Azuaje Francisco, Tiemann Katja, Niclou Simone P
Department of Oncology, NorLux Neuro-Oncology Laboratory, Luxembourg Institute of Health (LIH), Luxembourg, Luxembourg.
Cell Commun Signal. 2015 Mar 31;13:23. doi: 10.1186/s12964-015-0098-6.
The alteration of the epidermal growth factor receptor (EGFR)-driven signaling network is a characteristic feature of glioblastomas (GBM), and its inhibition represents a treatment strategy. However, EGFR-targeted interventions have been largely ineffective. Complex perturbations in this system are likely to be central to tumor cells with high adaptive capacity and resistance to therapies. We review key concepts and mechanisms relevant to EGFR-targeted treatment resistance at a systems level. Our understanding of treatment resistance as a systems-level phenomenon is necessary to develop effective therapeutic options for GBM patients. This is allowing us to go beyond the notion of therapeutic targets as single molecular components, into strategies that can weaken cancer signaling robustness and boost inherent network-level vulnerabilities.
表皮生长因子受体(EGFR)驱动的信号网络改变是胶质母细胞瘤(GBM)的一个特征性表现,对其进行抑制是一种治疗策略。然而,针对EGFR的干预措施在很大程度上并不奏效。该系统中的复杂扰动可能是具有高适应能力和抗治疗性的肿瘤细胞的核心问题。我们在系统层面回顾了与EGFR靶向治疗耐药性相关的关键概念和机制。将治疗耐药性理解为一种系统层面的现象,对于为GBM患者开发有效的治疗方案是必要的。这使我们能够超越将治疗靶点视为单一分子成分的概念,转向能够削弱癌症信号稳健性并增强内在网络层面脆弱性的策略。