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CCK-8法检测表没食子儿茶素没食子酸酯对胰腺癌PANC-1细胞增殖的抑制作用 被引量:1

Inhibitory effects of epigallocatechin-3-gallate (EGCG) on cell proliferation in human pancreatic carcinoma PANC-1 cells
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摘要 目的检测表没食子儿茶素没食子酸酯(epigallocatechin-3-gallate,EGCG)对体外培养的人胰腺癌细胞系PANC-1增殖的影响。方法缺氧条件下体外培养胰腺癌PANC-1细胞,外源性给予不同剂量的EGCG(10、20、40、60、80、100、160μg/mL)作用细胞不同时间(12、24、48 h),CCK-8法检测不同浓度药物对胰腺癌细胞增殖的影响。结果 EGCG可显著抑制人胰腺癌细胞PANC-1的增殖,其抑制率在药物浓度和时间上呈剂量依赖性和时间依赖性关系;160μg/mL EGCG作用48 h后,PANC-1细胞的生长抑制率高达(91.03±2.32)%。结论 EGCG对体外缺氧培养的人胰腺癌细胞系PANC-1的增殖有显著抑制作用。 Objective To investigate the inhibitory effects of epigallocatechin-3-gallate(EGCG) on cell proliferation in human pancreatic carcinoma PANC-1 cell lines.Methods The human pancreatic carcinoma PANC-1 cell lines were incubated under hypoxic condition.Different concentrations of EGCG(10,20,40,60,80,100,160 μg/mL) were applied in cells in vitro for different times(12,24,48 hours).CCK-8 method was used to investigate the effects of drugs on cell proliferation.Results EGCG could inhibit significantly the proliferation of human pancreatic carcinoma PANC-1 cell lines in concentration-dependent and time-dependent manner.There were strong(obvious) inhibition(91.03 ±2.32) % of EGCG(160 μg/mL) on cell proliferation after 48 h treatment.Conclusion EGCG could inhibit significantly the proliferation of human pancreatic carcinoma PANC-1 cell lines in the hypoxic microenvironment.
出处 《胃肠病学和肝病学杂志》 CAS 2010年第10期936-938,共3页 Chinese Journal of Gastroenterology and Hepatology
关键词 表没食子儿茶素没食子酸酯 CCK-8 胰腺癌 缺氧 Epigallocatechin-3-gallate CCK-8 Pancreatic carcinoma Hypoxic
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  • 1Semenza GL. Targeting HIF-1 for cancer therapy [ J]. Nat Rev Cancer, 2003, 3(10) : 721-732.
  • 2Lin SK, Shun CT, Kok SH, et al. Hypoxia-stimulated vascular endothelial growth factor production in human nasal polyp fibroblasts: effect of epigallocatechin-3-gallate on hypoxia-inducible factor-1 alpha synthesis [ J]. Arch Otolaryngol Head Neck Surg, 2008, 134 (5) : 522-527.
  • 3Lieber M, Mazzetta J, Nelson-Rees W, et al. Establishment of a continuous tumor-cell line ( panc-1 ) from a human carcinoma of the exocrine pancreas [J]. Int J Cancer, 1975, 15(5): 741-747.
  • 4Hehnlinger G, Yuan F, Dellian M, et al. Interstitial PH and p02 gradients in solid tumor in vivo: high-resolution measurements reveal a lack of correlation [J]. Nat Med, 1997, 3(2): 177-182.
  • 5Bergman AM, Pinedo HM, Peters GJ. Determinants of resistance to 2', 2'-difluorodeoxycytidine ( gemcitabine ) [J]. Drug Resist Updat, 2002, 5(1): 19-33.
  • 6Comerford KM, wallaceTJ, Karhausen JNI, et al. Hypoxia-inducible factor-1-dependent regulation of the multidrug resistance (MDR1) gene [J]. Caneer Res, 2002, 62(12): 3387-3394.
  • 7Fujiki H, Suganuma M, Imai K, et al. Green tea: cancer preventive beverage and/or drug [ J ]. Cancer Lett, 2002, 188 ( 1-2 ) : 9-13.
  • 8Lin JK, Liang YC. Cancer prevention by teapolyphenols [ J]. Proc Natl Sci, 2000, 24(1): 1-13.
  • 9Wang YC, Bachraeh U. The specific anti-cancer activity of green tea EGCG [J]. Amino Acids, 2002, 22(2): 131-143.
  • 10Kushima Y, Iida K, Nagaoka Y, et al. Inhibitory effect of (-)-epigal- locatechin and (-)-epigallocatechin gallate against heregulin betal-in-duced migration/invasion of the MCF-7 breast carcinoma cell line[ J]. Biol Pharm Bull, 2009, 32 (5) : 899-904.

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