Back to Search Start Over

Mechanism of the Radioresistant Colorectal Cancer Cell Line SW480RR Established after Fractionated X Irradiation.

Authors :
Yamashita, Koya
Yasui, Hironobu
Bo, Tomoki
Fujimoto, Masaki
Inanami, Osamu
Source :
Radiation Research; 2024, Vol. 201 Issue 7, p38-50, 13p
Publication Year :
2024

Abstract

Radioresistant cancer cells are risk factors for recurrence and are occasionally detected in recurrent tumors after radiotherapy. Intratumor heterogeneity is believed to be a potential cause of treatment resistance. Heterogeneity in DNA content has also been reported in human colorectal cancer; however, little is known about how such heterogeneity changes with radiotherapy or how it affects cancer radioresistance. In the present study, we established radioresistant clone SW480RR cells after fractionated X-ray irradiation of human colorectal cancer-derived SW480.hu cells, which are composed of two cell populations with different chromosome numbers, and examined how cellular radioresistance changed with fractionated radiotherapy. Compared with the parental cell population, which mostly comprised cells with higher ploidy, the radioresistant clones showed lower ploidy and less initial DNA damage. The lower ploidy cells in the parental cell population were identified as having radioresistance prior to irradiation; thus, SW480RR cells were considered intrinsically radioresistant cells selected from the parental population through fractionated irradiation. This study presents a practical example of the emergence of radioresistant cells from a cell population with ploidy heterogeneity after irradiation. The most likely mechanism is the selection of an intrinsically radioresistant population after fractionated X-ray irradiation, with a background in which lower ploidy cells exhibit lower initial DNA damage. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00337587
Volume :
201
Issue :
7
Database :
Complementary Index
Journal :
Radiation Research
Publication Type :
Academic Journal
Accession number :
178212144
Full Text :
https://doi.org/10.1667/RADE-23-00021.1