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1.
Rev Epidemiol Sante Publique ; 69(6): 329-336, 2021 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-34629211

RESUMEN

BACKGROUND: Morbidity and mortality associated with prostate cancer in a given geographic area might be related to the level of socioeconomic deprivation. The Somme area (a region of northern France) is considered economically disadvantaged, with major territorial disparities. The aim of this study was to assess the impact of the socioeconomic level on prostate cancer, using data from a population-based cancer registry. METHODS: The source of data on cases of prostate cancer between 2006 and 2010 was the Somme cancer registry (Amiens, France). Socioeconomic status was measured according to the European Deprivation Index (EDI), which was used to classify each geographical "IRIS" unit (the smallest sub-municipal geographical entity for which French census data are available) according to its level of social deprivation. For spatial analysis, we considered a hierarchical generalized linear model. RESULTS: In the spatial analysis, prostate cancer incidence was higher in the less disadvantaged areas and treatment frequency with curative intent was lower in the most disadvantaged areas. Cancer aggressiveness and mortality were higher in the most disadvantaged areas: relative risk (RR) = 1.36; 95% CI: [1.09; 1.73] and RR=3.09 [1.70; 5.59], respectively. CONCLUSION: Our results evidenced a significant association between socioeconomic deprivation and prostate cancer, with worse outcomes among men with the lowest socioeconomic status.


Asunto(s)
Neoplasias de la Próstata , Disparidades en el Estado de Salud , Humanos , Incidencia , Masculino , Neoplasias de la Próstata/epidemiología , Neoplasias de la Próstata/terapia , Sistema de Registros , Clase Social , Factores Socioeconómicos , Análisis Espacial
2.
Anim Reprod Sci ; 122(3-4): 328-34, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21075566

RESUMEN

In seasonal breeding species, the gene encoding for the melatonin MT(1) receptor (oMT(1)) is highly polymorphic and numerous data have reported the existence of an association between an allele of the receptor and a marked expression of the seasonality of reproduction in ewes. This allele called "m" (previously named "-" allele) carries a mutation leading to the absence of a MnlI restriction site as opposed to the "M" allele (previously named "+" allele) carrying the MnlI restriction site (previously "+" allele). This allows the determination of the three genotypes "M/M" (+/+), "M/m" (+/-) and "m/m" (-/-). This mutation is conservative and could therefore not be causal. However, it is associated with another mutation introducing the change of a valine to an isoleucine in the fifth transmembrane domain of the receptor. Homozygous "M/M" and "m/m" animals consequently express structurally different receptors respectively named oMT(1) Val(220) and oMT(1) Ile(220). The objective of this study was to test whether these polymorphic variants are functionally different. To achieve this goal, we characterized the binding properties and the transduction pathways associated with both variants of the receptors. Using a pharmacological approach, no variation in binding parameters between the two receptors when transiently expressed in COS-7. In stably transfected HEK293 cells, significant differences were detected in the inhibition of cAMP production whereas receptors internalization processes were not different. In conclusion, the possibility that subtle alterations induced by the non conservative mutation in "m/m" animals might modify the perception of the melatoninergic signal is discussed in the context of melatonin action.


Asunto(s)
Polimorfismo Genético/fisiología , Receptor de Melatonina MT1/genética , Reproducción/genética , Estaciones del Año , Ovinos/genética , Ovinos/fisiología , Alelos , Animales , Cruzamiento , Células COS , Chlorocebus aethiops , AMP Cíclico/biosíntesis , Femenino , Expresión Génica , Genotipo , Células HEK293 , Humanos , Radioisótopos de Yodo , Melatonina/metabolismo , Receptor de Melatonina MT1/metabolismo , Transfección
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