Ontology highlight
ABSTRACT: Background
Head and neck squamous cell carcinoma (HNSCC) negative for Human Papillomavirus (HPV) has remained a difficult to treat entity, whereas tumors positive for HPV are characterized by radiosensitivity and favorable patient outcome. On the cellular level, radiosensitivity is largely governed by the tumor cells` ability to repair radiation-induced DNA double-strand breaks (DSBs), but no biomarker is established that could guide clinical decision making. Therefore, we tested the impact of the expression levels of ATM, the central kinase of the DNA damage response as well as DNA-PKcs and Ku80, two major factors in the main DSB repair pathway non-homologous end joining (NHEJ).Methods
A tissue microarray of a single center HNSCC cohort was stained for ATM, DNA-PKcs and Ku
SUBMITTER: Zech HB
PROVIDER: S-EPMC11523811 | biostudies-literature | 2024 Oct
REPOSITORIES: biostudies-literature