Effect of uncoupling protein 2 gene on radiation sensitivity of Siha cells

C. Liu, X. Dong, Yuanhang Li, Xinqiang Zhang, Zhicheng Wang, Gang Zhao
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Abstract

Objective To investigate whether silencing UCP2 can sensitize cervical cancer cell line Siha to radiation. Methods Siha cells were transfected with UCP2 siRNA and then irradiated by X-ray. The radiosensitivity of Siha cells was verified by colony formation, CCK-8, apoptosis and immunofluorescence assays. The mitochondrial membrane potential and the production of reactive oxygen species (ROS) were detected to further explore the related mechanism. Results RT-PCR and Western blot assays showed that the expression of UCP2 in Siha cells was increased after irradiation and the UCP2 siRNA successfully silenced the expression of UCP in cells. According to the survival curves, the D0, Dq, N and SF2 were 1.54, 1.31, 2.31 Gy and 0.52 for siUCP2 group, 2.50, 3.64, 4.30 Gy and 0.83 for blank control group, and 3.34, 2.16, 1.91 Gy and 0.69, for siNC group, respectively. The radiosensitivity enhancement ratio of silent group was 0.62 and 0.46, compared with blank control group and negative control group, respectively. The proliferative activity of cells in the silent group was lower than that in the control group (t=13.2, P<0.05). Apoptosis levels in the silent group were significantly higher than those in the control group after irradiation(t=3.14, P<0.05). At 4 h after irradiation, the ROS production in the silent group was significantly higher than that in the control group (t=19.10, P<0.05). At 24 h after irradiation, the mitochondrial membrane potential of Siha cells in the silent group was significantly lower than that in the control group (t=4.18, P<0.05). Conclusions The radiosensitivity of Siha cells is enhanced after UCP2 silencing, and thus UCP2 may applicable as a new target for radiosensitization of cervical cancer cells. Key words: Cervical cancer; RNA interference; Uncoupling protein 2; Apoptosis; Radiation sensitivity
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解偶联蛋白2基因对Siha细胞辐射敏感性的影响
目的探讨沉默UCP2是否能提高宫颈癌Siha细胞对辐射的敏感性。方法用UCP2 siRNA转染Siha细胞,x射线照射。通过菌落形成、CCK-8、细胞凋亡和免疫荧光实验验证Siha细胞的放射敏感性。检测线粒体膜电位和活性氧(ROS)的产生,进一步探讨其相关机制。结果RT-PCR和Western blot检测显示,照射后Siha细胞中UCP2的表达增加,UCP2 siRNA成功地沉默了细胞中UCP的表达。根据生存曲线,siUCP2组的D0、Dq、N和SF2分别为1.54、1.31、2.31 Gy和0.52,空白对照组的D0、Dq、N和SF2分别为2.50、3.64、4.30 Gy和0.83,siNC组的生存曲线分别为3.34、2.16、1.91 Gy和0.69。与空白对照组和阴性对照组相比,沉默组放射敏感性增强比分别为0.62和0.46。沉默组细胞的增殖活性低于对照组(t=13.2, P<0.05)。照射后沉默组细胞凋亡水平显著高于对照组(t=3.14, P<0.05)。照射后4 h,沉默组ROS产量显著高于对照组(t=19.10, P<0.05)。照射后24 h,沉默组Siha细胞线粒体膜电位显著低于对照组(t=4.18, P<0.05)。结论UCP2沉默后Siha细胞的放射敏感性增强,UCP2可作为宫颈癌细胞放射增敏的新靶点。关键词:宫颈癌;RNA干扰;解偶联蛋白2;细胞凋亡;辐射敏感性
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来源期刊
中华放射医学与防护杂志
中华放射医学与防护杂志 Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.60
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0.00%
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6377
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