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干扰素对MCF-7乳腺癌细胞的增殖抑制作用 被引量:1

DEPRESSANT EFFECTS OF INTERFERON ON PROLIFERATION OF MCF-7 BREAST CANCER CELLS
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摘要 目的:研究干扰素对MCF-7乳腺癌细胞的增殖抑制作用。方法:MTT法检测干扰素-γ(IFN-γ)、干扰素-α2b(IFN-α2b)单独及联合应用,作用不同时间对MCF-7乳腺癌细胞的增殖抑制作用。结果:IFN-γ、IFN-α2b及二者联合应用均对MCF-7乳腺癌细胞的增殖具有抑制作用:单独用药时,作用48h的抑制作用较为明显(P<0.05);联合用药时,作用72h效果显著(P<0.05)。结论:IFN-γ、IFN-α2b及二者联合应用对MCF-7乳腺癌细胞增殖均有不同程度的抑制作用,二者联合应用药效作用时间延长、作用效果更佳。 Objective:To investigate the depressant effects of interferon on proliferation of MCF-7 breast cancer cells.Methods:MTT method was used to detect the depressant effects of interferon-γ(IFN-γ),interferon-α2b(IFN-α2b) alone or combination on proliferation of MCF-7 breast cancer cells with different action times.Results:IFN-γ,IFN-α2b alone or combination all had depressant effects on proliferation of MCF-7 breast cancer cells:the depressant effects at 48h was fairly obvious when administrated the interferon alone(P〈0.05);the depressant effects at 72h was significant when combined the interferon(P〈0.05).Conclusions:IFN-γ,IFN-α2b alone or combination all have different depressant effects on proliferation of MCF-7 breast cancer cells.The action time is more longer and the effects is more better of combination.
出处 《承德医学院学报》 2010年第2期131-133,共3页 Journal of Chengde Medical University
关键词 IFN-Α2B IFN-Γ MCF-7乳腺癌细胞 MTT法 IFN-α2b IFN-γ MCF-7 breast cells MTT method
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  • 1M.Amling,M.Psl,I.Bsler,G.Delling,阮幼冰.凋落:Bcl-2是程序性细胞死亡的关键蛋白[J].德国医学,1996,13(1):58-60. 被引量:6
  • 2Blankenstein T,Oin Z.The role of IFN—gamma in tumor transplantation immunity and inhibition of chemical carcinogenesis.Curr Opin Immunol,2003.15:148—154.
  • 3Van Deusen J B,Caligiuri Ma.New developments in anti-tumor efficacy and malignant transformation of human natural killer cells、Curr Opin Hematol.2003.10:55—59.
  • 4Chawla—Sarkar M,Lindner D J,Liu Y F.et a1.Apoptosis and interferons:role of interferon—stimulated genes as mediators of apoptosis.Apoptosis,2003,8:237—249.
  • 5Malusecka E,Zbouek A, Krzyzowska-Gruca S, et al. Changes in expression of PRB, P16 and cyclinD1 in non-small cell lung cancer an immunohistochemical study. Folia Histochem Cytobiol, 1999,37(1):19-24.
  • 6Lindeman B, Skarpen E, Thoresen TH, et al. Alteration of G1 cell -cycle protein expression and induction of P53 but not P21/wafl by the DNA- modifying carcinogen 2- acetylamin of uorence in growthstimulated hepatocytes in vitro. Mol Carcinog, 1999,24 ( 1 ):36-46.
  • 7Miyoshita T, Harigai M, Hanada M, et al. Identification of a P53-dependent negative response element in the Bcl- 2 gene. Cancer Res, 1994,54:3131 -3135.
  • 8Johnstone R W, Wei W, Greenway A, et al. Functional interaction between p53 and the interferon-inducible nucleoprotein IFI 16[J]. Oncogene, 2000,19(52):6033-6042.
  • 9Dornan D, Eckert M, Wallace M, et al. Interferon regulatory factor 1 binding to p300 stimulates DNA-dependent acetylation of p53[J]. Mol Cell Biol,2004,24(22):10083-10098.
  • 10Wiley S R, Schooley K, Smolak P J, et al .Identification and characterization of a new member of the TNF family that induce apoptosis[J].Immunity,1995,3(6):673-682.

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