scholarly journals Programmed cell death 4 loss increases tumor cell invasion and is regulated by miR-21 in oral squamous cell carcinoma

2010 ◽  
Vol 9 (1) ◽  
pp. 238 ◽  
Author(s):  
Patricia P Reis ◽  
Miranda Tomenson ◽  
Nilva K Cervigne ◽  
Jerry Machado ◽  
Igor Jurisica ◽  
...  
Oncotarget ◽  
2016 ◽  
Vol 8 (5) ◽  
pp. 7729-7739 ◽  
Author(s):  
Yuansheng Duan ◽  
Qinghua He ◽  
Kai Yue ◽  
Haishan Si ◽  
Jiaxin Wang ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Tao Liu ◽  
Qing Liu ◽  
Shutao Zheng ◽  
Xiangpeng Gao ◽  
Mang Lu ◽  
...  

Esophageal cancer (EC) is the eighth most common cancer worldwide and the sixth most common cause of cancer death. There are two main types of EC—squamous cell carcinoma (ESCC) and adenocarcinoma (EAC). Although some advances in the exploration of its possible etiological mechanism were made recently including behaviors and environmental risk factors as well as gene alterations, the molecular mechanism underlying ESCC carcinogenesis and progression remains poorly understood. It has been reported that miR-21 was upregulated in most malignant cancers, the proposed mechanism of which was through suppressing expression of programmed cell death 4 (PDCD4). In present study, it is firstly reported that miR-21 was upregulated in Kazakh’s ESCC and that miR-21 played a negative role in regulating PDCD4 using in situ hybridization (ISH) and luciferase reporter approach. Morever, in model of ESCC xenografted nude mice, miR-21 maybe used as an effective target in the treatment. The present results demonstrated that miR-21 may be a potential therapeutic target in management of ESCC.


2013 ◽  
Vol 182 (2) ◽  
pp. 516-528 ◽  
Author(s):  
Chang-Han Chen ◽  
Hui-Ching Chuang ◽  
Chao-Cheng Huang ◽  
Fu-Min Fang ◽  
Hsuan-Ying Huang ◽  
...  

2018 ◽  
Vol 7 (8) ◽  
pp. 4004-4011 ◽  
Author(s):  
Wu Jingjing ◽  
Guo Wenzheng ◽  
Wen Donghua ◽  
Hou Guangyu ◽  
Zhou Aiping ◽  
...  

2020 ◽  
Vol 111 (4) ◽  
pp. 1113-1123
Author(s):  
Shunichi Sudo ◽  
Hiroshi Kajiya ◽  
Shinji Okano ◽  
Mina Sasaki ◽  
Yuri Katsumata ◽  
...  

Open Medicine ◽  
2020 ◽  
Vol 15 (1) ◽  
pp. 292-301
Author(s):  
Yong-Xin Cui ◽  
Xian-Shuang Su

AbstractObjectiveProgrammed cell death-ligand 1 (PD-L1) expression has been shown to play important roles in various types of cancer. However, the role of PD-L1 expression has not been conclusively reported in patients with oral squamous cell carcinoma (OSCC). Accordingly, in this meta-analysis, we investigated the clinicopathological value of PD-L1 expression in patients with OSCC.MethodsGoogle Scholar, PubMed, EMBASE, and CNKI databases were searched to find relevant studies published through to September 16, 2019. The relationships between PD-L1 expression in patients with OSCC and clinicopathological features were assessed using risk ratio (RR) and 95% confidence intervals (CIs).ResultsSixteen studies including 1989 participants were included. The results indicated that high PD-L1 expression was correlated with sex (RR = 1.28, 95% CI: 1.16–1.42, P < 0.001), N stage (RR = 1.19, 95% CI: 1.06–1.33, P = 0.003), M stage (RR = 1.64, 95% CI: 1.01–2.66, P = 0.044), low differentiation (RR = 1.16, 95% CI: 1.01–1.33, P = 0.034), and human papilloma virus infection (RR = 1.38, 95% CI: 1.14–1.68, P = 0.001), but unrelated to TNM stage or T stage. There was no significant publication bias in the studies included in this analysis.ConclusionsThis meta-analysis revealed that high PD-L1 expression in patients with OSCC was correlated with clinicopathological features. Further large-scale studies are necessary to confirm our results.


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