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TFIIB-Related Factor 2 Is Associated with Poor Prognosis of Nonsmall Cell Lung Cancer Patients through Promoting Tumor Epithelial-Mesenchymal Transition
Author(s) -
Yu Tian,
Ming Lü,
Weiming Yue,
Lin Li,
Shuhai Li,
Cun Gao,
Libo Si,
Lei Qi,
Wensi Hu,
Hui Tian
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/530786
Subject(s) - epithelial–mesenchymal transition , gene knockdown , cancer research , mesenchymal stem cell , lung cancer , cadherin , medicine , lung , immunohistochemistry , snail , transition (genetics) , vimentin , oncology , pathology , biology , cancer , cell , metastasis , cell culture , gene , ecology , biochemistry , genetics
In this study, we found that increased BRF2 protein expression was prevalent in NSCLC. Overexpression of BRF2 correlated with abnormal expression of E-cadherin, N-cadherin, and snail. Additionally, expression of BRF2 was found to be an independent prognostic factor in NSCLC patients. Furthermore, we showed that targeted knockdown of BRF2 expression could inhibit the migratory and invasive abilities of NSCLC cells and induced loss of the epithelial-mesenchymal transition of NSCLC cells. These results suggested that BRF2 overexpression in tumor tissues is significantly associated with the poor prognosis of NSCLC patients through promoting epithelial-mesenchymal transition (EMT) program.

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