Toll-like receptor 7 agonist, Imiquimod, inhibits oral squamous carcinoma cells through apoptosis and necrosis

被引:42
作者
Ahn, Mee-Young [2 ,3 ]
Kwon, Seong-Min [2 ,3 ]
Cheong, Hak Hyun [2 ,3 ]
Park, Jong-Hwan [4 ]
Lee, Jun [5 ]
Min, Seung-Ki [5 ]
Ahn, Sang-Gun [2 ,3 ]
Yoon, Jung-Hoon [1 ]
机构
[1] Wonkwang Univ, Dept Oral & Maxillofacial Pathol, Coll Dent,Wonkwang Bone Regenerat Res Inst, Daejeon Dent Hosp, Taejon 302120, South Korea
[2] Chosun Univ, Dept Pathol, Kwangju, South Korea
[3] Chosun Univ, Res Ctr Oral Dis Regulat Aged, Sch Dent, Kwangju, South Korea
[4] Konyang Univ, Dept Biochem, Coll Med, Taejon, South Korea
[5] Wonkwang Univ, Dept Oral & Maxillofacial Surg, Coll Dent,Wonkwang Bone Regenerat Res Inst, Daejeon Dent Hosp, Taejon 302120, South Korea
基金
新加坡国家研究基金会;
关键词
apoptosis; imiquimod; necrosis; oral sqaumous cell carcinoma; toll-like receptor 7; CANCER-THERAPY; INFLAMMATION; RECOGNITION; HEPATOCYTES; INTERFERON; INDUCTION; AUTOPHAGY; DEATH; CREAM; HMGB1;
D O I
10.1111/j.1600-0714.2012.01158.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
J Oral Pathol Med (2012) 41: 540546 Background: Toll-like receptor (TLR) agonists have anticancer effect by inducing apoptosis or activating immune cells. In this study, we investigated whether imiquimod, TLR7 agonist, inhibits the proliferation of oral cancer cells. Methods: Toll-like receptor 7 expression and IL-6/8 production by imiquimod were examined using RT-PCR and Enzyme-linked immunosorbent assay, respectively. Cell viability was examined by MTT assay. To examine apoptotic cell death, Annexin V/PI staining for flow cytometry and Western blot analysis were performed. Necrotic cell death was determined by leakage of lactate dehydrogenase (LDH), HMGB1, and PI staining in imiquimod-treated oral squamous cell carcinoma (OSCC) cells. Results: Toll-like receptor7 mRNA was expressed in OSCC cells. Imiquimod induced IL-6 and IL-8 production in OSCC cells, suggesting the functional expression of TLR7. Imiquimod inhibited cells proliferation in a dose-dependent manner. The ratio of annexin V-positive cells and cleaved caspase-3/7 was increased by imiquimod treatment in OSCC cells, suggesting that imiquimod-induced cell death in OSCC cells may be owing to apoptosis. In addition, LDH secretion and PI staining were detected in OSCC cells treated with imiquimod, showing that imiquimod also induced necrotic cell death in the OSCC cells. Conclusions: Imiquimod inhibited effectively the growth of OSCC cells by inducing apoptosis and necrosis.
引用
收藏
页码:540 / 546
页数:7
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