|Table of Contents|

The effect and mechanism of Serglycin stable interference on the sensitivity of nasopharyngeal carcinoma cells with high metastatic cells to cisplatin

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2017 06
Page:
856-859
Research Field:
Publishing date:

Info

Title:
The effect and mechanism of Serglycin stable interference on the sensitivity of nasopharyngeal carcinoma cells with high metastatic cells to cisplatin
Author(s):
Liang Wanning1Wu Wenqiang2Chen Wenhua3Lan Zhong4
1.Pharmaceutical Department;2.Oncology Department,Zhaoqing People's Hospital,Guangdong Zhaoqing 526040,China;3.Pharmaceutical Department,Southern Medical University,Guangdong Guangzhou 510515,China;4.Clinical Pharmaceutics Department,Maoming People's Hospital,Guangdong Maoming 525000,China.
Keywords:
Serglycinstable interferencenasopharyngeal carcinomacisplatin sensitivity
PACS:
R739.6
DOI:
10.3969/j.issn.1672-4992.2017.06.005
Abstract:
Objective:To observe the effect of Serglycin on the stability of high metastatic cells of nasopharyngeal carcinoma with high sensitivity to cisplatin,and to explore the mechanism of interference.Methods:Serglycin stable interference of nasopharyngeal carcinoma with high metastatic cell lines were divided into three groups:experimental group 5-8f KDA and 5-8f KDC and control group 5-8f scrambled.To detect Serglycin protein expression,to observe the parental and stable plant cell morphology.MTT assay was used to detect the absorbance,draw the curve of the proliferation under the effect of cisplatin.To detect cell viability,stem cell gene expression,and content of Vimentin and E-cadherin.Results:In the experimental group,the expression of Serglycin gene was inhibited.The Serglycin gene expression in the control group was more.The difference was significant,with statistical significance(P<0.05).The secreted Serglycin protein in the experimental group was significantly decreased,and the expression of Serglycin in the control group was higher.The cell morphology of the stable group was round or polygon,and the control group cells were spindle shaped.MTT was found to be significantly faster in the control group than in the third day after cisplatin,and there was statistical significance(P<0.05).Compared with the 5-8f scrambled group,the cell survival rate of the experimental group was significantly decreased,and the cell survival rate was statistically significant(P<0.05).In stable group,the expression of gene expression was significantly decreased,and the difference was significant(P<0.05).Serglycin can promote the expression of Vimentin protein and inhibit the expression of E-cadherin protein in tumor tissue.Conclusion:Serglycin can increase the sensitivity of nasopharyngeal carcinoma cells with high metastatic cells to cisplatin.

References:

[1]Chu Qiaoqiao,Liu Tao,Jia Shouwei,et al.Serglycin stable interference with increased sensitivity to cisplatin in nasopharyngeal carcinoma with high metastatic cells [J].Chin J Pharmaceutical Sciences,2015,50(8):676-680.[储悄悄,刘韬,贾守薇,等.Serglycin稳定干扰增加鼻咽癌高转移细胞对顺铂的敏感性[J].中国药学杂志,2015,50(8):676-680.]
[2]Kwok H,Wu CW,Palser AL,et al.Genomic diversity of Epstein-Barr virus genomes isolated from primary nasopharyngeal carcinoma biopsy samples[J].J Virology,2014,88(18):10662-10672.
[3]Xu Zhiyuan.Study on the radiation sensitivity of human nasopharyngeal carcinoma cell line [D].Shantou:Shantou University,2007.[徐志渊.人鼻咽癌耐顺铂细胞系的放射敏感性研究[D].汕头:汕头大学,2007.]
[4]Gong Z,Qian Y,Zeng Z,et al.An integrative transcriptomic analysis reveals p53 regulated miRNA,mRNA,and lncRNA networks in nasopharyngeal carcinoma[J].Tumor Biology,2015,37(3):1-13.
[5]Jiang H,Gao M,Shen Z,et al.Blocking PI3K/Akt signaling attenuates metastasis of nasopharyngeal carcinoma cells through induction of mesenchymal-epithelial reverting transition[J].Oncology Reports,2014,32(2):559-566.
[6]Yi HM,Yi H,Zhu JF,et al.A five-variable signature predicts radioresistance and prognosis in nasopharyngeal carcinoma patients receiving radical radiotherapy[J].Tumor Biology,2015,37(3):1-9.
[7]Lee AW,Law SC,Ng SH,et al.Retrospective analysis of nasopharyngeal carcinoma treated during 1976-1985:Late complications following megavoltage irradiation[J].British J Radiology,2014,65(778):918-928.
[8]Chua MK,Wee JTS,Hui EP,et al.Nasopharyngeal carcinoma[J].Lancet,2015,7(3):388-393.
[9]Wu Fang.Multi center,open,randomized controlled study of advanced nasopharyngeal carcinoma treated with radiotherapy and chemotherapy[D].Nanning:Guangxi Medical University,2014.[吴芳.放化综合治疗局部晚期鼻咽癌的多中心、开放性、随机对照研究[D].南宁:广西医科大学,2014.]
[10]Li Dan.Experimental study on the effect of continuous chemotherapy with small dose of cisplatin on CNE-1 cell kinetics and radiation sensitivity of nasopharyngeal carcinoma [D].Suzhou:Soochow University,2009.[李丹.小剂量顺铂连续化疗对鼻咽癌CNE-1细胞动力学以及放射敏感性影响的实验研究[D].苏州:苏州大学,2009.]
[11]Li XJ,Ong CK,Cao Y,et al.Serglycin is a theranostic target in nasopharyngeal carcinoma that promotes metastasis[J].Cancer Res,2011,71(8):3162-3172.
[12]Tsao SW,Yip YL,Chi MT,et al.Etiological factors of nasopharyngeal carcinoma[J].Oral Oncology,2014,50(5):330-338.
[13]Kolset SO,Pejler G.Serglycin:A structural and functional chame-leon with wide impact on immune cells[J].J Immunol,2011,187(10):4927-4933.

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Last Update: 2017-01-26