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茶多酚在骨肉瘤顺铂化疗中增效作用的实验研究 被引量:7

Enhancement effect of tea polyphenols combined with cisplatin on osteosarcoma S-SLM cell line
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摘要 目的探讨茶多酚在骨肉瘤细胞株顺铂化疗中的增效作用。方法骨肉瘤细胞株分别经茶多酚、顺铂、茶多酚+顺铂作用72h,采用体外细胞毒性试验观察三者的细胞毒性;应用流式细胞仪分析茶多酚、顺铂及二者配伍对骨肉瘤细胞株的细胞周期的影响。结果骨肉瘤细胞株与浓度为50、100、200、400μg/ml的茶多酚作用时,其细胞毒性指数分别为9.62%、12.30%、28.85%、46.15%,与空白对照组比较差异有统计学意义(F=128.82,P<0.05)。与浓度为0.1、1.0、10.0、100.0μg/ml的顺铂作用时,其细胞毒性指数分别为24.04%、54.80%、65.38%、88.46%,与空格对照组比较,差异有统计学意义(F=75.97,P<0.05)。而低浓度茶多酚与顺铂联合作用,其细胞毒性指数明显增加,随着各自浓度的升高,其细胞毒性作用明显增加。应用流式细胞仪分析显示,茶多酚对细胞周期也有明显的影响,使G0与G1期细胞比例明显增加(F=32.50,P<0.05),G2与M期细胞比例明显减少(F=8.32,P<0.05),S期比例无明显改变。结论茶多酚在骨肉瘤细胞株顺铂化疗中有显著的增效作用,并能改变骨肉瘤细胞的细胞周期。 Objective To observe the cytotoxicity effect of tea polyphenols combined with cisplatin on osteosarcoma S-SLM cell line.Methods The osteosarcoma S-SLM cell line was treated with different concentration tea polyphenols,cisplatin,tea polyphenols+cisplatin for 72 hours,respectively,by using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide(MTT) assay in vitro,the cytotoxicity effect were observed;By using flow cytometry(FCM),the cell cycle phases were analyzed.Results Osteosarcoma cell line(S-SLM) was treated with different concentration of tea polyphenols(50,100,200,400 μg/ml),the cytotoxicity index were 9.62%,12.30%,28.85%,46.15%,compared with the control group,the difference was significant(F=128.82,P0.05).And treated with different concentration of cisplatin(0.1,1.0,10.0,100.0 μg/ml),the cytotoxicity index were 24.04%,54.80%,65.38% and 88.46% compared with the space group,the difference was significant(F=75.97,P0.05).The cytotoxicity index increased obviously as the concentration of tea polyphenols or cisplatin increased.While treated with tea polyphenols and cisplatin simultaneously,the cytotoxicity index increased obviously.The cell cycle of the treated S-SLM cell line was changed with marked increasing in G0/G1 phase fraction and decreasing in G2/M phase fraction(F=32.50,8.32,P0.05),and S phase fraction did not change significantly.Conclusions Tea polyphenols combined with cisplatin had enhancement cytotoxicity effect on osteosarcoma S-SLM cell line,and also can change the cell cycle of the treated S-SLM cell line.
出处 《全科医学临床与教育》 2011年第1期34-37,共4页 Clinical Education of General Practice
基金 浙江省中医药科技计划基金(2005C047)
关键词 骨肉瘤 茶多酚 顺铂 肿瘤细胞 osteosarcoma tea polyphenols cisplatin tumor cells
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参考文献9

  • 1Gottesman MM,Pastan L,Ambudkar SV.P-glyeopmtein and muhidrug resistance [J].Curr Opin Genet Dev, 1996,6 (5) : 6- 10.
  • 2Donna M, Bardshaw, Robert J, et al.Clinical relevance of transmembrane drug as a mechanism of muhidrug resistance[J]. Journal of Clinical Oncology, 1998,16(11) : 3674-3690.
  • 3Tsuchiya H, Tomita K, Mori Y, et al. Caffeine assisted chemotherapy and minimized tumor excision for nonmet- astatic osteosarcoma[J]. Cancer Res,1998,18(1B):657-666.
  • 4Tsuchiya H, Tomita K, Mori Y, et al. Marginal excision for osteosarcoma with Caffeine assisted chemotherapy[J]. Clin Orthop, 1999,30(358):27-35.
  • 5刘刚,陆劲松,邵志敏,沈镇宙.茶多酚对肿瘤防治作用的研究进展[J].中国癌症杂志,2002,12(3):265-268. 被引量:15
  • 6Yang CS,Wang ZY.Tea and cancer [J]. J Natl cancer Inst , 1993,85(13):1038-1039.
  • 7Yasutake H, Tsuchiya H, Tomita K, et al. Inhibitory effect of Caffeine on potentially lethal damage repair in cisplatin treated human osteosarcoma cells. Anticancer Res,1995,15 (3):831-837.
  • 8Puck TY, Johnson R, Webb P. Mutation inhibition by beta- estradial after low doses of gamma-irradiation of mammmalion cells[J]. Somat Cell Mol Geet,1999,25(2):59-65.
  • 9刘春选,戴刚,张祥生,王秉义.人骨肉瘤细胞MTT法药敏试验及应用[J].中华骨科杂志,1997,17(12):754-756. 被引量:7

二级参考文献26

  • 1张春燕,赵清正,王萍,郭素萍,赵玖,白瑾峰,程书钧.促癌剂对基因表达的影响[J].中国医学科学院学报,1995,17(1):11-15. 被引量:4
  • 2[1]Yang CS, Wang ZY. Tea and cancer[J]. J Natl Cancer Inst,1993, 85(13): 1038-1039.
  • 3[2]Graham HN. Green tea composition, consumption, and polyphenolchemistry[J]. Prev Med,1992,21(3): 334-350.
  • 4[3]Wang ZY, Huang MT, Lon YR, et al. Inhibition effects of black tea, green tea, decaffeinated black tea and decaffeinated green tea on ultroviolet B light-induced skin carcinogenesis in 7,12-Dimethylbenz(α)anthracene-initiated SKH-mice[J]. Cancer Res,1994,54(13):3428-3435.
  • 5[4]Huang MT, Xie JG, Wang ZY, et al. Effects of tea, decaffeinated tea and caffein on UVB light-induced complete carcinogenesis in SKH-1 mice: Demonstration of caffenin as a biologically important constituent of tea[J]. Cancer Res,1997,57(13): 2623-2629.
  • 6[5]Gensler HL, Timmermann BN, Valcic S, et al. Prevention of photocarcinogenesis by topical administration of pure epigallocatechin gallate isolated from green tea[J]. Nutr Cancer,1996,26(3): 325-335.
  • 7[6]Wang ZY, Wang LD, Lee MJ, et al. Inhibition of N-nitrosomethylbenzylamine-induced esophageal tumorigenesis in rats by green and black tea[J].Carcinogenesis,1995,16(9): 2143-2148.
  • 8[7]Wang ZY, Hong JY, Huang MT, et al. Inhibition of N-nitrosodiethylanime and 4-(methylnitrosamino)-1-(3-pridyl)-rbutanone-induced tumorigenesis in A/J mice by green tea and black tea[J]. Cancer Res,1992,52(7): 1943-1947.
  • 9[8]Yan YS. The experiment of tumor-inhibiting effect of green tea extract in animals and humans[J]. Chung-Hua Yu Fang I Hsueh Tsa Chih,1993,27(3):129-131.
  • 10[9]Yang CS, Lee MJ, Chen L, et al. Polyphenols as inhibitors of carcinogenesis[J].Envirol Health Perspect,1997,105(S4):971-976.

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