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雷帕霉素单独及联合化疗药物应用对胃癌细胞生长的影响 被引量:3

Effect of rapamycin combination chemotherapy drugs on inhibition of gastric cancer cells
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摘要 目的:研究mTOR抑制剂雷帕霉素对SGC-7901胃癌细胞增殖的影响及其可能的机制,并探讨其与传统化疗药物的联合作用。方法:体外培养胃癌SGC-7901细胞,取对数生长期的细胞进行试验,用不同浓度的mTOR抑制剂雷帕霉素以及长春新碱分别作用于胃癌SGC-7901细胞24、48、72小时,用MTT法检测雷帕霉素单独以及联合化疗药物对其生长的影响。用流式细胞术检测mTOR抑制剂雷帕霉素、长春新碱单独以及联合应用对胃癌SGC-7901细胞周期的影响。结果:MTT法结果显示:雷帕霉素单独能够显著抑制胃癌SGC-7901细胞的增殖,其作用随着药物浓度以及作用时间的增加而增加,呈现时间-剂量效应关系;与化疗药物长春新碱联合应用其抑制效应明显增强。流式细胞术检测结果显示:雷帕霉素、长春新碱单独作用胃癌细胞将细胞周期主要阻滞在G_0/G_1期,而联合给药时G_0/G_1期比例增加。结论:mTOR抑制剂雷帕霉素能够显著抑制胃癌SGC-7901细胞的增殖,其机制可能与通过阻滞细胞周期在G_0/G_1期相关;并且雷帕霉素可提高传统化疗药物长春新碱对胃癌细胞的敏感性。_ Objective:To investigate the influence of rapamycin on human gastric cancer SGC -7901 cells prolif-eration and its mechanism.Methods:Gastric cancer cells SGC -7901 were cultured and treated with rapamycin,vin-cristine and combination of the two.Then the inhibitory effects of the three medications on the growth of the SGC -7901 cells were determined by MTT,and their cell cycle were detected by flow cytometry.Results:Compared with the control group,the three medications all significantly inhibited the proliferation of SGC -7901 cells,and the combined method enhanced the effect.Flow cytometry showed that rapamycin and vincristine blocked the cell cycle mainly in the G0 /G1 stage,the combined medication enhanced this effect.Conclusion:Rapamycin can inhibit the proliferation of SGC -7901 cells and enhance the chemosensitivity of gastric cancer.
出处 《现代肿瘤医学》 CAS 2016年第13期2019-2022,共4页 Journal of Modern Oncology
关键词 雷帕霉素 哺乳动物雷帕霉素靶蛋白 胃癌 化疗敏感性 rapamycin, mammals rapamycin target protein, gastric cancer, ehemosensitivity
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  • 1Fang Y,Vilella-Bach M,Bachmann R,et al.Phosphatidic acid mediated mitogenie aactivation of mTOR signaling[J].Science,2001,294(5548):1942-1945.
  • 2贾海泉,蔺会云,徐元基,等.MAG-1对肿瘤细胞迁移、黏附和侵袭能力的影响及其作用机制的研究[C].第五届中国肿瘤学术大会暨第七届海峡两岸肿瘤学术会议、国际肿瘤细胞与基因治疗学术会议、第二届中日肿瘤介入治疗学术会议论文集,2008:190-205.
  • 3Wang Y,Jia H,Lin H,et al.Metastasis-associated gene,MAG-1 improves tumor microenvironmental adaptation and potentiates tumor metastasis[J].J Cell Mol Med,2012,16(12):3037-3051.
  • 4Joseph Avruch,Xiaomeng Long,Yenshou Lin,et al.Activation of mTORC1 in two steps:Rheb-GTP activation of catalytic function and increased binding of substrates to raptor[J].Biochem Society Transactions,2009,37(1):223-226.
  • 5Ryan C Russell,Chong Fang,Kun-Liang Guan.An emerging role for TOR signaling in mammalian tissue and stem cell physiology[J].Development,2011,138(16):3343-3356.
  • 6Weichhart T,Costantino G,Poglitsch M,et al.The TSC-mTOR signaling pathway regulates the innate inflammatory response[J].Immun,2008,29(4):565-577.
  • 7Zhang YJ,Bao YJ,Dai Q,et al.mTOR signaling is involved in indomethacin and nimesulide suppression of colorectal cancer cell growth via a COX-2 independent pathway[J].Ann Surg Oncol,2011,18(2):580-588.
  • 8Powell JD,Delgoffe GM.The mammalian target of rapamycin:linking T cell differentiation,function,and metabolism[J].Immunity,2010,33(3):301-311.
  • 9Layne AS,Nasrallah S,South MA,et al.Impaired muscle AMPK activation in the metabolic syndrome may attenuate improved insulin action after exercise training[J].J Clin Endocrinol Metab,2011,96(6):1815-1826.
  • 10Lei Liu,Yang Luo,Long Chen,et al.Rapamycin inhibits cytoskeleton reorganization and cell motility by suppressing RhoA expression and activity[J].J Biol Chem,2010,285(49):38362-38373.

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