Establishment of acquired radioresistant cells to fractionated radiation from hTERT-immortalized normal human epithelial cell

Senescence-like growth arrest (SLGA), which is a radiation-induced cell death pathway, is induced in immortalized normal human epithelial cell (hTERT-RPE1) by the daily fractionated X-irradiation with 1.5 Gy within 30 times. We here demonstrate that pre-treatment induces acquired radioresistance (ARR) that can survive from the lethal fractionated radiation. The parent cells were daily fractionated with 1.5 Gy for 5 d and then incubated for 7 d without fractionated radiation. After this, the daily fractionated radiation with 1.5 Gy was restarted. A small population of surviving cells appeared after 30 times of the daily fractionated radiation was completed and they were continuously growing up to 120 times of the daily fractionated radiation (RPE1-1.5Fr). We confirmed a higher basal expression level of p53, which functions in the activation of the SLGA pathway but fails to further accumulate after 1.5 Gy of single irradiation in RPE1-1.5Fr. It is the first report to induce ARR phenotype for fractionated radiation in normal human cells.

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Journal
Radiation Protection Dosimetry
Published
2024-11-01
DOI
https://doi.org/10.1093/rpd/ncae118
Primary Topic
DNA Repair Mechanisms
Type
article
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article

Establishment of acquired radioresistant cells to fractionated radiation from hTERT-immortalized normal human epithelial cell

Yohei Inaba, Koichi Chida, Ryuta Ishikawa, Rio Isobe et al.
Radiation Protection Dosimetry
DNA Repair Mechanisms
article

Establishment of acquired radioresistant cells to fractionated radiation from hTERT-immortalized normal human epithelial cell

Yohei Inaba, Koichi Chida, Ryuta Ishikawa, Rio Isobe, Tomisato Miura, Yasushi Kino, Taku Sato, Manabu Fukumoto, Keiji Suzuki, Masatoshi Suzuki
article en

Abstract

Senescence-like growth arrest (SLGA), which is a radiation-induced cell death pathway, is induced in immortalized normal human epithelial cell (hTERT-RPE1) by the daily fractionated X-irradiation with 1.5 Gy within 30 times. We here demonstrate that pre-treatment induces acquired radioresistance (ARR) that can survive from the lethal fractionated radiation. The parent cells were daily fractionated with 1.5 Gy for 5 d and then incubated for 7 d without fractionated radiation. After this, the daily fractionated radiation with 1.5 Gy was restarted. A small population of surviving cells appeared after 30 times of the daily fractionated radiation was completed and they were continuously growing up to 120 times of the daily fractionated radiation (RPE1-1.5Fr). We confirmed a higher basal expression level of p53, which functions in the activation of the SLGA pathway but fails to further accumulate after 1.5 Gy of single irradiation in RPE1-1.5Fr. It is the first report to induce ARR phenotype for fractionated radiation in normal human cells.

Radiation Protection DosimetryVol. 200(16-18)
Hirosaki University (JP), Tohoku University (JP), RIKEN Center for Advanced Intelligence Project (JP), Nagasaki University (JP)
Good health and well-being
Openalex Percentile: Top 82%
DNA Repair Mechanisms
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Establishment of acquired radioresistant cells to fractionated radiation from hTERT-immortalized normal human epithelial cell — Yohei Inaba, Koichi Chida, et al. · Radiation Protection Dosimetry (2024) | TGRS Research Map | TGRS