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首页|期刊导航|中国耳鼻咽喉头颈外科|反义细胞角蛋白13基因对人鼻咽癌HNE1细胞移植瘤放疗敏感性的影响

反义细胞角蛋白13基因对人鼻咽癌HNE1细胞移植瘤放疗敏感性的影响

苗春雨 余宏

中国耳鼻咽喉头颈外科2016,Vol.23Issue(5):253-258,6.
中国耳鼻咽喉头颈外科2016,Vol.23Issue(5):253-258,6.DOI:10.16066/j.1672-7002.2016.05.003

反义细胞角蛋白13基因对人鼻咽癌HNE1细胞移植瘤放疗敏感性的影响

Effect of antisense CK13 genes on human nasopharyngeal carcinoma HNE1 cell transplantation tumor

苗春雨 1余宏1

作者信息

  • 1. 昆明医科大学第四附属医院耳鼻咽喉科,云南 昆明650000
  • 折叠

摘要

Abstract

[ABSTRACT]OBJECTIVEThe influnence of observation on the antisense cytokeratin 13 (CK13) gene in nasopharyngeal carcinoma HNE1 cell transplantation tumor radiation sensitivity.METHODSHNE1 cell lines can be divided into control group: the control group (HNE1 cell) and lentivirus (transfection slow virus empty carrier) group and experimental group: HNE1-anti-CK13a (transfection antisense CK13a slow virus) and HNE1-anti-CK13b (transfection antisense slow virus CK13b) four groups, set up a corresponding animal model, after radiotherapy by flow cytometry, immunohistochemistry, PCR, Tunel method and Westernblotting detection.RESULTSThe cell cyclede tection of plasmid transfection slow virus group compared with control group after radiotherapy G2/M phase of the block were significantly prolonged; Immunohistochemical results showed emigration tumor CK13 expression decreased in the experimental group; Tunel method to detect apoptosis necrosis rate found that the experimental group,apoptosis rate significantly decreased; Western blotting detection caspase3 apoptosis markers. PCR to detect CDC25mRNA level decreased obviously.CONCLUSIONAntisense CK13 gene by regulating the cell cycle and apoptosis can reduce HNE1 transplantation tumor radiotherapy of nasopharyngeal carcinoma (NPC) sensitivity, and with the caspase 3 apoptotic pathways and CDC25 signaling pathways.

关键词

鼻咽肿瘤/细胞凋亡/细胞周期/反义细胞角蛋白13

Key words

Nasopharyngeal Neoplasms/Apoptosis/Cell Cycle/anti-cytokeratin 13

引用本文复制引用

苗春雨,余宏..反义细胞角蛋白13基因对人鼻咽癌HNE1细胞移植瘤放疗敏感性的影响[J].中国耳鼻咽喉头颈外科,2016,23(5):253-258,6.

基金项目

云南省科技厅昆明医科大联合专项资金资助 ()

中国耳鼻咽喉头颈外科

OACSCDCSTPCD

1672-7002

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