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Chinese Journal of Oncology Prevention and Treatment ›› 2011, Vol. 3 ›› Issue (2): 103-.doi: 10.3969/j.issn.1674-5671.2011.02.02

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HUANG Wen-Feng, XIE Wei-Min, WANG Hong-Xue, LU Yong-Kui, ZHOU Wen-Xian   

  • Online:2011-08-03 Published:2011-08-03
  • Supported by:

    国家自然科学基金资助项目(30960436);广西卫生厅科研课题(Z2009240、Z2009251)

Abstract: 【Abstract】ObjectiveTo study the damage effect of lobaplatin (LBP) and cisplatin (DDP) on human umbilical vein endothelia cell line (HUVECs),human liver cell line (QSG7701) and human renal tubular epithelial cells (HK-2 cells),and to explore the possible mechanismMethodsThe proliferation responses of HUVECs,QSG-7701 and HK2 cells treated with LBP or DDP in the concentration of 3.125ug/ml were observed by MTT assayIn addition,the concentrations of malondialdehyde (MDA) and superoxide dismutase (SOD) were determined in HK2 cellsResultsWith the same concentration and action time,the inhibition effect of DDP on HK2 cells was significantly higher than that of LBP (P<0.05),while the inhibition effect of LBP on HUVECs was significantly higher that that of DDP (P<0.05)The inhibition rate of these two drugs on QSG7701 was not significantly different (P>0.05)The level of MDA in LBPtreated group or DDPtreated group was significantly higher than that in control group (P<0.05),the level of SOD in both platinum groups was significantly lower than that in control group (P<0.05),while both the levels of MAD and SOD were not significantly different between LBPtreated group and DDPtreated group (both P>0.05)Conclusion LBP and DDP displayed inhibitive effect on human hepatocytes and renal tubular epithelial cellsLBP might have stronger antiangiogenesis effect on HUVECs comparing to DDPOxidative damage may be a common mechanism of renal toxicity caused by LBP and DDP

Key words: 【Key words】 Platinum, HUVECs, QSG-7701, HK-2 , cells