Department of Chemistry and Biochemistry, Kent State University, 236 Integrated Sciences Building, Kent, OH 44242, USA.
Department of Chemistry, University of Bisha, Bisha 67714, Saudi Arabia.
Int J Mol Sci. 2023 Aug 27;24(17):13301. doi: 10.3390/ijms241713301.
We conducted the first comprehensive investigation on the impact of head group modifications on the anticancer activities of fatty-acid-like Pt(IV) prodrugs (FALPs), which are a class of platinum-based metallodrugs that target mitochondria. We created a small library of FALPs (-) with diverse head group modifications. The outcomes of our study demonstrate that hydrophilic modifications exclusively enhance the potency of these metallodrugs, whereas hydrophobic modifications significantly decrease their cytotoxicity. To further understand this interesting structure-activity relationship, we chose two representative FALPs (compounds and ) as model compounds: one () with a hydrophilic polyethylene glycol (PEG) head group, and the other () with a hydrophobic hydrocarbon modification of the same molecular weight. Using these FALPs, we conducted a targeted investigation on the mechanism of action. Our study revealed that compound , with hydrophilic modifications, exhibited remarkable penetration into cancer cells and mitochondria, leading to subsequent mitochondrial and DNA damage, and effectively eradicating cancer cells. In contrast, compound , with hydrophobic modifications, displayed a significantly lower uptake and weaker cellular responses. The collective results present a different perspective, indicating that increased hydrophobicity may not necessarily enhance cellular uptake as is conventionally believed. These findings provide valuable new insights into the fundamental principles of developing metallodrugs.
我们首次全面研究了端基修饰对脂肪酸样铂(IV)前药(FALP)抗癌活性的影响,FALP 是一类靶向线粒体的铂基金属药物。我们构建了一个具有不同端基修饰的 FALP(-)小分子库。研究结果表明,亲水修饰可显著提高这些金属药物的效力,而疏水修饰则明显降低其细胞毒性。为了进一步理解这一有趣的构效关系,我们选择了两种代表性的 FALP(化合物 和 )作为模型化合物:一种()具有亲水性聚乙二醇(PEG)端基,另一种()具有相同分子量的疏水性烃修饰。利用这些 FALP,我们针对作用机制进行了靶向研究。我们的研究表明,具有亲水修饰的化合物 显示出显著的穿透癌细胞和线粒体的能力,进而导致线粒体和 DNA 损伤,并有效杀灭癌细胞。相比之下,具有疏水性修饰的化合物 摄取和细胞反应较弱。综合结果提供了一个不同的视角,表明增加疏水性不一定如传统观点所认为的那样能增强细胞摄取。这些发现为开发金属药物的基本原则提供了有价值的新见解。