Establishment and biological characterization of radioresistant colorectal cancer cell lines.

IF 2.8 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
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
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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.

结直肠癌放射耐药细胞系的建立及生物学特性研究。
放疗抵抗是结直肠癌复发和转移的主要原因。我们建立放疗耐药细胞系,探讨结直肠癌放疗耐药的分子机制。HT29和HCT116细胞在2gy的辐照下反复建立这些细胞系。采用CCK-8法、集落形成法和异种移植肿瘤实验检测细胞的放射敏感性。DNA损伤修复蛋白、GSH含量和细胞内ROS也在亲本和抗性细胞中进行了检测。我们成功建立了HT29R和HCT116R分离辐照后的耐辐射细胞系,与亲本细胞相比,细胞对进一步辐照表现出明显的耐受性,并具有更强的DNA损伤修复能力。同时,电离辐射显著降低了HT29和HCT116亲本细胞的GSH含量,但对抗性细胞的GSH含量没有影响。结果表明,采用2 Gy连续照射的方法成功建立了耐辐射的结直肠癌细胞系。这为进一步探讨结直肠癌放疗耐药机制提供了基础。
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来源期刊
FEBS Open Bio
FEBS Open Bio BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
5.10
自引率
0.00%
发文量
173
审稿时长
10 weeks
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.
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