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[肿瘤蛋白翻译控制反义RNA1通过靶向miR-30c-5p对肝癌细胞放射敏感性、增殖、迁移和侵袭的影响]

[Effects of tumor protein translation control antisense RNA1 on radiosensitivity, proliferation, migration and invasion of hepatocellular carcinoma cells by targeting miR-30c-5p].

作者信息

Zhai J J, Du X R, Li C X

机构信息

Department of Emergency, Shanxi People's Hospital, Taiyuan 030000, China.

Department of Oncology, Shanxi People's Hospital, Taiyuan 030000, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2021 Oct 23;43(10):1054-1061. doi: 10.3760/cma.j.cn112152-20190709-00426.

Abstract

To investigate the effects of tumor protein translation control antisense RNA1 (TPT1-AS1) on the radiosensitivity, cell proliferation, migration and invasion of hepatocellular carcinoma cells by targeting microRNA-30c-5p (miR-30c-5p). Thirty-four cases of liver cancer tissues and adjacent normal tissues were derived from liver cancer patients who were admitted to Shanxi Provincial People's Hospital from March 2016 to March 2018. Liver cancer HepG2 cell was transfected with negative control siRNA (si-NC group), si-TPT1-AS1 (si-TPT1-AS1 group), pcDNA3.1 (pcDNA3.1 group), pcDNA3.1-TPT1-AS1 (pcDNA3.1-TPT1-AS1 group), si-TPT1-AS1 and anti-miR-NC (si-TPT1-AS1+ anti-miR-NC group), si-TPT1-AS1 and anti-miR-30c-5p (si-TPT1-AS1+ anti-miR-30c-5p group), respectively. Real-time quantitative reverse transcription polymerase chain reaction (qPCR) was used to detect the transcription levels of TPT1-AS1 and miR-30c-5p in normal tissues adjacent to cancer and liver cancer tissues, the clone formation test was used to test the radiosensitivity of HepG2 cells, and the Methyl Thiazolyl Tetrazolium (MTT) test was used to test the proliferation of HepG2 cells. Cell cycle distribution was detected by flow cytometry, Transwell array was used to detect the migration and invasion ability of HepG2 cells, dual luciferase reporter array was used to verify the targeting relationship of TPT1-AS1 and miR-30c-5p, western blot was used to detect the expressions of proliferation, migration and invasion-related proteins. The expression levels of TPT1-AS1 and miR-30c-5p in liver cancer tissues were 0.84±0.08 and 0.13±0.01, statistically different from 0.31±0.03 and 0.50±0.05 in normal tissues adjacent to cancer (<0.05). When the cells were treated with 2, 4, 6, 8 Gy irradiation, the cell survival scores of the si-TPT1-AS1 group were 0.280±0.040, 0.069±0.011, 0.020±0.003 and 0.005±0.001, respectively, lower than 0.648±0.070, 0.348±0.080, 0.130±0.020 and 0.060±0.009 of the si-NC group (<0.05), the radiosensitization ratio of the si-TPT1-AS1 group was 1.672. The number of cell migration and invasion in the si-TPT1-AS1 group were (50.00±4.36) and (44.00±4.03), respectively, which were lower than (109.00±8.68) and (94.00±7.49) in the si-NC group (<0.05), the cell absorbance () values at 24, 48 and 72 hours were 0.28±0.03, 0.43±0.04 and 0.68±0.07, respectively, lower than 0.46±0.04, 0.87±0.08 and 1.35±0.13 of the si-NC group (<0.05), the protein expression levels of Cyclin D1, p21, E-cadherin and MMP-2 were 0.25±0.02, 0.65±0.06, 0.68±0.07 and 0.27±0.03, respectively, statistically different from 0.88±0.08, 0.17±0.02, 0.14±0.01 and 0.89±0.09 of si-NC group (<0.05), the proportions of S phase and G(2) phase in the si-TPT1-AS1 group were (17.82±1.03)% and (34.15±2.29)%, respectively, significantly different from (35.14±2.61)% and (16.84±1.21)% in the si-NC group (<0.05). The luciferase activity of cells in the WT-TPT1-AS1+ miR-30c-5p group was 0.26±0.02, lower than 0.92±0.09 in the WT-TPT1-AS1+ miR-NC group (<0.05). The cell survival scores in the si-TPT1-AS1+ anti-miR-30c-5p group were 0.450±0.081, 0.200+ 0.045, 0.070±0.010, 0.026±0.004 after treatment with 2, 4, 6, 8 Gy irradiation, higher than 0.285±0.043, 0.075±0.014, 0.028±0.004, 0.006±0.001 of si-TPT1-AS1+ anti-miR-NC group (<0.05). The radiosensitization ratio of the si-TPT1-AS1+ anti-miR-30c-5p group was 0.694. The number of migration and invasion in the si-TPT1-AS1+ anti-miR-30c-5p group were 79.00±6.65 and 68.00±6.33, higher than (52.00±4.41) and (46.00±4.06) of si-TPT1-AS1+ anti-miR-NC Group (<0.05), the values at 24, 48 and 72 hours were 0.37±0.03, 0.64±0.06 and 0.96±0.09, respectively, higher than 0.26±0.03, 0.41±0.04, and 0.65±0.06 of si-TPT1-AS1+ anti-miR-NC group (<0.05), the expression levels of Cyclin D1, p21, E-cadherin and MMP-2 protein were 0.57±0.06, 0.43±0.04, 0.43±0.04 and 0.64±0.06, statistically different from 0.24±0.02, 0.66±0.06, 0.65±0.06 and 0.28±0.03 of the si-TPT1-AS1+ anti-miR-NC group (<0.05). The expression of TPT1-AS1 up-regulates in the liver cancer tissues. TPT1-AS1 may down-regulate miR-30c-5p expression, reduce the radiosensitivity of liver cancer cells, and promote the proliferation, migration and invasion of liver cancer cells.

