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丹参酮ⅡA对MKN-45细胞生长的影响 被引量:13

Effect of Tanshinone ⅡA on the growth of MKN-45 cell line in vitro
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摘要 目的:研究丹参酮ⅡA(Tanshi-noneⅡA,TanⅡA)对人胃癌细胞株MKN-45的生长抑制作用。方法:选用人胃癌细胞株MKN-45,运用MTT法、流式细胞术(FCM)和逆转录聚合酶链式反应(RT-PCR)半定量法检测细胞增殖、细胞周期、细胞凋亡和各组p53mRNA表达。结果:TanⅡA可明显抑制MKN-45细胞的增殖,其抑制作用具有时间-效应和剂量-效应关系。当2·0μg/mL TanⅡA处理MKN-45细胞96h,增殖抑制率达(74·84±0·41)%。FCM检测肿瘤细胞DNA变化,观察到TanⅡA使MKN-45细胞周期阻滞于G2/M期,出现浓度依赖性的亚“G1”峰,同时野生型p53表达增加。结论:TanⅡA能有效地抑制人胃癌细胞株MKN-45的增殖,其可能的机制与凋亡有关。肿瘤防治杂志,2005,12(19) OBJECTIVE: To investigate the effect of Tanshinone Ⅱ A on the growth of human gastric carcinoma cell line MKN- 45 in vitro. METHODS: Cell proliferation,cell cycle and apoptosis, the expression of p53 mRNA of cell line MKN-45 were detected by MTT assay, flow cytometry (FCM) and semiquantitative RT-PCR. RESULTS: The data showed that Tanshinone Ⅱ A effectively inhibited the proliferation of cell line MKN-45 in time- and concentrationdependent. The cell proliferation inhibition rate was (74.84 ± 0.41)% when treated with 2.0 μg/mL Tanshinone Ⅱ A for 96 hours. The change of DNA of MKN-45 cells indicated that Tanshinone Ⅱ A was able to block cell cycle progress in G2/M phase,with appearance of sub-G1 peak in a concentration- dependently. The expression of p53 was up-regulated in the process of Tanshinone Ⅱ A - inducing MKN-45 apoptosis. CONCLUSION: Tanshinone Ⅱ A can effectively inhibit the proliferation of human gastric carcinoma cell line MKN-45 in vitro and the possible mechanism may relate to modulation of the apoptosis associated gene expression, such as p53 up-regulated.
出处 《肿瘤防治杂志》 CAS 2005年第19期1465-1468,共4页 China Journal of Cancer Prevention and Treatment
关键词 胃肿瘤/病理学 丹参酮/药理学 细胞凋亡/药物作用 蛋白质P53 stomach neoplasms/pathology tanshinone/pharmacology apoptosis/drug therapy protein p53
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  • 1黄光琦,袁淑兰,周宏远,王修杰,江映红.丹参酮诱导人宫颈癌ME180细胞的分化[J].中国药理学与毒理学杂志,1996,10(4):285-289. 被引量:16
  • 2Vrionis FD, Wu JK, Qi P, et al. The bystander effect exerted by tumor cells expressing the herpes simplex virus thymidine kinase (HSVtk) gene is dependent on connexin expression and cell communication via gap junctions. Gene Ther, 1997,4: 577-585.
  • 3Carystinos GD, Alaoni-Jamali MA, Phipps J,et al. Upregulation of gap junctional intercellular communication and connexin 43 expression by cyclic-AMP and all-trans-retinoic acid is associated with glutathione depletion and chemosensitivity in neuroblastorm cells. Cancer Chemother Pharmacol,2001, 47:126-132.
  • 4Oviedo-Orta E, Hoy T, Eanvs WH. Intercellular communication in the immune system: differential expression of connexin40 and 43, and perturbation of gap junction channel functions in peripheral blood and tonsil human lymphocyte subpopulations. Immunology, 2000, 99: 578-590.
  • 5Goodenough DA, Goliger JA, Paul DL. Connexins, connexons, and intercellular communication. Annu Rev Biochem , 1996,65:475-502.
  • 6Marconi P, Tamura M, Moriuchi S, et al. Connexin 43-enhanced suicide gene therapy using herpesviral vectors. Mol Ther, 2000, 1 : 71-81.
  • 7Sanson M, Marcaud V, Robin E, et al. Connexin 43-mediated bystander effect in two rat glioma cell models. Cancer Gene Ther, 2002,9: 149-155.
  • 8Laird DW, Fistouris P, Batist G, et al. Deficiency of connexin43 gap junctions is an independent marker for breast tumors. Cancer Res, 1999,59:4104-4110.
  • 9Trosko JE, Chang CC. Mechanism of up-regulated gap junctional intercellular communication during chemoprevention and chemotherapy of cancer. Mutat Res, 2001, 480-481:219-229.
  • 10Ito Y. Review: Recent advances in counter-current chromatography. Journal of Chromatography, 1991, 538: 3-25

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