| Literature DB >> 32990677 |
Katherine Deland1, Bryce F Starr1, Joshua S Mercer1, Jovita Byemerwa2, Donna M Crabtree3, Nerissa T Williams1, Lixia Luo1, Yan Ma1, Mark Chen2,4, Oren J Becher5,6,7, David G Kirsch1,2.
Abstract
Diffuse intrinsic pontine glioma (DIPG) kills more children than any other type of brain tumor. Despite clinical trials testing many chemotherapeutic agents, palliative radiotherapy remains the standard treatment. Here, we utilized Cre/loxP technology to show that deleting Ataxia telangiectasia mutated (Atm) in primary mouse models of DIPG can enhance tumor radiosensitivity. Genetic deletion of Atm improved survival of mice with p53-deficient but not p53 wild-type gliomas after radiotherapy. Similar to patients with DIPG, mice with p53 wild-type tumors had improved survival after radiotherapy independent of Atm deletion. Primary p53 wild-type tumor cell lines induced proapoptotic genes after radiation and repressed the NRF2 target, NAD(P)H quinone dehydrogenase 1 (Nqo1). Tumors lacking p53 and Ink4a/Arf expressed the highest level of Nqo1 and were most resistant to radiation, but deletion of Atm enhanced the radiation response. These results suggest that tumor genotype may determine whether inhibition of ATM during radiotherapy will be an effective clinical approach to treat DIPGs.Entities:
Keywords: Brain cancer; Mouse models; Oncology; P53
Year: 2021 PMID: 32990677 PMCID: PMC7773366 DOI: 10.1172/JCI142158
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808