Hildebrand Laura S, Jost Tina, Schindler Marion, Derer Anja, Fuhrmann Gregor, Fietkau Rainer, Distel Luitpold V
Department of Radiation Oncology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Universitätsstraße 27, 91054, Erlangen, Germany.
Comprehensive Cancer Center Erlangen-EMN (CCC ER-EMN), Erlangen, Germany.
Sci Rep. 2025 May 22;15(1):17871. doi: 10.1038/s41598-025-03159-5.
Radiotherapy (RT) is a relevant treatment for head and neck squamous cell carcinoma (HNSCC) patients but radioresistance, which depends on DNA damage response (DDR), restrains outcome. Therefore, manipulating DDR by small molecule inhibitors (SMI) is a promising treatment option. The main DNA double strand break (DSB) repair mechanisms in healthy mammalian cells are homologous recombination (HR) and non-homologous end joining (NHEJ). It is known that HR is already often impaired in tumors because of cancerous transitions. Therefore, additionally inhibiting NHEJ is a possibility to specifically target tumor cells and spare healthy tissue, which has the alternative DSB repair mechanism available. We treated HNSCC and healthy fibroblast cell lines with 30 µM of the ligase IV inhibitor SCR130 and a single dose of 2 Gy (Gy) ionizing radiation (IR) to investigate the inhibitor's radiosensitizing effect. In short, the effect of SCR130 in combination with IR on cell death, clonogenicity, and DNA damage is limited and highly cell line specific. Nevertheless, SCR130 increases the number of cells in G0/G1 phase concomitant with gained p21 expression consistently. We suggest that SCR130 in combination with IR has anti-proliferative effects, but an escape of the cells by upregulation of ligase IV resulting from the treatment is possible.
放射疗法(RT)是头颈部鳞状细胞癌(HNSCC)患者的一种相关治疗方法,但依赖于DNA损伤反应(DDR)的放射抗性会限制治疗效果。因此,通过小分子抑制剂(SMI)来调控DDR是一种很有前景的治疗选择。健康哺乳动物细胞中主要的DNA双链断裂(DSB)修复机制是同源重组(HR)和非同源末端连接(NHEJ)。已知由于癌变转变,HR在肿瘤中常常已经受损。因此,额外抑制NHEJ有可能特异性地靶向肿瘤细胞并保护具有替代DSB修复机制的健康组织。我们用30µM的连接酶IV抑制剂SCR130和单剂量2戈瑞(Gy)的电离辐射(IR)处理HNSCC和健康成纤维细胞系,以研究该抑制剂的放射增敏作用。简而言之,SCR130与IR联合使用对细胞死亡、克隆形成能力和DNA损伤的影响有限且具有高度细胞系特异性。然而,SCR130持续增加G0/G1期的细胞数量,并伴随着p21表达的增加。我们认为SCR130与IR联合使用具有抗增殖作用,但治疗导致的连接酶IV上调可能使细胞产生逃逸。