Wong Ho Ning, Lewies Angélique, Haigh Michaela, Viljoen Joe M, Wentzel Johannes F, Haynes Richard K, du Plessis Lissinda H
Centre of Excellence for Pharmaceutical Sciences (Pharmacen™), North-West University, Potchefstroom, South Africa.
Front Pharmacol. 2020 Sep 29;11:558894. doi: 10.3389/fphar.2020.558894. eCollection 2020.
The most frequently occurring cancers are those of the skin, with melanoma being the leading cause of death due to skin cancer. Breakthroughs in chemotherapy have been achieved in certain cases, though only marginal advances have been made in treatment of metastatic melanoma. Strategies aimed at inducing redox dysregulation by use of reactive oxygen species (ROS) inducers present a promising approach to cancer chemotherapy. Here we use a rational combination of an oxidant drug combined with a redox or pro-oxidant drug to optimize the cytotoxic effect. Thus we demonstrate for the first time enhanced activity of the amino-artemisinin artemisone and novel prenylated piperazine derivatives derived from dihydroartemisinin as the oxidant component, and elesclomol-Cu(II) as the redox component, against human malignant melanoma cells A375 . The combinations caused a dose dependent decrease in cell numbers and increase in apoptosis. The results indicate that oxidant-redox drug combinations have considerable potential and warrant further investigation.
最常见的癌症是皮肤癌,其中黑色素瘤是皮肤癌致死的主要原因。虽然在某些病例中化疗已取得突破,但在转移性黑色素瘤的治疗方面仅取得了微不足道的进展。通过使用活性氧(ROS)诱导剂来引发氧化还原失调的策略为癌症化疗提供了一种有前景的方法。在此,我们合理组合一种氧化药物与一种氧化还原或促氧化药物,以优化细胞毒性作用。因此,我们首次证明,作为氧化成分的氨基青蒿素青蒿酮和源自二氢青蒿素的新型异戊烯基哌嗪衍生物,以及作为氧化还原成分的依斯氯醇 - 铜(II),对人恶性黑色素瘤细胞A375具有增强的活性。这些组合导致细胞数量呈剂量依赖性减少,并使细胞凋亡增加。结果表明,氧化 - 氧化还原药物组合具有相当大的潜力,值得进一步研究。