Although 1, 2 and pifithrin-α caused serious inhibition on p53, 1 and 2 significantly cause the loss of mitochondrial membrane potential and increase of the reactive oxygen species level, cytochrome c, apaf-1 and caspase-3/9 ratio in BEL-7404 cells. 1 and 2 may trigger the cell apoptosis through a mitochondrial dysfunction pathway whereas pifithrin-α does not. The interactions of 1 and 2 with DNA are most
[Pt(Q)2 ](1)和[Pt(MQ)2 ](2)对BEL-7404,Hep-G2,NCI-H460,T-24,A549肿瘤细胞表现出增强的细胞毒性,但对正常HL的细胞毒性较低-7702细胞。1和2可能分别导致细胞周期停滞在G2和S期。特定的p53
抑制剂pifithrin-α诱导细胞周期停滞在G1期。尽管1,2和pifithrin-α引起的对p53,严重抑制1和2显著原因线粒体膜电位和活性氧物质的
水平,细胞色素增加的损失Ç,BEL-7404细胞中apaf-1和caspase-3 / 9的比例。1和2可能通过线粒体功能障碍途径触发细胞凋亡,而pifithrin-α则不会。1和2与DNA的相互作用极有可能是通过插层作用。