State Key Laboratory Cultivation Base for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry & Pharmacy of Guangxi Normal University, Guilin 541004, PR China.
State Key Laboratory Cultivation Base for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry & Pharmacy of Guangxi Normal University, Guilin 541004, PR China.
Eur J Med Chem. 2015 Mar 6;92:302-13. doi: 10.1016/j.ejmech.2014.12.052. Epub 2014 Dec 30.
[Pt(Q)2] (1) and [Pt(MQ)2] (2) exhibited enhanced cytotoxicity against BEL-7404, Hep-G2, NCI-H460, T-24, A549 tumor cells but low cytotoxicity on normal HL-7702 cells. 1 and 2 could cause the cell cycle arrest in G2 and S phase, respectively. While pifithrin-α, a specific p53 inhibitor, induced cell cycle arrest in G1 phase. 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 probably via an intercalation.
[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-7702 细胞的细胞毒性较低。1 和 2 分别可导致细胞周期停滞在 G2 和 S 期。虽然 pifithrin-α,一种特定的 p53 抑制剂,可诱导细胞周期停滞在 G1 期。尽管 1、2 和 pifithrin-α对 p53 有严重的抑制作用,但 1 和 2 可显著导致 BEL-7404 细胞中线粒体膜电位的丧失和活性氧水平、细胞色素 c、凋亡酶激活因子-1 和半胱天冬酶-3/9 比值的增加。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 的相互作用很可能是通过嵌入发生的。