{"title":"Establishment and biological characterization of radioresistant colorectal cancer cell lines.","authors":"Tian-Yin Qu, Qing Dai, Jing Leng, Lin Fang, Jing-Jing Ma, Rui Chen, Che Chen, Peng-Fei Ran, Wen-Wen Zhou, Chang Liu, Huang-Fei Yu","doi":"10.1002/2211-5463.70016","DOIUrl":null,"url":null,"abstract":"<p><p>Radiotherapy resistance is a major cause of recurrence and metastasis in colorectal cancer (CRC). We established radiotherapy-resistant cell lines to explore the molecular mechanisms of radiotherapy resistance in CRC. HT29 and HCT116 cells were subjected to repeated irradiation at 2 Gy to establish these lines. CCK-8 assay, colony formation, and xenograft tumor experiments were used to detect the radiosensitivity of the cells. DNA damage repair proteins, GSH content, and intracellular ROS were also assayed in parental and resistant cells. We successfully established HT29R and HCT116R radioresistant cell lines after fractionated irradiation, and the cells showed significant tolerance to further irradiation compared with the parental cells and a stronger capacity for DNA damage repair. Meanwhile, ionizing radiation significantly reduced GSH in HT29 and HCT116 parental cells but had no effect on GSH content in resistant cells. These results demonstrate that radioresistant colorectal cancer cell lines were successfully established by the method of continuous irradiation with 2 Gy. This provides a basis for further exploration of the mechanism of colorectal cancer radiotherapy resistance.</p>","PeriodicalId":12187,"journal":{"name":"FEBS Open Bio","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEBS Open Bio","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/2211-5463.70016","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Radiotherapy resistance is a major cause of recurrence and metastasis in colorectal cancer (CRC). We established radiotherapy-resistant cell lines to explore the molecular mechanisms of radiotherapy resistance in CRC. HT29 and HCT116 cells were subjected to repeated irradiation at 2 Gy to establish these lines. CCK-8 assay, colony formation, and xenograft tumor experiments were used to detect the radiosensitivity of the cells. DNA damage repair proteins, GSH content, and intracellular ROS were also assayed in parental and resistant cells. We successfully established HT29R and HCT116R radioresistant cell lines after fractionated irradiation, and the cells showed significant tolerance to further irradiation compared with the parental cells and a stronger capacity for DNA damage repair. Meanwhile, ionizing radiation significantly reduced GSH in HT29 and HCT116 parental cells but had no effect on GSH content in resistant cells. These results demonstrate that radioresistant colorectal cancer cell lines were successfully established by the method of continuous irradiation with 2 Gy. This provides a basis for further exploration of the mechanism of colorectal cancer radiotherapy resistance.
期刊介绍:
FEBS Open Bio is an online-only open access journal for the rapid publication of research articles in molecular and cellular life sciences in both health and disease. The journal''s peer review process focuses on the technical soundness of papers, leaving the assessment of their impact and importance to the scientific community.
FEBS Open Bio is owned by the Federation of European Biochemical Societies (FEBS), a not-for-profit organization, and is published on behalf of FEBS by FEBS Press and Wiley. Any income from the journal will be used to support scientists through fellowships, courses, travel grants, prizes and other FEBS initiatives.