Sánchez-Pérez Isabel
Instituto de Investigaciones Biomédicas del CSIC/UAM, Traslational Oncology Unit CSIC/Hospital La Paz, Madrid, Spain.
Clin Transl Oncol. 2006 Sep;8(9):642-6. doi: 10.1007/s12094-006-0034-8.
Chemotherapy and radiation are two important modalities for cancer treatment. Many agents in clinical used have the ability to induce DNA damage, however they may be highly cytotoxic as a secondary effect. Different mechanisms are involved both, in detection and repair of DNA damage. The modulation of these pathways, has a great impact on clinical outcome and is frequently responsible of therapeutic resistance. Therefore, pharmacological inhibition of DNA damage repair pathways has been explored as a useful strategy to enhance chemo and radiosensitivity, thus it could be used for reversing drug resistance. Different agents have shown excellent results in preclinical studies in combination with radiation or chemotherapy. Early phase clinical trials are now being carried out using different DNA repair inhibitors targeting several enzymes such as PARP, DNA-PK or MGMT.
化疗和放疗是癌症治疗的两种重要方式。临床使用的许多药物都有诱导DNA损伤的能力,然而它们可能会产生高度细胞毒性的副作用。DNA损伤的检测和修复涉及不同的机制。这些途径的调节对临床结果有很大影响,并且常常是治疗耐药性的原因。因此,探索DNA损伤修复途径的药理学抑制作为增强化疗和放射敏感性的有用策略,从而可用于逆转耐药性。不同的药物在与放疗或化疗联合的临床前研究中已显示出优异的结果。目前正在进行早期临床试验,使用针对几种酶如PARP、DNA-PK或MGMT的不同DNA修复抑制剂。