Department of Dermatology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama, Japan.
Free Radic Res. 2011 Mar;45(3):326-35. doi: 10.3109/10715762.2010.532494. Epub 2010 Nov 3.
Platinum nanoparticles (Pt-NPs) are known to possess anti-tumouric activity and the ability to scavenge superoxides and peroxides indicating that they can act as superoxide dismutase (SOD)/catalase mimetics. These potentials seem useful in the protection and/or amelioration of oxidative stress-associated pathologies, but, when they are combined with a therapeutic modality that depends upon the mediation of reactive oxygen species in cell killing induction, the effect of Pt-NPs might be questionable. Here, the effects of polyacrylic acid-capped Pt-NPs (nano-Pts) on hyperthermia (HT)-induced apoptosis and the underlying molecular mechanisms were investigated in human myelomonocytic lymphoma U937 and human cutaneous T-cell lymphoma HH cells. The results showed that the pre-treatment with nano-Pts significantly inhibited HT-induced apoptosis in a dose-dependent manner. Superoxide, but not peroxides, was suppressed to varying extents. All pathways involved in apoptosis execution were also negatively affected. The results reveal that the combination of nano-Pts and HT could result in HT-desensitization.
铂纳米粒子(Pt-NPs)具有抗肿瘤活性,并且能够清除超氧化物和过氧化物,这表明它们可以作为超氧化物歧化酶(SOD)/过氧化氢酶模拟物。这些潜力在保护和/或改善与氧化应激相关的病理方面似乎很有用,但是,当它们与依赖于活性氧在细胞杀伤诱导中的介导的治疗方式结合使用时,Pt-NPs 的效果可能值得怀疑。在这里,研究了聚丙烯酸封端的 Pt-NPs(纳米-Pt)对人髓单核白血病 U937 和人皮肤 T 细胞淋巴瘤 HH 细胞的热疗(HT)诱导细胞凋亡的影响及其潜在的分子机制。结果表明,纳米-Pt 的预处理以剂量依赖的方式显著抑制 HT 诱导的细胞凋亡。超氧化物,但不是过氧化物,受到不同程度的抑制。凋亡执行的所有途径也受到负面影响。结果表明,纳米-Pt 和 HT 的组合可能导致 HT 脱敏。