Evaluation of CERS2 Gene as a Potential Biomarker for Bladder Cancer
Autor: | Rosna Yunus, Aminuddin Baharudin, Umar Ahmad, Soon Choy Chan, Teng Aik Ong, Azad Hassan Abdul Razack, Khatijah Yusoff, Abhi Veerakumarasivam, Ahmed Faris Aldoghachi |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Article Subject Clinical Biochemistry Newcastle disease virus 03 medical and health sciences Inhibitory Concentration 50 0302 clinical medicine Downregulation and upregulation Cell Movement Cell Line Tumor Sphingosine N-Acyltransferase Genetics Biomarkers Tumor Medicine Humans RNA Small Interfering Molecular Biology Regulation of gene expression Oncolytic Virotherapy lcsh:R5-920 Bladder cancer business.industry Tumor Suppressor Proteins Biochemistry (medical) Ceramide synthase 2 Cancer Membrane Proteins General Medicine medicine.disease Oncolytic virus Gene Expression Regulation Neoplastic 030104 developmental biology Phenotype Urinary Bladder Neoplasms Cell culture 030220 oncology & carcinogenesis Cancer research Immunohistochemistry Neoplasm Recurrence Local lcsh:Medicine (General) business Research Article |
Zdroj: | Disease Markers Disease Markers, Vol 2019 (2019) |
ISSN: | 1875-8630 0278-0240 |
Popis: | The ceramide synthase 2 (CERS2) gene has been linked to tumour recurrence and invasion in many different types of cancers including bladder cancer. In this study, the expression levels of CERS2 in bladder cancer cell lines were analysed using qRT-PCR and the protein expression in clinical bladder cancer histopathological specimens were examined via immunohistochemistry. The potential utility of CERS2 as a predictive biomarker of response to oncolytic virotherapy was assessed by correlating the CERS2 mRNA expression to IC50 values of cells treated with the Newcastle disease virus (NDV), AF2240 strain. This study demonstrates that CERS2 is differentially expressed in different types of bladder cancer cell lines and that the siRNA-mediated downregulation of the expression of CERS2 reduces the migratory potential of UMUC1 bladder cancer cells. However, there were no significant correlations between the expression levels of the CERS2 protein with bladder cancer grade/stage or between the IC50 values of cells treated with NDV and CERS2 expression. Although the utility of CERS2 expression may be limited, its potential as an antimigration cancer therapeutic should be further examined. |
Databáze: | OpenAIRE |
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