Latent Membrane Protein 1 Antibody Inhibits Cell Migration, Invasion and Epithelial-Mesenchymal Transition of Nasopharyngeal Carcinoma Stem Cell via Regulating Wnt/β-Catenin Signaling Pathway

被引:0
|
作者
Zhang, Dawei [1 ]
Xiong, Lin [2 ]
Li, Liang [1 ]
Chen, Yuan [1 ]
Tang, Xiaojun [3 ]
Tang, Qi [4 ]
Mao, Yuan [5 ]
Ming, Hao [1 ]
Chen, Zhi [1 ]
Du, Yinjuan [1 ]
Wang, Yang [1 ]
Chen, Renjie [1 ]
Zhu, Jin [6 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 2, Dept Otolaryngol Head & Neck Surg, 121 Jiang Jia Yuan, Nanjing 210011, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 2, Dept Pathol, 121 Jiang Jia Yuan, Nanjing 210011, Peoples R China
[3] Nanjing Univ, Med Sch, Affiliated Drum Tower Hosp, Dept Rheumatol & Immunol, Nanjing 210008, Peoples R China
[4] Nanjing Med Univ, Minist Hlth, Key Lab Antibody Tech, 101 Longmian Ave, Nanjing 211166, Peoples R China
[5] Jiangsu Prov Geriatr Hosp, Dept Geriatr Lung Canc Lab, Dept Hematol & Oncol, 65 Jiangsu Rd, Nanjing 210029, Peoples R China
[6] Huadong Med Inst Biotech, 293 Zhongshan Dong Rd, Nanjing 210002, Peoples R China
关键词
Nasopharyngeal Carcinoma; Latent Membrane Protein 1; Epithelial-Mesenchymal Transition; Migration; Invasion; NF-KAPPA-B; LMP1; METASTASIS; CANCER; EXPRESSION; APOPTOSIS;
D O I
10.1166/jbt.2020.2361
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Objective: In order to investigate the effects of LMP1-Fab antibody on Nasopharyngeal carcinoma (NPC) cancer stem cells (CSCs). Methods/Results: Methods were performed to study the effects of LMP1-Fab antibody on NPC CSCs in vivo and in vitro, for example, transwell chamber assay, wound healing assay, western blot assay, quantitative real-time PCR assay animal experiments, animal fluorescence imaging, H&E staining, immunohistochemistry. We identified that LMP1 activated the migration and invasion of NPC. Whereas the LMP1-Fab antibody inhibited cell invasion, epithelial-mesenchymal transition (EMT) and migration of NPC CSCs in LMP1+ HNE2 cells. Furthermore, LMP1-Fab antibody significantly increased the expression of E-cadherin, and reduced the expressions of vimentin, N-cadherin and Slug in LMP1+ HNE2 CSCs cells. Mechanistically, LMP1-Fab antibody inhibited lung and liver metastasis by regulating the wnt/beta-catenin pathway in the nude mice. Conclusion: These results suggested that the novel antibody-targeting LMP1 is likely to be a potential strategy for the treatment of NPC.
引用
收藏
页码:930 / 938
页数:9
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