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青蒿琥酯对黑素瘤A875细胞增殖和凋亡的影响及机制研究 被引量:1

Effect of artesunate on the proliferation and apoptosis of melanoma A875 cells
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摘要 目的观察青蒿琥酯对人皮肤恶性黑素瘤A875细胞增殖和凋亡的影响,并探讨相关机制。方法体外培养A875细胞,分别给予不同浓度的青蒿琥酯(10~80μg/rnl)作用细胞48h,MTT法检测抑制率,流式细胞术检测凋亡率,Westernblot法检测Caspase-3、Caspase-8、Caspase-9的蛋白表述水平变化。结果青蒿琥酯对A875细胞有明显的生长抑制和诱导凋亡的作用(P〈0.01),呈剂量依赖性;随药物浓度的增高.Caspase-3、Caspase-8、Caspase-9的蛋白表达量逐渐升高(P〈0.05)。结论青蒿琥酯可以通过死亡受体途径和线粒体途径诱导A875细胞的凋亡,从而抑制细胞增殖。 Objective To investigate the influence of artesunate on the proliferation and apoptosis of human skin malignant melanoma A875 cells, and to explore its possible action mechanism. Methods The A875 cells were cultured with different concentration (10p, g/ml -80lμ/ml) of artesunate for 48 hours in vitro. The inhibition ratio was examined by MTr method, and apoptotic rate was detected by flow cytometry. The changes of protein expression of Caspase-3, Caspase-8 and Caspase-9 were detected by Western Blot. Results A875 cells proliferation was significantly inhibited by artesunate in a concentration-dependent manner. The apoptosis of A875 cells was accelerated in a concentration-dependent manner too. With the increase of drug concentration, the protein expression levels of Caspase-3, Caspase-8 and Caspase-9 were gradually increased. Conclusion Artesunate can induce apoptosis of A875 cells via death receptor pathway and mitochondrial pathway, as a result, artesunate has an obvious inhibition effect on A875 cells proliferation.
出处 《河北医药》 CAS 2013年第16期2408-2410,共3页 Hebei Medical Journal
关键词 黑素瘤 青蒿琥酯 细胞凋亡 melanoma artesunate apoptosis
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  • 1Hodi FS, O "Day SJ, Mcdermott DF, et al. Improved survival with ipili- mumab in patients with metastatic melanoma. New England Journal of Medicine ,2010,363:711-723.
  • 2Bhatia S, Tykodi SS, Thompson JA. Treatment of metastatic melanoma: an overview. Oneology ,2009,23:488-496.
  • 3Boeckmann L, Schirmer M, Rosenberger A, et al. Effect of DNA repair host factors on temozolomide or dacarbazine melanoma treatment in Cau- casians. Pharmacogenetics and genomics ,2009,19:760-769.
  • 4Rasheed SAK,Efferth T,Asangani IA,et al. First evidence that the anti- malarial drug artesunate inhibits invasion and in vivo metastasis in lung cancer by targeting essential extracellular proteases. International Journal of Cancer,2010,127 : 1475-1485.
  • 5Wang Y, Han Y, Yang Y, et al. Effect of interaction of magnetic nanopar- tieles of Fe304 and artesunate on apoptosis of K562 cells. International journal of nanomedicine ,2011,10 : 1185-1192.
  • 6Xu L, Yuan S, Li J, et al. The conservation and uniqueness of the caspase family in the basal chordate,amphioxus. BMC biology ,2011,9:60-73.
  • 7Sayers TJ. Targeting the extrinsic apoptosis signaling pathway for cancer therapy. Cancer Immunology. Immunotherapy ,2011,60 : 1173-1180.
  • 8Reubold TF, Wohlgemuth S, Eschenburg S. Crystal structure of full-length apaf-1 :how the death signal is relayed in the mitochondrial pathway of apoptosis. Structure,2011,19 : 1074-1083.
  • 9Mazumder S, Plesea D, Almasan A. Caspase-3 activation is a critical de- terminant of genotoxic stress-induced apoptosis. Methods Mol Biol,2008, 414..13-21.

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