Department of Medical Biology, Faculty of Medicine, Istinye University, Istanbul 34010, Turkey.
Molecular Cancer Research Laboratory (ISUMCRC), Istinye University, Istanbul 34010, Turkey.
Cells. 2022 Apr 26;11(9):1463. doi: 10.3390/cells11091463.
Cholangiocarcinoma (CCA) is a poorly treatable type of cancer and its incidence is dramatically increasing. The lack of understanding of the biology of this tumor has slowed down the identification of novel targets and the development of effective treatments. Based on next generation sequencing profiling, alterations in DNA damage response (DDR)-related genes are paving the way for DDR-targeting strategies in CCA. Based on the notion of synthetic lethality, several DDR-inhibitors (DDRi) have been developed with the aim of accumulating enough DNA damage to induce cell death in tumor cells. Observing that DDRi alone could be insufficient for clinical use in CCA patients, the combination of DNA-damaging regimens with targeted approaches has started to be considered, as evidenced by many emerging clinical trials. Hence, novel therapeutic strategies combining DDRi with patient-specific targeted drugs could be the next level for treating cholangiocarcinoma.
胆管癌(CCA)是一种难以治疗的癌症,其发病率正在显著上升。由于对这种肿瘤生物学的了解不足,新型靶点的鉴定和有效治疗方法的开发速度也有所放缓。基于下一代测序分析,DNA 损伤反应(DDR)相关基因的改变为 CCA 的 DDR 靶向策略铺平了道路。基于合成致死的概念,已经开发了几种 DDR 抑制剂(DDRi),旨在积累足够的 DNA 损伤,以诱导肿瘤细胞死亡。观察到 DDRi 单独用于 CCA 患者的临床应用可能还不够,因此已经开始考虑将 DNA 损伤方案与靶向方法相结合,许多新的临床试验为此提供了证据。因此,将 DDRi 与针对患者的靶向药物相结合的新型治疗策略可能是治疗胆管癌的下一个层次。