Sun Chaonan,Qiao Qiao,Li Guang,Han Chuyang,Han Ning,Zhang Miao.Endoplasmic reticulum stress inhibitor salubrinal enhanced radiosensitivity of head and neck carcinoma cells[J].Chinese Journal of Radiological Medicine and Protection,2017,37(3):177-181
Endoplasmic reticulum stress inhibitor salubrinal enhanced radiosensitivity of head and neck carcinoma cells
Received:October 17, 2016  
DOI:10.3760/cma.j.issn.0254-5098.2017.03.003
KeyWords:Head and neck squamous carcinoma  Radiosensitivity  Endoplasmic reticulum stress pathway inhibitor  Glucose regulated proteins 78
FundProject:国家自然科学基金(81402521)
Author NameAffiliationE-mail
Sun Chaonan Department of Radiotherapy, the First Hospital of China Medical University, Shenyang 110001, China  
Qiao Qiao Department of Radiotherapy, the First Hospital of China Medical University, Shenyang 110001, China  
Li Guang Department of Radiotherapy, the First Hospital of China Medical University, Shenyang 110001, China 13804058616@163.com 
Han Chuyang Department of Radiotherapy, the First Hospital of China Medical University, Shenyang 110001, China  
Han Ning Department of Radiotherapy, the First Hospital of China Medical University, Shenyang 110001, China  
Zhang Miao Department of Radiotherapy, the First Hospital of China Medical University, Shenyang 110001, China  
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Abstract::
      Objective To explore the effect of salubrinal (sal, an endoplasmic reticulum stress inhibitor) on radiosensitivity of human head and neck squamous carcinoma cells (HNSCC). Methods Cells were divided into two groups of sal treatment and its control. For drug treatment group, cells were treated with 10 mmol/L sal for different time (12, 24, 36 h) and then irradiated. The levels of a core protein GRP78 of endoplasmic reticulum stress (ERS) in HNSCC(KB, Fadu, and Detroit 562 cells)were analyzed by Western blot assay at different time (0, 20 min,1 h, 3 h, 6 h, 12 h, 24 h and 48 h) after irradiation. Cell survival was measured with colony formation assay. Results Western blot assay revealed that the protein levels of GRP78 in three kinds of HNSCC significantly increased from 20 min to 1 h and peaked at 3 h after radiation (t=12.72, 13.37, 18.31, P<0.05). Compared with the control group, treatment of cells with sal decreased GRP78 protein levels (t=14.25, 5.34, 3.12, P<0.05) in three cell lines and also significantly enhanced radiation damage and reduced cell viability. The sensitization enhancement ratios (SER) of sal in three cell lines were 1.16, 1.05 and 1.06, respectively. Conclusions Rradiosensitivity of HNSCC could be effectively enhanced by sal treatment.
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