摘要

通过靶向微小RNA-30c-5p(miR-30c-5p)研究肿瘤蛋白翻译控制反义RNA1(TPT1-AS1)对肝癌细胞放射敏感性、细胞增殖、迁移和侵袭的影响。收集2016年3月至2018年3月在山西省人民医院住院的肝癌患者的34例肝癌组织及癌旁正常组织。将肝癌HepG2细胞分别转染阴性对照小干扰RNA(si-NC组)、si-TPT1-AS1(si-TPT1-AS1组)、pcDNA3.1(pcDNA3.1组)、pcDNA3.1-TPT1-AS1(pcDNA3.1-TPT1-AS1组)、si-TPT1-AS1与抗miR-NC(si-TPT1-AS1+抗miR-NC组)、si-TPT1-AS1与抗miR-30c-5p(si-TPT1-AS1+抗miR-30c-5p组)。采用实时定量逆转录聚合酶链反应(qPCR)检测癌旁正常组织和肝癌组织中TPT1-AS1和miR-30c-5p的转录水平,克隆形成试验检测HepG2细胞的放射敏感性,甲基噻唑基四氮唑(MTT)试验检测HepG2细胞的增殖情况。通过流式细胞术检测细胞周期分布,Transwell小室检测HepG2细胞的迁移和侵袭能力,双荧光素酶报告基因检测验证TPT1-AS1与miR-30c-5p的靶向关系,蛋白质免疫印迹法检测增殖、迁移和侵袭相关蛋白的表达。肝癌组织中TPT1-AS1和miR-30c-5p的表达水平分别为0.84±0.08和0.13±0.01,与癌旁正常组织中的0.31±0.03和0.50±0.05相比,差异有统计学意义(<0.05)。当细胞接受2、4、6、8 Gy照射时,si-TPT1-AS1组的细胞存活分数分别为0.280±0.040、0.069±0.011、0.020±0.003和0.005±0.001,低于si-NC组的0.648±0.070、0.348±0.080、0.130±0.020和0.060±0.009(<0.05),si-TPT1-AS1组的放射增敏比为1.672。si-TPT1-AS1组的细胞迁移和侵袭数分别为(50.00±4.36)和(44.00±4.03),低于si-NC组的(109.00±8.68)和(94.00±7.49)(<0.05),24、48和72小时的细胞吸光度()值分别为- 0.28±0.03、0.43±0.04和0.68±0.07,低于si-NC组的0.46±0.04、0.87±0.08和1.35±0.13(<0.05),细胞周期蛋白D1、p21、E-钙黏蛋白和基质金属蛋白酶-2的蛋白表达水平分别为0.25±0.02、0.65±0.06、0.68±0.07和0.27±0.03,与si-NC组的0.88±0.08、0.17±0.02、0.14±0.01和0.89±0.09相比,差异有统计学意义(<0.05),si-TPT1-AS1组S期和G(2)期的比例分别为(17.82±1.03)%和(34.15±2.29)%,与si-NC组的(35.14±2.61)%和(16.84±1.21)%相比,差异有统计学意义(<0.05)。WT-TPT1-AS1+miR-30c-5p组细胞的荧光素酶活性为0.26±0.02,低于WT-TPT1-AS1+miR-NC组的0.92±0.09(<0.05)。si-TPT1-AS1+抗miR-30c-5p组在接受2、4、6、8 Gy照射后的细胞存活分数分别为0.450±0.081、0.200+0.045、0.070±0.010、0.026±0.004,高于si-TPT1-AS1+抗miR-NC组的0.285±0.043、0.075±0.014、0.028±0.004、0.006±0.001(<0.05)。si-TPT1-AS1+抗miR-30c-5p组的放射增敏比为0.694。si-TPT1-AS1+抗miR-30c-5p组的迁移和侵袭数分别为79.00±6.65和68.00±6.33,高于si-TPT1-AS1+抗miR-NC组的(52.00±4.41)和(46.00±4.06)(<0.05),24、48和72小时的 值分别为0.37±0.03、0.64±0.06和0.96±0.09,高于si-TPT1-AS1+抗miR-NC组的0.26±0.03、0.41±0.04和0.65±0.06(<0.05),细胞周期蛋白D1、p21、E-钙黏蛋白和基质金属蛋白酶-·2蛋白的表达水平分别为0.57±0.06、0.43±0.04、0.43±0.04和0.64±0.06,与si-TPT1-AS1+抗miR-NC组的0.24±0.02、0.66±0.06、0.65±0.06和0.28±0.03相比,差异有统计学意义(<0.05)。肝癌组织中TPT1-AS1表达上调。TPT1-AS1可能下调miR-30c-5p表达,降低肝癌细胞的放射敏感性,并促进肝癌细胞的增殖、迁移和侵袭。

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