Ding Ku-Ke, Yang Fen, Jiang Hui-Qing, Yuan Zeng-Qiang, Yin Ling-Ling, Dong Ling-Yue, Cui Wei, Gou Qiao, Liu Xiao-Dan, Wu Yu-Mei, Jiang Xiao-Yan, Zhang Xin, Zhou Ping-Kun, Yang Chuan-Jie
National Institute for Radiological Protection, Chinese Center for Disease Control and Prevention, Beijing 100088, P.R. China.
Key Laboratory of Radiological Protection and Nuclear Emergency, Chinese Center for Disease Control and Prevention, Beijing 100088, P.R. China.
Oncol Lett. 2019 Sep;18(3):2704-2711. doi: 10.3892/ol.2019.10590. Epub 2019 Jul 9.
The effects of the immediate early response 5 () gene on the sensitivity of HeLa cells to radiation remain unclear. In the present study, stably transfected HeLa cells resulting in the knockdown or overexpression of were investigated. In addition, xenografts of normal, -silenced and -overexpressed HeLa cells were injected into nude mice and examined. The results demonstrated that the radiosensitivity of the -overexpressed HeLa cells was significantly increased compared with that of the normal and -silenced cells. The upregulation of effectively decreased cell proliferation and silencing promoted cell proliferation compared with that in the normal HeLa cells. Following irradiation of the cells with knockdown, cell cycle was arrested at the G/M phase and an increase in the proportion of S phase cells was observed. By contrast, the overexpression of 5 led to an increase in the proportion of G phase cells. Furthermore, the upregulation of inhibited tumor growth . The present findings demonstrate that the gene affects the radiosensitivity of HeLa cells and serves an important role in cell proliferation, suggesting that this gene may be a potential radiotherapeutic target in cervical cancer.
立即早期反应5()基因对HeLa细胞辐射敏感性的影响尚不清楚。在本研究中,对导致该基因敲低或过表达的稳定转染HeLa细胞进行了研究。此外,将正常、基因沉默和基因过表达的HeLa细胞异种移植到裸鼠体内并进行检测。结果表明,与正常细胞和基因沉默细胞相比,基因过表达的HeLa细胞的辐射敏感性显著增加。与正常HeLa细胞相比,该基因的上调有效降低了细胞增殖,而基因沉默则促进了细胞增殖。在对基因敲低的细胞进行照射后,细胞周期停滞在G/M期,并且观察到S期细胞比例增加。相比之下,该基因的过表达导致G期细胞比例增加。此外,该基因的上调抑制了肿瘤生长。本研究结果表明,该基因影响HeLa细胞的辐射敏感性,并在细胞增殖中起重要作用,提示该基因可能是宫颈癌潜在的放射治疗靶点。