Glycidamide Promotes the Growth and Migratory Ability of Prostate Cancer Cells by Changing the Protein Expression of Cell Cycle Regulators and Epithelial-to-Mesenchymal Transition (EMT)-Associated Proteins with Prognostic Relevance
Autor: | Chi Chen Huang, Wen Fu T. Lai, Titus Ime Ekanem, Kuen Haur Lee, Ding Yen Lin, Ming Heng Wu |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Male
Epithelial-Mesenchymal Transition Cell Survival Regulator Cell Cycle Proteins Kaplan-Meier Estimate Biology gene signature Catalysis Article Malignant transformation lcsh:Chemistry Inorganic Chemistry Prostate cancer Cell Movement Cell Line Tumor medicine Biomarkers Tumor Humans Epithelial–mesenchymal transition cell cycle regulator Physical and Theoretical Chemistry lcsh:QH301-705.5 Molecular Biology Spectroscopy Gene Expression Profiling Organic Chemistry Cell Cycle fungi EMT Prostatic Neoplasms food and beverages General Medicine Cell cycle Gene signature medicine.disease prostate cancer Computer Science Applications Gene Expression Regulation Neoplastic SNAI2 lcsh:Biology (General) lcsh:QD1-999 glycidamide Cancer cell Cancer research Epoxy Compounds prognosis Transcriptome Signal Transduction |
Zdroj: | International Journal of Molecular Sciences Volume 20 Issue 9 International Journal of Molecular Sciences, Vol 20, Iss 9, p 2199 (2019) |
ISSN: | 1422-0067 |
DOI: | 10.3390/ijms20092199 |
Popis: | Acrylamide (AA) and glycidamide (GA) can be produced in carbohydrate-rich food when heated at a high temperature, which can induce a malignant transformation. It has been demonstrated that GA is more mutagenic than AA. It has been shown that the proliferation rate of some cancer cells are increased by treatment with GA however, the exact genes that are induced by GA in most cancer cells are not clear. In the present study, we demonstrated that GA promotes the growth of prostate cancer cells through induced protein expression of the cell cycle regulator. In addition, we also found that GA promoted the migratory ability of prostate cancer cells through induced epithelial-to-mesenchymal transition (EMT)-associated protein expression. In order to understand the potential prognostic relevance of GA-mediated regulators of the cell cycle and EMT, we present a three-gene signature to evaluate the prognosis of prostate cancer patients. Further investigations suggested that the three-gene signature (CDK4, TWIST1 and SNAI2) predicted the chances of survival better than any of the three genes alone for the first time. In conclusion, we suggested that the three-gene signature model can act as marker of GA exposure. Hence, this multi-gene panel may serve as a promising outcome predictor and potential therapeutic target in prostate cancer patients. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |