Meerz Annina, Deville Sara Sofia, Müller Johannes, Cordes Nils
OncoRay-National Center for Radiation Research in Oncology, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany.
Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Institute of Radiooncology-OncoRay, 01328 Dresden, Germany.
Cancers (Basel). 2021 Mar 10;13(6):1190. doi: 10.3390/cancers13061190.
For better tumor control, high-precision proton beam radiation therapy is currently being intensively discussed relative to conventional photon therapy. Here, we assumed that radiation type-specific molecular response profiles in more physiological 3D, matrix-based head and neck squamous cell carcinoma (HNSCC) cell cultures can be identified and therapeutically exploited. While proton irradiation revealed superimposable clonogenic survival and residual DNA double strand breaks (DSB) relative to photon irradiation, kinome profiles showed quantitative differences between both irradiation types. Pharmacological inhibition of a subset of radiation-induced kinases, predominantly belonging to the mitogen-activated protein kinase (MAPK) family, failed to sensitize HNSCC cells to either proton or photon irradiation. Likewise, inhibitors for ATM, DNA-PK and PARP did not discriminate between proton and photon irradiation but generally elicited a radiosensitization. Conclusively, our results suggest marginal cell line-specific differences in the radiosensitivity and DSB repair without a superiority of one radiation type over the other in 3D grown HNSCC cell cultures. Importantly, radiation-induced activity changes of cytoplasmic kinases induced during the first, acute phase of the cellular radiation response could neither be exploited for sensitization of HNSCC cells to photon nor proton irradiation.
为了更好地控制肿瘤,目前正在深入讨论相对于传统光子疗法的高精度质子束放射治疗。在此,我们假设在更接近生理状态的基于三维基质的头颈部鳞状细胞癌(HNSCC)细胞培养物中,可以识别出辐射类型特异性分子反应谱并加以治疗应用。虽然相对于光子照射,质子照射显示出可叠加的克隆形成存活率和残留DNA双链断裂(DSB),但激酶组谱显示两种照射类型之间存在定量差异。对一部分主要属于丝裂原活化蛋白激酶(MAPK)家族的辐射诱导激酶进行药理抑制,未能使HNSCC细胞对质子或光子照射敏感。同样,ATM、DNA-PK和PARP的抑制剂在质子和光子照射之间没有差异,但总体上引起了放射增敏作用。总之,我们的结果表明,在三维培养的HNSCC细胞培养物中,细胞系特异性的放射敏感性和DSB修复差异很小,且一种辐射类型并不优于另一种。重要的是,在细胞辐射反应的第一个急性期诱导的细胞质激酶的辐射诱导活性变化,既不能用于使HNSCC细胞对光子照射敏感,也不能用于使HNSCC细胞对质子照射敏感。