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RNA干扰TRAP1表达抑制CD133+CD44+喉癌干细胞生长并促进凋亡

薛海涛 苏静 陈帅 陈春菊 张继华 田君海 董凯峰

中国组织工程研究2017,Vol.21Issue(17):2672-2677,6.
中国组织工程研究2017,Vol.21Issue(17):2672-2677,6.DOI:10.3969/j.issn.2095-4344.2017.17.008

RNA干扰TRAP1表达抑制CD133+CD44+喉癌干细胞生长并促进凋亡

RNA interference targeting inhibition of TRAP1 suppresses cell growth and promotes apoptosis in CD133+CD44+ laryngeal carcinoma stem cells

薛海涛 1苏静 1陈帅 1陈春菊 1张继华 1田君海 1董凯峰1

作者信息

  • 1. 河北医科大学第一医院耳鼻咽喉科,河北省石家庄市 050031
  • 折叠

摘要

Abstract

BACKGROUND: Tumor necrosis factor-associated protein 1 (TRAP1) is a heat-shock protein 90-related mitochondrial chaperone. Accumulative evidence has demonstrated that TRAP1 overexpression is closely related to carcinogenesis. However, the exact function and mechanism of TRAP1 in the occurrence of laryngeal carcinoma remains unclear. OBJECTIVE: To investigate whether RNA interference can inhibit TRAP1 overexpression and to explore its effects on growth and apoptosis of CD133+CD44+ laryngeal carcinoma stem cells. METHODS: CD133+CD44+ laryngeal carcinoma stem cells were sorted from human laryngeal carcinoma Hep-2 cellsusing immunomagnetic beads. The shRNA sequence of TRAP1 was designed and synthesized and CD133+CD44+ laryngeal carcinoma stem cells were transfected with LipofectamineTM 2000. Cell counting kit-8 assay, colony formation assay and flow cytometry were used to investigate the effects of interference of TRAP1 expression on growth and apoptosis of CD133+CD44+ laryngeal carcinoma stem cells. Spectrophotometric method was used to detect the activity of caspase-3, -8 and -9. RESULTS AND CONCLUSION: TRAP1 mRNA and protein expression levels were significantly decreased in TRAP1 shRNA-transfected CD133+CD44+ laryngeal carcinoma stem cells (P < 0.01). Compared with the blank control and negative control groups, the growth and colony formation of CD133+CD44+ laryngeal carcinoma stem cells were significantly inhibited in the TRAP1 shRNA-transfected group (P < 0.05). Apoptosis of CD133+CD44+ laryngeal carcinoma stem cells was significantly inhibited in the TRAP1 shRNA-transfected group as compared with the blank control and negative control groups (P < 0.05). TRAP1 shRNA-mediated cell apoptosis was associated with the activation of caspase-3, -8 and -9. These results suggest that RNA interference targeting inhibition of TRAP1 suppresses cell growth but promotes apoptosis in CD133+CD44+ aryngeal carcinoma stem cells. TRAP1 is likely to be a gene target for treatment of laryngeal carcinoma.

关键词

干细胞/肿瘤干细胞/喉鳞癌/CD44/CD133/TRAP1/RNA干扰/细胞凋亡/细胞增殖

分类

医药卫生

引用本文复制引用

薛海涛,苏静,陈帅,陈春菊,张继华,田君海,董凯峰..RNA干扰TRAP1表达抑制CD133+CD44+喉癌干细胞生长并促进凋亡[J].中国组织工程研究,2017,21(17):2672-2677,6.

基金项目

河北省重点研发计划(152777179),项目名称:TRAP1 在人喉鳞癌中的表达及其与化疗抵抗的关系研究the Key Research and Development Project of Hebei Province, No. 152777179 (152777179)

中国组织工程研究

OA北大核心CSTPCD

2095-4344

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