Department of Radiation Oncology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.
Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), 91054 Erlangen, Germany.
Genes (Basel). 2021 Jun 17;12(6):925. doi: 10.3390/genes12060925.
(1) Kinase inhibitors (KI) targeting components of the DNA damage repair pathway are a promising new type of drug. Combining them with ionizing radiation therapy (IR), which is commonly used for treatment of head and neck tumors, could improve tumor control, but could also increase negative side effects on surrounding normal tissue. (2) The effect of KI of the DDR (ATMi: AZD0156; ATRi: VE-822, dual DNA-PKi/mTORi: CC-115) in combination with IR on HPV-positive and HPV-negative HNSCC and healthy skin cells was analyzed. Cell death and cell cycle arrest were determined using flow cytometry. Additionally, clonogenic survival and migration were analyzed. (3) Studied HNSCC cell lines reacted differently to DDRi. An increase in cell death for all of the malignant cells could be observed when combining IR and KI. Healthy fibroblasts were not affected by simultaneous treatment. Migration was partially impaired. Influence on the cell cycle varied between the cell lines and inhibitors; (4) In conclusion, a combination of DDRi with IR could be feasible for patients with HNSCC. Side effects on healthy cells are expected to be limited to normal radiation-induced response. Formation of metastases could be decreased because cell migration is impaired partially. The treatment outcome for HPV-negative tumors tends to be improved by combined treatment.
(1)靶向 DNA 损伤修复途径的激酶抑制剂(KI)是一种很有前途的新型药物。将它们与常用于治疗头颈部肿瘤的电离辐射治疗(IR)相结合,可能会提高肿瘤控制效果,但也会增加对周围正常组织的负面副作用。(2)分析了 DDR 的 KI(ATMi:AZD0156;ATR 抑制剂:VE-822,双重 DNA-PKi/mTORi:CC-115)与 IR 联合应用于 HPV 阳性和 HPV 阴性头颈部鳞状细胞癌和健康皮肤细胞的效果。通过流式细胞术测定细胞死亡和细胞周期停滞。此外,还分析了集落形成存活和迁移。(3)研究的头颈部鳞状细胞癌细胞系对 DDRi 的反应不同。当将 IR 和 KI 联合使用时,可以观察到所有恶性细胞的细胞死亡增加。同时处理对健康成纤维细胞没有影响。迁移部分受损。细胞周期的影响在细胞系和抑制剂之间有所不同;(4)总之,DDRi 与 IR 的联合治疗对头颈部鳞状细胞癌患者可能是可行的。对健康细胞的副作用预计仅限于正常的辐射诱导反应。由于部分抑制了细胞迁移,转移的形成可能会减少。联合治疗可改善 HPV 阴性肿瘤的治疗效果。