Involvement of CD73 and A2B Receptor in Radiation-Induced DNA Damage Response and Cell Migration in Human Glioblastoma A172 Cells

نویسندگان

چکیده

Glioblastoma is the most common malignant tumor of central nervous system and treated with a combination surgery, radiation chemotherapy. However, often acquires resistance, which characterized by an increased DNA damage response (DDR). Here, we show that CD73, generates extracellular adenosine from ATP, A2B receptor, activated adenosine, are involved in γ-radiation-induced DDR enhanced migration ability human glioblastoma cell line A172. To investigate DDR, evaluated ataxia telangiectasia mutated (ATM) activation focus formation histone H2A isoform γ (γH2AX) p53-binding protein 1 (53BP1) nucleus A172 cells after γ-irradiation. Antagonists receptor or knockdown small interfering RNA (siRNA), suppressed promoted death, as well suppressing actin remodeling. These results suggest generated via CD73 promotes leading to recovery damage, also enhances The CD73-A2B pathway may be promising target for overcoming resistance acquisition phenotypes during radiotherapy glioblastoma.

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ژورنال

عنوان ژورنال: Biological & Pharmaceutical Bulletin

سال: 2021

ISSN: ['1347-5215', '0918-6158']

DOI: https://doi.org/10.1248/bpb.b20-00654