CEACAM5 stimulates the progression of non-small-cell lung cancer by promoting cell proliferation and migration

被引:35
作者
Zhang, Xinwen [1 ]
Han, Xingbao [2 ]
Zuo, Pengli [3 ]
Zhang, Xiuying [4 ]
Xu, Hongbang [5 ]
机构
[1] Linyi Cent Hosp, Dept Gen Practice, Linyi, Shandong, Peoples R China
[2] Linyi Cent Hosp, Dept Urol, Linyi, Shandong, Peoples R China
[3] Linyi Cent Hosp, Cent Lab, Linyi, Shandong, Peoples R China
[4] Linyi Cent Hosp, Dept Clin Lab, Linyi, Shandong, Peoples R China
[5] Linyi Cent Hosp, Dept Resp Med, 17 Jiankang Rd, Linyi 276400, Shandong, Peoples R China
关键词
Non-small-cell lung cancer; CEA-related cell adhesion molecule 5; proliferation; migration; therapeutic target; p38-Smad2; 3; signaling; tumorigenesis; SIGNALING PATHWAY; EXPRESSION; FAMILY; IDENTIFICATION; PROGNOSIS;
D O I
10.1177/0300060520959478
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective To detect the expression of CEA-related cell adhesion molecule 5 (CEACAM5) in non-small-cell lung cancer (NSCLC) and explore its function in the progression and development of NSCLC. Methods qRT-PCR and immunohistochemistry were performed to detect CEACAM5 expression in human NSCLC tissues and cell lines. The correlation between CEACAM5 expression and the clinicopathological features of patients with NSCLC was also investigated. MTT, colony formation, wound healing, and immunoblot assays were performed to detect the functions of CEACAM5 in NSCLC cellsin vitro, and immunoblotting was used to detect the effects of CEACAM5 on p38-Smad2/3 signaling. Results CEACAM5 expression was elevated in human NSCLC tissues and cells. We further found that CEACAM expression was correlated with clinicopathological features including T division, lymph invasion, and histological grade in patients with NSCLC. Thein vitroassays confirmed that CEACAM5 depletion inhibited the proliferation and migration of NSCLC cells by activating p38-Smad2/3 signaling. We verified the involvement of CEACAM5 in the suppression of NSCLC tumor growth in mice. Conclusion CEACAM5 stimulated the progression of NSCLC by promoting cell proliferation and migrationin vitroandin vivo. CEACAM5 may serve as a potential therapeutic target for the treatment of NSCLC.
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页数:15
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