Activation of Toll-like receptor 3 induces apoptosis of oral squamous carcinoma cells in vitro and in vivo

被引:20
作者
Luo, Qingqiong [2 ]
Hu, Shuiqing [2 ]
Yan, Ming [1 ]
Sun, Zujun [2 ]
Chen, Wantao [1 ]
Chen, Fuxiang [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Dept Oral & Maxillofacial Surg, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Peoples Hosp 9, Dept Clin Labs, Shanghai 200011, Peoples R China
关键词
Toll-like receptor 3; dsRNA-polyinosinic-polycytidilic acid; Oral squamous cell carcinoma; Apoptosis; Interferon-beta; Caspase; 3; NF-KAPPA-B; PROMOTES TUMOR-GROWTH; CANCER CELLS; TLR3; RECOGNITION; RESPONSES; HEAD; PROLIFERATION; EXPRESSION; LIPOSOME;
D O I
10.1016/j.biocel.2012.04.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Toll-like receptors are well known as molecular sensors of pathogen-associated molecular patterns. They control activation of the innate immune response and subsequently shape the adaptive immune response. Recent publications have demonstrated that Toll-like receptors also play important roles in multiple human cancers, yet their function in oral squamous cell carcinoma remains unclear. In this study, we showed that both oral squamous cell carcinoma cell lines and tissues from oral squamous carcinoma patients express relatively high levels of Toll-like receptor 3. We also found that synthetic dsRNA-polyinosinic-polycytidilic acid, a Toll-like receptor 3 ligand, induced apoptosis of oral squamous carcinoma cells mainly via Toll-like receptor 3, through interferon-beta production and activation of caspases 3 and 9. Moreover, in an oral squamous cell carcinoma xenograft mouse model, we demonstrated for the first time that activation of Toll-like receptor 3 inhibited oral squamous cell carcinoma tumor growth in vivo. Therefore, the direct proapoptotic activity of Toll-like receptor 3 in human oral squamous carcinoma cells may make this protein a viable therapeutic target in the treatment of oral squamous cell carcinoma. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1266 / 1275
页数:10
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