Division of Radiation Oncology, National Cancer Centre Singapore, 11 Hospital Crescent, 169610, Singapore.
Cancer Science Institute, Yong Loo Lin School of Medicine, National University of Singapore, 117599, Singapore.
Cancer Lett. 2021 Jul 28;511:56-67. doi: 10.1016/j.canlet.2021.04.019. Epub 2021 Apr 29.
Despite numerous advances in cancer radiotherapy, tumor radioresistance remain one of the major challenges limiting treatment efficacy of radiotherapy. Conventional strategies to overcome radioresistance involve understanding the underpinning molecular mechanisms, and subsequently using combinatorial treatment strategies involving radiation and targeted drug combinations against these radioresistant tumors. These strategies exploit and target the molecular fingerprint and vulnerability of the radioresistant clones to achieve improved efficacy in tumor eradication. However, conventional drug-screening approaches for the discovery of new drug combinations have been proven to be inefficient, limited and laborious. With the increasing availability of computational resources in recent years, novel approaches such as Quadratic Phenotypic Optimization Platform (QPOP), CURATE.AI and Drug Combination and Prediction and Testing (DCPT) platform have emerged to aid in drug combination discovery and the longitudinally optimized modulation of combination therapy dosing. These platforms could overcome the limitations of conventional screening approaches, thereby facilitating the discovery of more optimal drug combinations to improve the therapeutic ratio of combinatorial treatment. The use of better and more accurate models and methods with rapid turnover can thus facilitate a rapid translation in the clinic, hence, resulting in a better patient outcome. Here, we reviewed the clinical observations, molecular mechanisms and proposed treatment strategies for tumor radioresistance and discussed how novel approaches may be applied to enhance drug combination discovery, with the aim to further improve the therapeutic ratio and treatment efficacy of radiotherapy against radioresistant cancers.
尽管癌症放射治疗取得了许多进展,但肿瘤放射抵抗仍然是限制放射治疗疗效的主要挑战之一。克服放射抵抗的传统策略包括了解潜在的分子机制,随后使用联合治疗策略,包括放射治疗和针对这些放射抵抗肿瘤的靶向药物联合治疗。这些策略利用并针对放射抵抗克隆的分子指纹和脆弱性,以实现肿瘤清除的疗效提高。然而,用于发现新药物组合的传统药物筛选方法已被证明效率低下、有限且费力。近年来,随着计算资源的日益丰富,出现了新的方法,如二次表型优化平台 (QPOP)、CURATE.AI 和药物组合与预测和测试 (DCPT) 平台,以辅助药物组合发现和联合治疗剂量的纵向优化调节。这些平台可以克服传统筛选方法的局限性,从而促进发现更优化的药物组合,以提高联合治疗的治疗比。因此,使用更好、更准确且具有快速周转的模型和方法可以促进临床快速转化,从而为患者带来更好的治疗效果。在这里,我们回顾了肿瘤放射抵抗的临床观察、分子机制和提出的治疗策略,并讨论了如何应用新方法来增强药物组合发现,以进一步提高放射抵抗癌症的放射治疗治疗比和疗效。