Defining the role of Tip60 in the DNA damage response of glioma cell lines.

ATM DNA repair DNA-PK Rad51 Tip60 chromatrin structure

Journal

International journal of radiation biology
ISSN: 1362-3095
Titre abrégé: Int J Radiat Biol
Pays: England
ID NLM: 8809243

Informations de publication

Date de publication:
03 Oct 2024
Historique:
medline: 4 10 2024
pubmed: 4 10 2024
entrez: 3 10 2024
Statut: aheadofprint

Résumé

Glioblastomas are resistant to conventional therapies, including radiotherapy. Our previous study proved that epigenetic regulation influences the radiation response of glioma cells. This study evaluated the role of the acetyltransferase Tip60 on the radiation response. Tip60 expression was down-regulated by transfecting specific siRNA's in A7 and MO59K cells with high and low expression of Tip60, respectively, and its effect on survival was assessed. DNA repair was analyzed by foci scoring (γH2AX, Rad51, 53BP1, pATM). The interaction of Tip60 with ATM and DNA-PK was investigated using the specific inhibitors KU55933 and NU7441, respectively. Knockdown of Tip60 significantly ( Downregulation of Tip60 enhances the radiation sensitivity of both glioma cells and markedly elevates the radiation sensitivity when combined with DNA-PKi. Therefore, treatment with DNA-PK inhibitors represents a promising approach to augment the radiation sensitivity of glioma cell lines with deficient Tip60 activity in a synergistic manner.

Identifiants

pubmed: 39361872
doi: 10.1080/09553002.2024.2409668
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-11

Auteurs

K Bannik (K)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

A Sak (A)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

M Groneberg (M)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

M Stuschke (M)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

Classifications MeSH