Shi Fenglian,Wei Ying,Liu Junling.The role of miRNA-95 in radiosensitivity of cervical cancer cells[J].Chinese Journal of Radiological Medicine and Protection,2018,38(11):807-814
The role of miRNA-95 in radiosensitivity of cervical cancer cells
Received:April 11, 2018  
DOI:10.3760/cma.j.issn.0254-5098.2018.11.002
KeyWords:miRNA-95  Cervical cancer  Radiotherapy sensitivity  Cell proliferation  Apoptosis
FundProject:河南省医学科技攻关支持项目基金(2014000157)
Author NameAffiliationE-mail
Shi Fenglian Department of Gynecology and Obstetrics, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, China shifengliansci@163.com 
Wei Ying Department of Gynecology and Obstetrics, Huashan Central Hospital, Xi'an 710043, China  
Liu Junling Department of Pathology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, China  
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Abstract::
      Objective To detect the expression of miRNA-95 in cervical cancer tissues and cell lines with different radiosensitivity and study the effect of its regulation on radiosensitivity of cervical cancer cells. Methods Real-time PCR was used to detect the expression of miRNA-95 in cervical cancer tissues of 20 patients with radiosensitivity, 20 patients with radiation tolerance, radioresistant cervical cancer cell lines (HeLa, SiHa), and radiosensitive cervical cancer cell lines (Me180). MiRNA-95 mimics (miRNA-95 mimics group)and miRNA-95 inhibition (miRNA-95 inhibition group)were transfected into radioresistant HeLa and SiHa cells by liposome 2000, miRNA-NC was set as control group. CCk-8 assay was used to detect the proliferation of cervical cancer cells irradiated with 60Co γ-rays at 0,2,4,6,8,10 Gy. After 4 Gy irradiation, cell clonal formation ability was detected by plate monoclonal assay, and cell apoptosis was detected by flow cytometry. Dual luciferase activity assay was used to detect the target gene of miRNA-95 in cervical cancer cells. Nude mice were used to detect the changes of tumor formation ability. Results The expression of miRNA-95 in cervical cancer tissues of patients with radiotherapy tolerance was significantly higher than that of patients with radiotherapy sensitivity (t=12.279, P<0.05). The expressions of miRNA-95 in HeLa and SiHa cells were significantly higher those that of Me180 cells (t=5.162, 7.114, P<0.05). When the cells were treated with miRNA-95 inhibition, the expression of miRNA-95 in HeLa and SiHa cell lines was significantly lower than that of microRNA-NC group (t=5.162, 7.114, P<0.05), the cell proliferation rate decreased significantly (t=8.273, 11.354, 13.489, 15.396 and 6.197, 9.185, 10.994, 12.442, P<0.05), the cell monoclonal formation rate decreased significantly (t=8.378, 7.931, P<0.05), and the apoptosis rate increased significantly (t=10.265, 8.386, P<0.05). The tumorigenic weight of nude mice in the miRNA95 inhibition group was significantly decreased (t=8.881, 10.037, P<0.05). Conclusions The miRNA-95 had low levels in both radiosensitive cervical cancer tissues and cells. Inhibiting the expression of microRNA-95 can significantly improve the radiosensitivity of cervical cancer cells by targeting SGPP1 gene.
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