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1.
Arch Toxicol ; 86(2): 195-203, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21892705

RESUMEN

Currently, twelve validated genetic variants have been identified that are associated with urinary bladder cancer (UBC) risk. However, those validated variants explain only 5-10% of the overall inherited risk. In addition, there are more than 100 published polymorphisms still awaiting validation or disproval. A particularly promising of the latter unconfirmed polymorphisms is rs2854744 that recently has been published to be associated with UBC risk. The [A] allele of rs2854744 has been reported to be associated with a higher promoter activity of the insulin-like growth factor-binding protein-3 (IGFBP3) gene, which may lead to increased IGFBP-3 plasma levels and cancer risk. Therefore, we investigated the association of rs2854744 with UBC in the IfADo case-control series consisting of 1,450 cases and 1,725 controls from Germany, Hungary, Venezuela and Pakistan. No significant association of rs2854744 with UBC risk was obtained (all study groups combined: unadjusted P = 0.4446; adjusted for age, gender and smoking habits P = 0.6510), besides a small effect of the [A] allele in the Pakistani study group opposed to the original findings (unadjusted P = 0.0508, odds ratio (OR) = 1.43 for the multiplicative model) that diminished after adjustment for age, gender and smoking habits (P = 0.7871; OR = 0.93). Associations of rs2854744 with occupational exposure to urinary bladder carcinogens and smoking habits were also not present. A meta-analysis of all available case-control series including the original discovery study resulted in an OR of 1.00 (P = 0.9562). In conclusion, we could not confirm the recently published hypothesis that rs2854744 in the IGFBP3 gene is associated with UBC risk.


Asunto(s)
Proteína 3 de Unión a Factor de Crecimiento Similar a la Insulina/genética , Neoplasias de la Vejiga Urinaria/genética , Adulto , Anciano , Anciano de 80 o más Años , Estudios de Casos y Controles , Femenino , Predisposición Genética a la Enfermedad/etnología , Alemania , Humanos , Hungría , Masculino , Persona de Mediana Edad , Pakistán , Polimorfismo de Nucleótido Simple , Neoplasias de la Vejiga Urinaria/etnología , Venezuela
2.
Arch Toxicol ; 84(12): 967-78, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21063684

RESUMEN

Single nucleotide polymorphism (SNP) rs710521[A], located near TP63 on chromosome 3q28, was identified to be significantly associated with increased bladder cancer risk. To investigate the association of rs710521[A] and bladder cancer by new data and by meta-analysis including all published data, rs710521 was studied in 1,425 bladder cancer cases and 1,740 controls that had not been included in previous studies. Blood samples were collected from 1995 to 2010 in Germany (n = 948/1,258), Hungary (n = 262/65), Venezuela (n = 112/190) and Pakistan (n = 103/227) supplemented by a meta-analysis of 5,695 cases and 40,187 controls. Detection of a A/G substitution (rs710521) on chromosome 3q28, position 191128627 was done via fast real-time polymerase chain reaction (rt-PCR). Rs710521[A] is associated with increased risk in the unadjusted analysis (OR = 1.21; 95% Cl = 1.04-1.40; P = 0.011) and in the recessive model adjusted for age, gender, smoking habits and ethnicity (OR = 1.23; 95% Cl = 1.05-1.44; P = 0.010). No difference between individuals occupationally exposed versus not occupationally exposed to urinary bladder carcinogens was observed concerning the relevance of rs710521[A]. Similarly, rs710521[A] did not confer different susceptibility in smokers and non-smokers. Performing a meta-analysis of 5,695 cases and 40,187 controls including all published studies on rs710521, a convincing association with bladder cancer risk was obtained (OR = 1.18; 95% Cl = 1.12-1.25; P < 0.0001). However, the odds ratio is relatively small.


Asunto(s)
Cromosomas Humanos Par 3 , Genes , Polimorfismo de Nucleótido Simple , Transactivadores/genética , Proteínas Supresoras de Tumor/genética , Neoplasias de la Vejiga Urinaria/genética , Estudios de Casos y Controles , Femenino , Alemania , Humanos , Hungría , Masculino , Oportunidad Relativa , Pakistán , Reacción en Cadena de la Polimerasa , Riesgo , Fumar/efectos adversos , Fumar/genética , Factores de Transcripción , Venezuela
3.
J Pediatr Urol ; 6(3): 282-7, 2010 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-19837635

RESUMEN

INTRODUCTION: Prune belly syndrome (PBS) presents with large-capacity bladders, high compliance and post-void residual volumes. Operative and conservative treatments are controversial. When histologically compared to normal bladder, bladder outlet obstruction results in an up- or down-regulation of adrenoceptors. Our goal was to study the immunoexpression of adrenoceptors in detrusor from patients with PBS. MATERIALS AND METHODS: Bladder domes from PBS patients (n=14) were studied (PBG). For normal controls, bladder specimens were obtained at adult surgery (n=13) (CG1) and at child autopsy (n=5) (CG2). Staining was performed using antibodies to alpha1a, alpha1b, alpha1d and beta3 adrenoceptors. Five to 10 images were captured on an optic microscope with a digital camera and analysed with Photoshop. The immunocyhistochemical index with arbitrary units was calculated and compared. RESULTS: Mean age was 1.28, 64 and 1.41 years for PBG, CG1 and CG2, respectively. The immunohistochemical index with arbitrary units of alpha1a receptors was 0.06 in PBG, 0.16 in CG1 and 0.14 in CG2 (p=0.008); of alpha1b 0.06, 0.06 and 0.07 (p=0.781); and of alpha1d 0.04, 0.04 and 0.05 (p=0.618). Regarding beta3 the respective values were 0.07, 0.14 and 0.10 (p=0.378). CONCLUSION: Our results show a decrease in alpha1a-adrenoceptor immunostaining intensity in detrusor from children with PBS. Further in vitro studies are needed to determine whether these observations are physiologically significant.


Asunto(s)
Anticuerpos/metabolismo , Procesamiento de Imagen Asistido por Computador/métodos , Fotomicrografía/métodos , Síndrome del Abdomen en Ciruela Pasa/inmunología , Receptores Adrenérgicos/biosíntesis , Vejiga Urinaria/metabolismo , Urotelio/metabolismo , Anticuerpos/inmunología , Biomarcadores/metabolismo , Progresión de la Enfermedad , Femenino , Humanos , Inmunohistoquímica , Lactante , Masculino , Persona de Mediana Edad , Síndrome del Abdomen en Ciruela Pasa/complicaciones , Síndrome del Abdomen en Ciruela Pasa/metabolismo , Receptores Adrenérgicos/inmunología , Receptores Adrenérgicos alfa 1/biosíntesis , Receptores Adrenérgicos alfa 1/inmunología , Receptores Adrenérgicos beta 3/biosíntesis , Receptores Adrenérgicos beta 3/inmunología , Estudios Retrospectivos , Obstrucción del Cuello de la Vejiga Urinaria/etiología , Obstrucción del Cuello de la Vejiga Urinaria/inmunología , Obstrucción del Cuello de la Vejiga Urinaria/metabolismo , Urotelio/ultraestructura
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