cGAS Regulates the Radioresistance of Human Head and Neck Squamous Cell Carcinoma Cells

Cyclic GMP-AMP synthase (cGAS) plays an important role in biological responses to pathogens. The activation of the cGAS pathway in immune cells is known to induce antitumor effects, but the role of cGAS in cancer cells remains poorly understood. In silico analysis using public databases suggested that high cGAS expression in head and neck squamous cell carcinoma (HNSCC) is indicative of a poor prognosis for HNSCC patients. We therefore investigated the role of cGAS in malignancies and the cellular radiation response of human HNSCC cells (SAS and Ca9-22) in vitro, because radiotherapy is one of the treatments most commonly used for HNSCC. Although cGAS knockdown failed to suppress the proliferation of non-irradiated HNSCC cells, it enhanced the radiosensitivity of HNSCC cells. The administration of the cGAS agonist increased the radioresistance of HNSCC cells. cGAS knockdown increased radiation-induced mitotic catastrophe, apoptosis, or cellular senescence, depending on the cell line, and this cell line-dependent response might be due to different responses of p21 after irradiation. Collectively, our findings indicate that the cGAS pathway regulates the radioresistance of HNSCC cells.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:11

Enthalten in:

Cells - 11(2022), 9 vom: 23. Apr.

Sprache:

Englisch

Beteiligte Personen:

Nyui, Taichi [VerfasserIn]
Yoshino, Hironori [VerfasserIn]
Nunota, Tetsuya [VerfasserIn]
Sato, Yoshiaki [VerfasserIn]
Tsuruga, Eichi [VerfasserIn]

Links:

Volltext

Themen:

Apoptosis
Cellular senescence
Cyclic GMP-AMP synthase
EC 2.7.7.-
Head and neck squamous cell carcinoma
Journal Article
Mitotic catastrophe
Nucleotidyltransferases
P21
Radiosensitivity
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 18.05.2022

Date Revised 06.02.2023

published: Electronic

Citation Status MEDLINE

doi:

10.3390/cells11091434

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM340866772