Expression and Functional Analysis of Toll-like Receptor 4 in Human Cervical Carcinoma

被引:34
|
作者
Wang, Yongjun [1 ]
Weng, Yanjie [2 ]
Shi, Ying [2 ]
Xia, Xi [3 ]
Wang, Shixuan [2 ]
Duan, Hua [1 ]
机构
[1] Capital Med Univ, Beijing Obstet Gynecol Hosp, Gynecol Minimal Invas Ctr, Beijing 100006, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Canc Biol Res Ctr, Wuhan 430030, Hubei, Peoples R China
[3] Affiliated Shenzhen Nanshan Hosp, Dept Gynecol & Obstet, Guangdong Med Coll, Shenzhen 518052, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Toll-like receptor 4; Cervical cancer; Cervical intraepithelial neoplasia; HPV; Lipopolysaccharide; EPITHELIAL-CELLS; TUMOR-CELLS; TLR4; PROMOTES; INNATE; MICROENVIRONMENT; ACTIVATION; INDUCTION; CYTOKINES; RESPONSES;
D O I
10.1007/s00232-014-9675-7
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 expressed in human immune cells and many tumors, but the role of toll-like receptor 4 (TLR4) in the development of tumors is controversial. We demonstrated the expression, distribution, and functional activity of TLR4 in tissues of normal cervix, cervical intraepithelial neoplasia (CIN), invasion cervical cancers (ICC), and different human papillomavirus (HPV)-infected cervical cancer cells. The results showed that TLR4 expression was in accordance with the histopathological grade: higher in ICC than in CIN, and low in normal cervical tissues and malignant cervical stroma. Expression was higher in SiHa (HPV16+) than in HeLa (HPV18+) cells, but was not observed in C33A (HPV-) cells. After treatment with its agonist, lipopolysaccharide (LPS), the expression levels of TLR4 was increased and apoptosis resistance was induced in SiHa cells, but not in HeLa or C33A cells. Meanwhile, LPS treatment did not alter the cell cycle distribution in SiHa cells. The mechanism of apoptosis resistance may be related to HPV16 infection and not correlated with the cell cycle distribution. Targeting TLR4 in combination with traditional drug treatment may serve as a novel strategy for more effectively killing cancer cells.
引用
收藏
页码:591 / 599
页数:9
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