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1.
J Infect Dev Ctries ; 15(7): 997-1003, 2021 07 31.
Artículo en Inglés | MEDLINE | ID: mdl-34343125

RESUMEN

INTRODUCTION: Several micro ribonucleic acids (miRNAs) are deregulated in hepatocellular carcinoma (HCC). Others are linked to clinical pathological features of HCC. The goal of this study was to investigate whether miRNA-21 and miRNA-215 gene expression could be used as a non-invasive diagnostic tool to diagnose HCC. METHODOLOGY: The gene expression of mature miRNA -21 and miRNA -215 in serum was analysed retrospectively using singleplex TaqMan two-step stem-loop quantitative real-time reverse-transcription PCR in 40 patients with HCC, 40 with chronic hepatitis C virus (HCV) with cirrhosis and 40 apparently healthy controls. RESULTS: Expression of miRNA -21 was significantly more down regulated in patients with HCC than in those with non-cirrhotic HCV (P = 0.007; odds ratio = 5; 95% confidence interval 1.6-15.4). The receiver operating curve analysis of the ability of miRNA-21 expression to discriminate between HCC and non-cirrhotic HCV revealed an area under the curve of 0.712 with 70% sensitivity and 68% specificity at a cut-off of ≤ 1.4468. Thus, the expression level of miRNA -21 could discriminate HCC from non-cirrhotic HCV. Significant positive correlation was observed between expression levels of microRNA-21 and miRNA -215 (r = 0.783, p < 0.001), but no association was observed between expression level of miR-215 and HCC or chronic HCV (p = 0.474). CONCLUSIONS: MiRNA-21 may be a useful, non-invasive tool for diagnosing HCC. Non-cirrhotic HCV patients have five times the risk of developing HCC when the miRNA -21 level ≤ 1.4468.


Asunto(s)
Carcinoma Hepatocelular/diagnóstico , Hepatitis C/complicaciones , Neoplasias Hepáticas/diagnóstico , MicroARNs/sangre , Adulto , Carcinoma Hepatocelular/virología , Estudios de Casos y Controles , Regulación hacia Abajo , Femenino , Expresión Génica , Regulación Viral de la Expresión Génica , Hepatitis C/diagnóstico , Humanos , Neoplasias Hepáticas/virología , Masculino , MicroARNs/genética , Persona de Mediana Edad , Curva ROC
2.
Int J Occup Environ Med ; 10(3): 124-136, 2019 07.
Artículo en Inglés | MEDLINE | ID: mdl-31325295

RESUMEN

BACKGROUND: Coke oven workers are exposed to polycyclic aromatic hydrocarbons (PAHs) with possible genotoxicity and carcinogenicity. Metabolizing enzymes genes and DNA repair genes are suspected to be correlated with the level of DNA damage. They may contribute to variable individual sensitivity to DNA damage induced by PAHs exposure at workplace. OBJECTIVE: To investigate the relationship between biomarkers of PAHs: 1-hydroxypyrene (1-OHP), DNA adducts, and 8-hydroxy-2-deoxyguanosine (8-OHdG) in coke oven workers, and to assess the role of cytochrome P2E1 (CYP2E1) gene expression and DNA repairing gene (XRCC1) polymorphism in detecting workers at risk. METHODS: 85 exposed workers and 85 unexposed controls were enrolled into this study. Urinary 1-OHP, 8-OHdG, and BPDE-DNA adduct were measured. CYP2E1 gene expression and genotyping of XRCC1 399 Arg/Gln were evaluated by real-time PCR. RESULTS: The median urinary 1-OHP levels (6.3 µmol/mol creatinine), urinary 8-OHdG (7.9 ng/mg creatinine), DNA adducts (6.7 ng/µg DNA) in the exposed group were significantly higher than those in the unexposed group. Carriers of the variant allele (Gln) of XRCC1 had the highest levels of 1-OHP, DNA adducts and 8-OHdG, and the lowest level of CYP2E1 gene expression. In exposed workers, significant positive correlations were found between 1-OHP level and each of the work duration, 8-OHdG, and DNA adducts levels. There was a significant negative correlation between 1-OHP level and CYP2E1 gene expression. Work duration and CYP2E1 gene expression were predictors of DNA adducts level; 1-OHP level and work duration were predictors of urinary 8-OHdG level. CONCLUSION: Workers with higher exposure to PAH were more prone to oxidative DNA damage and cancer development. DNA adducts level reflects the balance between their production by CYP2E1 and elimination by XRCC1 gene.


Asunto(s)
Citocromo P-450 CYP2E1/genética , Aductos de ADN/genética , Desoxiguanosina/análogos & derivados , Monitoreo del Ambiente/métodos , Exposición Profesional/análisis , Pirenos/orina , Proteína 1 de Reparación por Escisión del Grupo de Complementación Cruzada de las Lesiones por Rayos X/genética , 7,8-Dihidro-7,8-dihidroxibenzo(a)pireno 9,10-óxido , 8-Hidroxi-2'-Desoxicoguanosina , Adulto , Biomarcadores/orina , Coque , Citocromo P-450 CYP2E1/biosíntesis , Aductos de ADN/orina , Daño del ADN/efectos de los fármacos , Reparación del ADN/genética , Desoxiguanosina/orina , Egipto , Humanos , Masculino , Persona de Mediana Edad , Hidrocarburos Policíclicos Aromáticos/orina , Polimorfismo Genético , Medición de Riesgo , Proteína 1 de Reparación por Escisión del Grupo de Complementación Cruzada de las Lesiones por Rayos X/biosíntesis , Adulto Joven
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