de Roest Reinout H, Buijze Marijke, Veth Myrthe, de Lint Klaas, Pai Govind, Rooimans Martin A, Wolthuis Rob M F, Brink Arjen, Poell Jos B, Brakenhoff Ruud H
Amsterdam UMC location VUmc Amsterdam, Otolaryngology/Head and Neck Surgery, Head and Neck Cancer Biology and Immunology laboratory, Amsterdam, The Netherlands.
Cancer Center Amsterdam, Cancer Biology and Immunology, Amsterdam, The Netherlands.
PLoS One. 2025 Aug 6;20(8):e0329731. doi: 10.1371/journal.pone.0329731. eCollection 2025.
Radiotherapy is a mainstay of treatment for head and neck squamous cell carcinoma (HNSCC), either definitive or adjuvant to surgery. Biological factors known to affect radiation response are hypoxia and DNA repair capacity, but several lines of evidence indicate that other genes and pathways in the tumor cells might be involved that have not been elucidated. Here, we report the results of a genome-wide CRISPR-Cas9 functional genomics screen in HNSCC cells to identify radiosensitizing genes. Remarkably, microtubule organizing genes were identified with CLASP1 as most unexpected radiosensitizing hit. Clonogenic assay confirmed the radiosensitizing effect of CLASP1 knockout. Functional analysis showed that CLASP1 knockout has major impact during S-phase, and resulted in mitotic cells with broken chromosomes and cell death. CLASP1 and possibly the microtubule machinery in broader sense seem involved in protection of HNSCC cells against radiation-induced DNA damage. This newly identified mechanism provides an outlook for novel treatment approaches in HNSCC.
放射治疗是头颈部鳞状细胞癌(HNSCC)治疗的主要手段,可作为根治性治疗或手术辅助治疗。已知影响放射反应的生物学因素有缺氧和DNA修复能力,但有几条证据表明肿瘤细胞中的其他基因和信号通路可能也参与其中,只是尚未阐明。在此,我们报告了在HNSCC细胞中进行全基因组CRISPR-Cas9功能基因组学筛选以鉴定放射增敏基因的结果。值得注意的是,鉴定出了微管组织基因,其中CLASP1是最出人意料的放射增敏靶点。克隆形成试验证实了CLASP1基因敲除的放射增敏作用。功能分析表明,CLASP1基因敲除在S期有重大影响,并导致有染色体断裂的有丝分裂细胞和细胞死亡。CLASP1以及广义上可能的微管机制似乎参与保护HNSCC细胞免受辐射诱导的DNA损伤。这一新发现的机制为HNSCC的新型治疗方法提供了前景。