Li Wenhuan, Ji Teng, Ye Jiaqi, Xiong Shengfeng, Si Yao, Sun Xiaohui, Li Fei, Dai Zhoutong
Department of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430034, China.
National Clinical Research Centre for Obstetrics and Gynecology, Cancer Biology Research Centre (Key Laboratory of the Ministry of Education), Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430034, China.
Cancer Gene Ther. 2025 Apr;32(4):403-417. doi: 10.1038/s41417-025-00882-z. Epub 2025 Mar 3.
Oncolytic virotherapy has emerged as a promising strategy for cancer treatment by selectively targeting and lysing tumor cells. However, its efficacy is often limited in certain tumor types due to multiple factors. This study explores the combination of oncolytic adenoviruses with Erastin, a potent ferroptosis inducer, to enhance antitumor efficacy in oncolytic virus-insensitive cancer cell lines. In vitro experiments demonstrated that Erastin significantly increased the cytotoxicity of oncolytic virotherapy, leading to greater inhibition of cell proliferation and elevated rates of cell death compared to monotherapies. The combination treatment further promoted ferroptosis, as evidenced by increased reactive oxygen species (ROS) levels, enhanced lipid peroxidation, and disrupted redox homeostasis. RNA sequencing identified the downregulation of Dickkopf-1 (DKK1) as a key mediator of the enhanced ferroptotic effect. Restoring the expression of DKK1 partially mitigated the cytotoxic effects of the combination therapy, highlighting its crucial role in mediating the enhanced ferroptosis-induced oncolytic virotherapy efficacy. In vivo studies further validated these findings, demonstrating that the combined treatment significantly reduced tumor growth without inducing notable toxicity. This novel therapeutic approach has great potential to enhance the efficacy of oncolytic virotherapy in cancers resistant to oncolytic viruses by inducing ferroptosis. Further investigation in clinically relevant models is warranted to fully elucidate the underlying mechanisms and to optimize this combination strategy for potential clinical applications.
溶瘤病毒疗法已成为一种有前景的癌症治疗策略,可通过选择性靶向并裂解肿瘤细胞来发挥作用。然而,由于多种因素,其疗效在某些肿瘤类型中往往受到限制。本研究探索了溶瘤腺病毒与强效铁死亡诱导剂艾拉斯汀(Erastin)的联合应用,以增强对溶瘤病毒不敏感的癌细胞系的抗肿瘤疗效。体外实验表明,与单一疗法相比,艾拉斯汀显著提高了溶瘤病毒疗法的细胞毒性,导致对细胞增殖的抑制作用更强,细胞死亡率更高。联合治疗进一步促进了铁死亡,表现为活性氧(ROS)水平升高、脂质过氧化增强以及氧化还原稳态破坏。RNA测序确定Dickkopf-1(DKK1)的下调是增强铁死亡效应的关键介质。恢复DKK1的表达部分减轻了联合治疗的细胞毒性作用,突出了其在介导增强的铁死亡诱导的溶瘤病毒疗法疗效中的关键作用。体内研究进一步验证了这些发现,表明联合治疗显著降低了肿瘤生长,且未诱导明显的毒性。这种新型治疗方法具有巨大潜力,可通过诱导铁死亡来增强溶瘤病毒疗法对溶瘤病毒耐药癌症的疗效。有必要在临床相关模型中进行进一步研究,以充分阐明潜在机制,并优化这种联合策略以用于潜在的临床应用。