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DNA damage response following X-irradiation in oral cancer cell lines HSC3 and HSC4.

Authors :
Jiaranuchart, Sirimanas
Kaida, Atsushi
Onozato, Yusuke
Harada, Hiroyuki
Miura, Masahiko
Source :
Archives of Oral Biology. Jun2018, Vol. 90, p1-8. 8p.
Publication Year :
2018

Abstract

Objective The objective of this study was to characterize the DNA damage response in two human oral cancer cell lines following X-irradiation. Design To visualize radiation-induced cell cycle alterations, two human oral cancer cell lines, HSC3 and HSC4, expressing fluorescent ubiquitination-based cell cycle indicator (Fucci) were established in this study. G2 arrest kinetics following irradiation were obtained from two-color flow cytometric analysis and pedigrees of Fucci fluorescence. DNA double strand break repair kinetics were obtained from immunofluorescence staining for phosphorylated histone H2AX, p53-binding protein 1, phosphorylated DNA-dependent protein kinase catalytic subunit, and breast cancer susceptibility gene 1. Results Both cell lines showed apparent G2 arrest after 10 Gy of irradiation, but it was more enhanced in the HSC3-Fucci cells. Radiosensitivity was higher in the HSC3-Fucci cells than in HSC4-Fucci cells. Pedigree analysis of Fucci fluorescence revealed that the HSC3-Fucci cells exhibited a significantly longer green phase (normally indicating S/G2/M phases, but here reflective of G2 arrest) when irradiated in the red phase (G1 phase) than HSC4-Fucci cells irradiated in either red or green phases. Non-homologous end joining was marginally suppressed during the G1 phase and markedly more likely to be impaired during the S/G2 phases in HSC3-Fucci cells. When G2 arrest was abrogated by checkpoint kinase 1 or Wee1 inhibitors, only HSC4-Fucci cells exhibited radiosensitization. Conclusions We characterized DNA damage response in HSC3-Fucci and HSC4-Fucci cells following irradiation and the former demonstrated inefficient non-homologous end joining, especially during the S/G2 phases, resulting in enhanced G2 arrest. These findings may have clinical implications for oral cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00039969
Volume :
90
Database :
Academic Search Index
Journal :
Archives of Oral Biology
Publication Type :
Academic Journal
Accession number :
128983898
Full Text :
https://doi.org/10.1016/j.archoralbio.2018.02.016