Quick Search:       Advanced Search
PROX1 promoted the progression of non-small cell lung cancer via epithelial-mesenchymal transition
Received:March 03, 2021  Revised:June 26, 2021  Click here to download the full text
Citation of this paper:GAO Jian,AO Yong-qiang,ZHANG Ling-xian,WANG Shuai,DING Jian-yong,JIANG Jia-hao.PROX1 promoted the progression of non-small cell lung cancer via epithelial-mesenchymal transition[J].Chinese Journal of Clinical Medicine,2021,28(5):802-807
Hits: 1148
Download times: 272
Author NameAffiliationE-mail
GAO Jian Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China  
AO Yong-qiang Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China  
ZHANG Ling-xian Department of Cardiothoracic Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China  
WANG Shuai Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China  
DING Jian-yong Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China ding.jianyong@zs-hospital.sh.cn 
JIANG Jia-hao Department of Thoracic Surgery, Zhongshan Hospital, Fudan University, Shanghai 200032, China jiang.jiahao@zs-hospital.sh.cn 
Abstract:Objective: To explore the function and mechanism of PROX1 in non-small cell lung cancer (NSCLC). Methods: The tissue micro-array containing 108 NSCLC tissues was used to explore the relationship between the expression of PROX1 and the prognosis of NSCLC patients. Western blot and quantitative real-time polymerase chain reaction (qRT-PCR) were used to detect the expression of PROX1 in the NSCLC cell line and detect the biomarkers of epithelial-to-mesenchymal transition (EMT). Moreover, the CCK8 and Transwell assay was used to detect the proliferation, invasion, and migration ability of the NSCLC cell line. Results: The expression of PROX1 was upregulated in NSCLC. The expression of PROX1 was closely associated with tumor size and lymphocyte metastasis (P=0.003 and 0.042). The NSCLC patients in the PROX1 high group had a higher recurrence rate and lower survival rate than in the PROX1 low group with the five-year recurrence rate (70.9% vs 50.9%, P=0.005) and the five-year survival rate (49.1% vs 66%, P=0.016). The CCK-8 and Transwell assays showed that the proliferation, invasion, and migration of NSCLC were significantly reduced after the knockdown of PROX1(P<0.01、P<0.05). In terms of mechanism, the knockdown of PROX1 led to the upregulation of E-cadherin and reduction of vimentin(P<0.001). Conclusions: The upregulation of PROX1 contributes to the progression of NSCLC through EMT and it can be a potential biomarker for the prognosis of NSCLC.
keywords:Prospero-related homeobox 1  non-small cell lung cancer  epithelial-mesenchymal transition  prognosis
HTML  View Full Text  View/Add Comment  Download reader