Department of Chinese Medicine Oncology, The First Affiliated Hospital of Naval Medical University, Shanghai, People's Republic of China.
Department of Chinese Medicine, Naval Medical University, Shanghai, People's Republic of China.
Int J Nanomedicine. 2024 May 28;19:4803-4834. doi: 10.2147/IJN.S461289. eCollection 2024.
The utilization of PD-1/PD-L1 inhibitors marks a significant advancement in cancer therapy. However, the efficacy of monotherapy is still disappointing in a substantial subset of patients, necessitating the exploration of combinational strategies. Emerging from the promising results of the KEYNOTE-942 trial, RNA-based therapies, particularly circRNAs and piRNAs, have distinguished themselves as innovative sensitizers to immune checkpoint inhibitors (ICIs). These non-coding RNAs, notable for their stability and specificity, were once underrecognized but are now known for their crucial roles in regulating PD-L1 expression and bolstering anti-cancer immunity. Our manuscript offers a comprehensive analysis of selected circRNAs and piRNAs, elucidating their immunomodulatory effects and mechanisms, thus underscoring their potential as ICIs enhancers. In conjunction with the recent Nobel Prize-awarded advancements in mRNA vaccine technology, our review highlights the transformative implications of these findings for cancer treatment. We also discuss the prospects of circRNAs and piRNAs in future therapeutic applications and research. This study pioneers the synergistic application of circRNAs and piRNAs as novel sensitizers to augment PD-1/PD-L1 inhibition therapy, demonstrating their unique roles in regulating PD-L1 expression and modulating immune responses. Our findings offer a groundbreaking approach for enhancing the efficacy of cancer immunotherapy, opening new avenues for treatment strategies. This abstract aims to encapsulate the essence of our research and the burgeoning role of these non-coding RNAs in enhancing PD-1/PD-L1 inhibition therapy, encouraging further investigation into this promising field.
PD-1/PD-L1 抑制剂的应用标志着癌症治疗的重大进展。然而,在相当一部分患者中,单药治疗的疗效仍然令人失望,因此需要探索联合治疗策略。从 KEYNOTE-942 试验的有希望的结果中涌现出的 RNA 疗法,特别是 circRNAs 和 piRNAs,作为免疫检查点抑制剂(ICIs)的创新增敏剂脱颖而出。这些非编码 RNA 以其稳定性和特异性为特征,曾经被低估,但现在已知它们在调节 PD-L1 表达和增强抗癌免疫方面发挥着关键作用。我们的论文对选定的 circRNAs 和 piRNAs 进行了全面分析,阐明了它们的免疫调节作用和机制,从而强调了它们作为 ICI 增强剂的潜力。结合最近因 mRNA 疫苗技术而获得诺贝尔奖的进展,我们的综述强调了这些发现对癌症治疗的变革性影响。我们还讨论了 circRNAs 和 piRNAs 在未来治疗应用和研究中的前景。这项研究开创了 circRNAs 和 piRNAs 作为新型增敏剂协同应用的先河,以增强 PD-1/PD-L1 抑制治疗的疗效,展示了它们在调节 PD-L1 表达和调节免疫反应方面的独特作用。我们的研究结果为增强癌症免疫治疗的疗效提供了一种开创性的方法,为治疗策略开辟了新的途径。本摘要旨在概括我们研究的本质以及这些非编码 RNA 在增强 PD-1/PD-L1 抑制治疗中的新兴作用,鼓励进一步研究这一有前途的领域。