Chekkat Neila, Dahm Georges, Chardon Edith, Wantz May, Sitz Justine, Decossas Marion, Lambert Olivier, Frisch Benoit, Rubbiani Riccardo, Gasser Gilles, Guichard Gilles, Fournel Sylvie, Bellemin-Laponnaz Stéphane
Faculté de Pharmacie, Université de Strasbourg-CNRS UMR 7199 , Route du Rhin, BP 60024, 67401 Illkirch cedex, France.
Institut de Physique et Chimie des Matériaux de Strasbourg Université de Strasbourg-CNRS UMR 7504 , 23 rue du Loess, BP 43, 67034 Strasbourg cedex 2, France.
Bioconjug Chem. 2016 Aug 17;27(8):1942-8. doi: 10.1021/acs.bioconjchem.6b00320. Epub 2016 Aug 8.
The current interest for platinum N-heterocyclic carbene complexes in cancer research stems from their impressive toxicity reported against a range of different human cancer cells. To date, the demonstration of their in vivo efficacy relative to that of established platinum-based drugs has not been specifically addressed. Here, we introduce an innovative approach to increase the NHC-Pt complex potency whereby multiple NHC-Pt(II) complexes are coordinated along a polyethylenimine polymer (PEI) chain. We show that such NHC-Pt(II)-PEI conjugates induce human cancer cell death in vitro and in vivo in a xenograft mouse model with no observable side effects in contrast to oxaliplatin. Additional studies indicate nucleus and mitochondria targeting and suggest various mechanisms of action compared to classical platinum-based anticancer drugs.
目前铂氮杂环卡宾配合物在癌症研究中的热度源于其对一系列不同人类癌细胞显示出的显著毒性。迄今为止,相对于已有的铂类药物,其体内疗效尚未得到具体论证。在此,我们引入一种创新方法来提高氮杂环卡宾-铂配合物的效力,即将多个氮杂环卡宾-铂(II)配合物沿聚乙烯亚胺聚合物(PEI)链进行配位。我们发现,与奥沙利铂相比,此类氮杂环卡宾-铂(II)-PEI缀合物在体外和异种移植小鼠模型体内均可诱导人类癌细胞死亡,且未观察到明显副作用。进一步研究表明其具有细胞核和线粒体靶向性,与传统铂类抗癌药物相比,作用机制也有所不同。