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1.
Pesqui. vet. bras ; 39(1): 40-46, Jan. 2019. tab, ilus
Article in English | LILACS, VETINDEX | ID: biblio-990239

ABSTRACT

Canine prostate gland is a hormonal dependent organ and its imbalance of estrogen and androgen receptor expressions are directly associated with the development of different diseases. Due to the lack of information regarding the behavior of the aforementioned receptors in canine prostate cancer (PC), this study aimed to identify estrogen receptor alpha (ERα), androgen receptor (AR), Ki67 and phosphatase and tensin homolog (PTEN) protein expressions in canine PC by immunohistochemistry. We found nuclear expression of ERα and AR in the epithelial cells of normal canine samples and a loss of protein expression in PC samples. Normal samples showed Ki67 expression in a few basal cells and the PC samples showed the highest mean of positive cells (253.1). Canine prostate cancer showed a high proliferative index, which was associated with independence of hormonal actuation. PTEN showed positive nuclear and cytoplasmic expression in normal canine samples and a loss in PC. Loss of ERα, AR and PTEN indicated that canine PC exhibits the same immunohistochemical phenotype as in human patients with PC resistant to hormonal therapy. Therefore, canine PC should be considered as a model to study human PC resistant to hormonal therapy.(AU)


A glândula prostática canina é um órgão dependente de hormônio, e o desequilíbrio na expressão dos receptores de estrógeno e andrógeno estão diretamente associados com o desenvolvimento de diferentes doenças. Devido à falta de informação sobre o comportamento desses receptores no câncer prostático canino (PC), este estudo tem por objetivo identificar a expressão proteica através da técnica de imuno-histoquímica do receptor de estrógeno alfa (REα), receptor de andrógeno (RA), Ki67 e fosfatase e tensina homóloga (PTEN). Foi encontrado nas células epiteliais prostáticas normais caninas a expressão nuclear de REα e RA, e perda de expressão proteica nas amostras de PC. As amostras normais apresentaram expressão de Ki67 em poucas células basais e as amostras de PC apresentaram a maior média de células positivas (253,1). O câncer de próstata canino apresentou uma taxa alta de proliferação, o qual foi associado com a atuação independente de hormônio. As amostras de próstatas caninas normais revelaram marcação nuclear e citoplasmática da proteína PTEN e perda nas amostras de PC. A perda de REα, RA e PTEN indicam que as amostras de PC exibem o mesmo fenótipo imuno-histoquímico de pacientes humanos com câncer prostático resistente a terapia hormonal. Sendo assim, o PC canino deve ser considerado um modelo para estudos de câncer prostático humano resistente a terapia hormonal.(AU)


Subject(s)
Animals , Dogs , Prostate/pathology , Prostatic Hyperplasia/veterinary , Prostatic Neoplasms/veterinary , Prostatic Intraepithelial Neoplasia/veterinary , Dogs , Receptors, Androgen , Receptors, Cytoplasmic and Nuclear , Estrogen Receptor alpha , Disease Models, Animal , Prostatic Neoplasms, Castration-Resistant/veterinary
2.
Int. j. morphol ; 32(3): 1120-1124, Sept. 2014. ilus
Article in Spanish | LILACS | ID: lil-728320

ABSTRACT

La asociación de factores genéticos, nutricionales y ambientales afecta directamente la fertilidad de las ovejas sin embargo en condiciones de similitud ambiental, la raza es un factor determinante existiendo razas de alta fertilidad como por ejemplo Texel y Suffolk y otras de fertilidad estándar tales como Romney y Criolla Araucana. La fertilidad es modulada por las hormonas sexuales que actúan mediante la unión a receptores específicos. En ovinos el receptor de estrógeno alfa (ER-a) esta ampliamente distribuido en el sistema reproductivo y es responsable de la modulación de varios mecanismos asociados con la función del sistema reproductivo. Un factor posiblemente relacionado con la diferencia en la fertilidad entre razas de ovinos, es el nivel de expresión diferencial de estos receptores en el sistema reproductivo. En el presente estudio se realizo una comparación cuantitativa de la expresión inmunohistoquímica de ER-a se llevó en el endometrio de ovejas prepúberes de ovejas de alta fertilidad (Texel) y de fertilidad estándar (Araucana), mediante la medición de la densidad óptica integrada de la señal inmunohistoquímica en áreas específicas del endometrio. Los resultados indican una diferencia significativa entre la expresión del ER-a a favor de ovejas de raza Texel en todas las áreas de la raza del endometrio de ovejas prepúberes evaluadas. Esta expresión diferencial sugiere una posible relación entre la intensidad de la expresión de ER-a y la fertilidad en las razas ovinas estudiadas en este trabajo.


In breeding sheep high fertility rate is an important consideration factor. The association of genetic, nutritional and environmental conditions directly affects the fertility of ewes. There are high fertility sheep breeds (Texel, Suffolk) and other standard fertility breeds as (Romney, Criolla Araucana). Animal reproduction is modulated by sex hormones that act by binding to specific receptors. In sheep, alpha (ER-a) estrogen receptor is widely distributed in the reproductive system, modulating several mechanisms associated with reproductive system function. One factor possibly related to the difference in fertility between sheep breeds, is the differential expression level of these receptors in the reproductive system. In the present study a quantitative comparison of the immunohistochemical expression of ER-a was carried out in prepubertal sheep endometrium in high fertility (Texel) breed versus standard fertility (Araucana) breed, by measuring the integrated optical density in specific areas of the endometrium. Results indicate a significant difference between ER-a expression in endometrium off Texel breed ewes and Araucana breed ewes, and registered higher levels in all areas of evaluated Texel breed prepubertal ewes. This differential expression suggests a possible link between ER-a expression intensity and fertility in the breeds studied in this work.


Subject(s)
Animals , Female , Sheep , Estrogen Receptor alpha/metabolism , Endometrium/metabolism , Immunohistochemistry , Fertility
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