Yang Gang-Gang, Su Xu-Xian, Liang Bing-Bing, Pan Zheng-Yin, Cao Qian, Mao Zong-Wan
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University Guangzhou 510275 P. R. China
School of Chemistry and Chemical Engineering, Anhui University of Technology Ma'anshan Anhui 243002 P. R. China.
Chem Sci. 2022 Sep 9;13(38):11360-11367. doi: 10.1039/d2sc03375e. eCollection 2022 Oct 5.
Regulation of tumor hypoxia and redox homeostasis is a promising strategy for cancer therapy. Nanocatalytic medicine has played more and more important roles in this field because it can cleverly convert the efficiency and selectivity of catalysis into high therapeutic efficiency. Herein, we developed a platinum(iv)-ruthenium hybrid prodrug, named as Pt-Ru, for efficient chemo-catalytic synergistic therapy of hypoxic tumors. The ruthenium hybridization endowed the Pt(iv) prodrug with multi-enzyme catalytic activity, that is, mimicking catalase (CAT) to generate O , mimicking peroxidase (POD) to produce reactive oxygen species, and mimicking glutathione peroxidase (GPx) to deplete GSH, thus effectively overcoming tumor hypoxia and cisplatin resistance. As a result, Pt-Ru treatment led to a superior anticancer efficacy to cisplatin both and . This work suggested redox homeostasis regulation as a tantalizing angle for developing the next generation of platinum drugs.
调节肿瘤缺氧和氧化还原稳态是一种很有前景的癌症治疗策略。纳米催化药物在该领域发挥着越来越重要的作用,因为它可以巧妙地将催化效率和选择性转化为高治疗效果。在此,我们开发了一种铂(IV)-钌混合前药,命名为Pt-Ru,用于对缺氧肿瘤进行高效化学催化协同治疗。钌杂化赋予了铂(IV)前药多酶催化活性,即模拟过氧化氢酶(CAT)产生O,模拟过氧化物酶(POD)产生活性氧,模拟谷胱甘肽过氧化物酶(GPx)消耗谷胱甘肽,从而有效克服肿瘤缺氧和顺铂耐药性。因此,Pt-Ru治疗在体内和体外均产生了优于顺铂的抗癌效果。这项工作表明氧化还原稳态调节是开发下一代铂类药物的一个诱人角度。