Gallez Bernard
Biomedical Magnetic Resonance Research Group, Louvain Drug Research Institute, Université Catholique de Louvain (UCLouvain), Brussels, Belgium.
Front Pharmacol. 2022 Jul 15;13:853568. doi: 10.3389/fphar.2022.853568. eCollection 2022.
Hypoxia is a common feature of solid tumors that contributes to angiogenesis, invasiveness, metastasis, altered metabolism and genomic instability. As hypoxia is a major actor in tumor progression and resistance to radiotherapy, chemotherapy and immunotherapy, multiple approaches have emerged to target tumor hypoxia. It includes among others pharmacological interventions designed to alleviate tumor hypoxia at the time of radiation therapy, prodrugs that are selectively activated in hypoxic cells or inhibitors of molecular targets involved in hypoxic cell survival (i.e., hypoxia inducible factors HIFs, PI3K/AKT/mTOR pathway, unfolded protein response). While numerous strategies were successful in pre-clinical models, their translation in the clinical practice has been disappointing so far. This therapeutic failure often results from the absence of appropriate stratification of patients that could benefit from targeted interventions. Companion diagnostics may help at different levels of the research and development, and in matching a patient to a specific intervention targeting hypoxia. In this review, we discuss the relative merits of the existing hypoxia biomarkers, their current status and the challenges for their future validation as companion diagnostics adapted to the nature of the intervention.
缺氧是实体瘤的一个常见特征,它会促进血管生成、侵袭、转移、代谢改变和基因组不稳定。由于缺氧是肿瘤进展以及对放疗、化疗和免疫治疗产生抗性的主要因素,因此已经出现了多种针对肿瘤缺氧的方法。其中包括旨在在放射治疗时缓解肿瘤缺氧的药物干预、在缺氧细胞中被选择性激活的前体药物或参与缺氧细胞存活的分子靶点抑制剂(即缺氧诱导因子HIFs、PI3K/AKT/mTOR通路、未折叠蛋白反应)。虽然许多策略在临床前模型中取得了成功,但到目前为止,它们在临床实践中的转化效果并不理想。这种治疗失败往往是由于缺乏对可能从靶向干预中受益的患者进行适当分层。伴随诊断可能在研发的不同阶段有所帮助,并有助于将患者与针对缺氧的特定干预措施相匹配。在这篇综述中,我们讨论了现有缺氧生物标志物的相对优点、它们的现状以及未来作为适应干预性质伴随诊断进行验证所面临的挑战。