon KR, Vecchione A, et al. Effect of adenoviral transduction of the fragile histidine triad gene into esophageal cancer cells[J]. Cancer Res, 2001,61(4): 1578-1584.

共引文献2

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