Haasler Lisa, Kondadi Arun Kumar, Tsigaras Thanos, von Montfort Claudia, Graf Peter, Stahl Wilhelm, Brenneisen Peter
Institute of Biochemistry and Molecular Biology I, Medical Faculty, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.
Arch Toxicol. 2021 Apr;95(4):1349-1365. doi: 10.1007/s00204-021-02987-4. Epub 2021 Feb 1.
A major challenge in current cancer therapy is still the treatment of metastatic melanomas of the skin. BH3 mimetics represent a novel group of substances inducing apoptosis. In this study, we investigated the cytotoxic effect of (±) gossypol (GP), a natural compound from cotton seed, on A375 melanoma cells and the underlying biochemical mechanisms. To prevent undesired side effects due to toxicity on normal (healthy) cells, concentrations only toxic for tumor cells have been elaborated. Viability assays were performed to determine the cytotoxicity of GP in A375 melanoma and normal (healthy) cells. For the majority of experiments, a concentration of 2.5 µM GP was used resulting in a ROS-independent but caspase-dependent cell death of A375 melanoma cells. At this level, GP was non-toxic for normal human epidermal melanocytes. GP has a very short half-life, however, it was demonstrated that only the "parent" compound and not decomposition products are responsible for the cytotoxic effect in A375 melanoma cells. GP significantly decreased mitochondrial membrane potential accompanied by a Drp1-dependent loss of mitochondrial integrity (fragmentation) in tumor cells. Taken together, GP induced a ROS-independent intrinsic apoptosis leading to the conclusion that within a specific concentration range, GP may work as effective anticancer drug without harmful side effects.
当前癌症治疗中的一个主要挑战仍然是皮肤转移性黑色素瘤的治疗。BH3模拟物代表了一类新型的诱导细胞凋亡的物质。在本研究中,我们研究了棉籽中的天然化合物(±)棉酚(GP)对A375黑色素瘤细胞的细胞毒性作用及其潜在的生化机制。为了防止由于对正常(健康)细胞的毒性而产生的不良副作用,已确定了仅对肿瘤细胞有毒的浓度。进行了活力测定以确定GP对A375黑色素瘤细胞和正常(健康)细胞的细胞毒性。在大多数实验中,使用2.5 μM的GP浓度,导致A375黑色素瘤细胞发生不依赖活性氧(ROS)但依赖半胱天冬酶的细胞死亡。在此浓度下,GP对正常人表皮黑素细胞无毒。GP的半衰期很短,然而,已证明只有“母体”化合物而非分解产物对A375黑色素瘤细胞的细胞毒性作用负责。GP显著降低了线粒体膜电位,并伴随着肿瘤细胞中线粒体完整性(碎片化)的Drp1依赖性丧失。综上所述,GP诱导了不依赖ROS的内源性凋亡,从而得出结论,在特定浓度范围内,GP可能作为有效的抗癌药物而无有害副作用。