EIF5A2 predicts outcome in localised invasive bladder cancer and promotes bladder cancer cell aggressiveness in vitro and in vivo

التفاصيل البيبلوغرافية
العنوان: EIF5A2 predicts outcome in localised invasive bladder cancer and promotes bladder cancer cell aggressiveness in vitro and in vivo
المؤلفون: Yujing Fang, Dan Xie, W. M. Zhong, Jianlong Zhang, C. Z. Liang, Jia-Wei Wei, S. Fan, Z. H. Chen, B. Liao, Y. B. Liao, R. H. Wu, H. W. Zhao, J. Z. Cao, J. Pang, B. Li, Dingmei Zhang, Z. T. Tong, Wen Hui Chen, J. Lu, J. H. Luo
المصدر: British Journal of Cancer
بيانات النشر: Nature Publishing Group, 2014.
سنة النشر: 2014
مصطلحات موضوعية: STAT3 Transcription Factor, Cancer Research, Pathology, medicine.medical_specialty, Epithelial-Mesenchymal Transition, Cell, Motility, Mice, Nude, Biology, epithelial–mesenchymal transition, STAT3, Transforming Growth Factor beta1, Mice, In vivo, Cell Movement, Peptide Initiation Factors, TGF-β1, EIF5A2, medicine, Biomarkers, Tumor, Animals, Humans, Neoplasm Invasiveness, Epithelial–mesenchymal transition, Molecular Diagnostics, Cells, Cultured, Retrospective Studies, Gene knockdown, Mice, Inbred BALB C, Bladder cancer, RNA-Binding Proteins, aggressiveness, medicine.disease, Prognosis, Gene Expression Regulation, Neoplastic, medicine.anatomical_structure, Oncology, Urinary Bladder Neoplasms, biology.protein, Cancer research, Immunohistochemistry, bladder cancer, Female
الوصف: Background: EIF5A2, eukaryotic translation initiation factor 5A2, is associated with several human cancers. In this study, we investigated the role of EIF5A2 in the metastatic potential of localised invasive bladder cancer (BC) and its underlying molecular mechanisms were explored. Methods: The expression pattern of EIF5A2 in localised invasive BC was determined by immunohistochemistry. In addition, the function of EIF5A2 in BC and its underlying mechanisms were elucidated with a series of in vitro and in vivo assays. Results: Overexpression of EIF5A2 was an independent predictor for poor metastasis-free survival of localised invasive BC patients treated with radical cystectomy. Knockdown of EIF5A2 inhibited BC cell migratory and invasive capacities in vitro and metastatic potential in vivo and reversed epithelial–mesenchymal transition (EMT), whereas overexpression of EIF5A2 promoted BC cells motility and invasiveness in vitro and metastatic potential in vivo and induced EMT. In addition, we found that EIF5A2 might activate TGF-β1 expression to induce EMT and drive aggressiveness in BC cells. EIF5A2 stabilized STAT3 and stimulated nuclear localisation of STAT3, which resulted in increasing enrichment of STAT3 onto TGF-β1 promoter to enhance the transcription of TGF-β1. Conclusions: EIF5A2 overexpression predicts tumour metastatic potential in patients with localised invasive BC treated with radical cystectomy. Furthermore, EIF5A2 elevated TGF-β1 expression through STAT3 to induce EMT and promotes aggressiveness in BC.
اللغة: English
تدمد: 1532-1827
0007-0920
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68a5cb3d57cb6ff82665a962edbe4a14Test
http://europepmc.org/articles/PMC3974079Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....68a5cb3d57cb6ff82665a962edbe4a14
قاعدة البيانات: OpenAIRE