Zhang Cheng, Kang Tong, Wang Xinyi, Song Jiaqi, Zhang Jia, Li Guanying
The Department of Thoracic Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Front Pharmacol. 2022 Oct 17;13:1035217. doi: 10.3389/fphar.2022.1035217. eCollection 2022.
Lung cancer is the most common cause of cancer-related deaths worldwide. More efficient treatments are desperately needed. For decades, the success of platinum-based anticancer drugs has promoted the exploration of metal-based agents. Four ruthenium-based complexes have also entered clinical trials as candidates of anticancer metallodrugs. However, systemic toxicity, severe side effects and drug-resistance impeded their applications and efficacy. Stimuli-responsiveness of Pt- and Ru-based complexes provide a great chance to weaken the side effects and strengthen the clinical efficacy in drug design. This review provides an overview on the stimuli-responsive Pt- and Ru-based metallic anticancer drugs for lung cancer. They are categorized as endo-stimuli-responsive, exo-stimuli-responsive, and dual-stimuli-responsive prodrugs based on the nature of stimuli. We describe various representative examples of structure, response mechanism, and potential medical applications in lung cancer. In the end, we discuss the future opportunities and challenges in this field.
肺癌是全球癌症相关死亡的最常见原因。迫切需要更有效的治疗方法。几十年来,铂类抗癌药物的成功推动了金属基药物的探索。四种钌基配合物也已作为抗癌金属药物的候选物进入临床试验。然而,全身毒性、严重的副作用和耐药性阻碍了它们的应用和疗效。基于铂和钌的配合物的刺激响应性为在药物设计中减弱副作用和增强临床疗效提供了很大的机会。本综述概述了用于肺癌的刺激响应性铂基和钌基金属抗癌药物。根据刺激的性质,它们被分类为内刺激响应性、外刺激响应性和双刺激响应性前药。我们描述了结构、响应机制和在肺癌中的潜在医学应用的各种代表性实例。最后,我们讨论了该领域未来的机遇和挑战。