Faculty of Basic Medicine, M.V. Lomonosov Moscow State University, 27/1 Lomonosovsky Prospekt, Moscow, 119192, Russian Federation.
Federal Research Center: Crystallography and Photonics, Russian Academy of Sciences, Leninsky Prospekt 59, Moscow, 119333, Russian Federation.
Pharm Res. 2017 Jun;34(6):1264-1275. doi: 10.1007/s11095-017-2143-1. Epub 2017 Mar 20.
The effect of existing anti-cancer therapies is based mainly on the stimulation of apoptosis in cancer cells. Here, we have demonstrated the ability of a catalytically-reactive nanoparticle-based complex of cytochrome c with cardiolipin (Cyt-CL) to induce the apoptosis and killing of cancer cells in a monolayer cell culture.
Cyt-CL nanoparticles were prepared by complexing CytC with different molar excesses of CL. Following characterization, cytotoxicity and apoptosis inducing effects of nanoparticles were investigated. In an attempt to identify the anticancer activity mechanism of Cyt-CL, pseudo-lipoxygenase and lipoperoxidase reaction kinetics were measured by chemiluminescence.
Using chemiluminescence, we have demonstrated that the Cyt-CL complex produces lipoperoxide radicals in two reactions: by decomposition of lipid hydroperoxides, and by lipid peroxidation under the action of HO. Antioxidants inhibited the formation of lipid radicals. Cyt-CL nanoparticles, but not the CytC alone, dramatically enhanced the level of apoptosis and cell death in two cell lines: drug-sensitive (A2780) and doxorubicin-resistant (A2780-Adr). The proposed mechanism of the cytotoxic action of Cyt-CL involves either penetration through the cytoplasm and outer mitochondrial membrane and catalysis of lipid peroxidation reactions at the inner mitochondrial membrane, or/and activation of lipid peroxidation within the cytoplasmic membrane.
Here we propose a new type of anticancer nano-formulation, with an action based on the catalytic action of Cyt-CL nanoparticles on the cell membrane and and/or mitochondrial membranes that results in lipid peroxidation reactions, which give rise to activation of apoptosis in cancer cells, including multidrug resistant cells.
现有的抗癌疗法的效果主要基于刺激癌细胞凋亡。在这里,我们已经证明了细胞色素 c 与心磷脂(Cyt-CL)的催化反应纳米颗粒复合物在单层细胞培养中诱导癌细胞凋亡和杀伤的能力。
通过用不同摩尔过量的 CL 与 CytC 复合来制备 Cyt-CL 纳米颗粒。对纳米颗粒的细胞毒性和诱导凋亡作用进行了表征。为了确定 Cyt-CL 的抗癌活性机制,通过化学发光法测量了伪脂氧合酶和脂过氧化酶反应动力学。
使用化学发光法,我们已经证明 Cyt-CL 复合物在两个反应中产生活性氧自由基:通过分解脂质氢过氧化物和在 HO 作用下的脂质过氧化。抗氧化剂抑制了脂质自由基的形成。Cyt-CL 纳米颗粒,但不是 CytC 本身,在两种细胞系(敏感(A2780)和阿霉素耐药(A2780-Adr))中显著增强了细胞凋亡和细胞死亡的水平。Cyt-CL 细胞毒性作用的提出机制涉及穿过细胞质和外线粒体膜的穿透和/或在内线粒体膜上催化脂质过氧化反应,或/和在细胞质膜内激活脂质过氧化。
在这里,我们提出了一种新型的抗癌纳米制剂,其作用基于 Cyt-CL 纳米颗粒在细胞膜和/或线粒体膜上的催化作用,导致脂质过氧化反应,从而激活癌细胞,包括多药耐药细胞的凋亡。