Axon guidance molecule Semaphorin3A is a novel tumor suppressor in head and neck squamous cell carcinoma

被引:22
作者
Wang, Zhao [1 ,2 ]
Chen, Jie [1 ,2 ]
Zhang, Wei [1 ,3 ]
Zheng, Yang [1 ,2 ]
Wang, Zilu [1 ]
Liu, Laikui [1 ]
Wu, Heming [1 ,2 ]
Ye, Jinhai [1 ,2 ]
Zhang, Wei [1 ,3 ]
Qi, Bing [3 ]
Wu, Yunong [1 ,2 ]
Song, Xiaomeng [1 ,2 ]
机构
[1] Nanjing Med Univ, Jiangsu Key Lab Oral Dis, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp Stomatol, Dept Oral & Maxillofacial Surg, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp Stomatol, Dept Oral Pathol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Semaphorin3A; HNSCC; apoptosis; NF-kappaB; Snail; EPITHELIAL-MESENCHYMAL TRANSITION; NF-KAPPA-B; CLASS-3; SEMAPHORINS; TONGUE CANCER; EXPRESSION; METASTASIS; 3A; ANGIOGENESIS; RECEPTORS; GROWTH;
D O I
10.18632/oncotarget.6831
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Semaphorin3A (SEMA3A), an axon guidance molecule in the nervous system, plays an inhibitory role in oncogenesis. Here, we investigated the expression pattern and biological roles of SEMA3A in head and neck squamous cell carcinoma (HNSCC) by gain-of-function assays using adenovirus transfection and recombinant human SEMA3A protein. In addition, we explored the therapeutic efficacy of SEMA3A against HNSCC in vivo. We found that lower expression of SEMA3A correlated with shorter overall survival and had independent prognostic importance in patients with HNSCC. Both genetic and recombinant SEMA3A protein inhibited cell proliferation and colony formation and induced apoptosis, accompanied by decreased cyclin E, cyclin D, CDK2, CDK4 and CDK6 and increased P21, P27, activated caspase-5 and caspase-7. Moreover, over-expression of SEMA3A suppressed migration, invasion and epithelial-to-mesenchymal transition due in part to the inhibition of NF-kappa B and SNAI2 in HNSCC cell lines. Furthermore, intratumoral SEMA3A delivery significantly stagnated tumor growth in a xenograft model. Taken together, our results indicate that SEMA3A serves as a tumor suppressor during HNSCC tumorigenesis and a new target for the treatment of HNSCC.
引用
收藏
页码:6048 / 6062
页数:15
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