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1.
Endocrinology ; 153(6): 2701-13, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22508516

RESUMO

Aromatase is essential for estrogen production and is the target of aromatase inhibitors, the most effective endocrine treatment for postmenopausal breast cancer. Peripheral tissues in women, including the breast, express aromatase via alternative promoters. Female mice lack the promoters that drive aromatase expression in peripheral tissues; thus, we generated a transgenic humanized aromatase (Arom(hum)) mouse line containing a single copy of the human aromatase gene to study the link between aromatase expression in mammary adipose tissue and breast pathology. Arom(hum) mice expressed human aromatase, driven by the proximal human promoters II and I.3 and the distal promoter I.4, in breast adipose fibroblasts and myoepithelial cells. Estrogen levels in the breast tissue of Arom(hum) mice were higher than in wild-type mice, whereas circulating levels were similar. Arom(hum) mice exhibited accelerated mammary duct elongation at puberty and an increased incidence of lobuloalveolar breast hyperplasia associated with increased signal transducer and activator of transcription-5 phosphorylation at 24 and 64 wk. Hyperplastic epithelial cells showed remarkably increased proliferative activity. Thus, we demonstrated that the human aromatase gene can be expressed via its native promoters in a wide variety of mouse tissues and in a distribution pattern nearly identical to that of humans. Locally increased tissue levels, but not circulating levels, of estrogen appeared to exert hyperplastic effects on the mammary gland. This novel mouse model will be valuable for developing tissue-specific aromatase inhibition strategies.


Assuntos
Aromatase/genética , Perfilação da Expressão Gênica , Regulação Enzimológica da Expressão Gênica , Glândulas Mamárias Animais/metabolismo , Animais , Aromatase/metabolismo , Western Blotting , Estrogênios/metabolismo , Feminino , Humanos , Hiperplasia , Imuno-Histoquímica , Glândulas Mamárias Animais/enzimologia , Glândulas Mamárias Animais/patologia , Camundongos , Camundongos Transgênicos , Ovário/enzimologia , Ovário/metabolismo , Fosforilação , Regiões Promotoras Genéticas/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fator de Transcrição STAT5/metabolismo , Fatores de Tempo
2.
Mol Cell Endocrinol ; 355(1): 114-20, 2012 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-22342815

RESUMO

Adulthood weight gain predicts estrogen receptor-positive breast cancer. Because local estrogen excess in the breast likely contributes to cancer development, and aromatase is the key enzyme in estrogen biosynthesis, we investigated the role of local aromatase expression in weight gain-associated breast cancer risk in a humanized aromatase (Arom(hum)) mouse model containing the coding region and the 5'-regulatory region of the human aromatase gene. Compared with littermates on normal chow, female Arom(hum) mice on a high fat diet gained more weight, and had a larger mammary gland mass with elevated total human aromatase mRNA levels via promoters I.4 and II associated with increased levels of their regulators TNFα and C/EBPß. There was no difference in total human aromatase mRNA levels in gonadal white adipose tissue. Our data suggest that diet-induced weight gain preferentially stimulates local aromatase expression in the breast, which may lead to local estrogen excess and breast cancer risk.


Assuntos
Aromatase/genética , Neoplasias da Mama , Dieta Hiperlipídica/efeitos adversos , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Glândulas Mamárias Animais/enzimologia , Aumento de Peso/efeitos dos fármacos , Tecido Adiposo/metabolismo , Animais , Aromatase/metabolismo , Neoplasias da Mama/enzimologia , Neoplasias da Mama/genética , Proteína beta Intensificadora de Ligação a CCAAT/biossíntese , Modelos Animais de Doenças , Estrogênios/biossíntese , Feminino , Gônadas/metabolismo , Humanos , Glândulas Mamárias Animais/patologia , Glândulas Mamárias Humanas/enzimologia , Glândulas Mamárias Humanas/patologia , Camundongos , Regiões Promotoras Genéticas , RNA Mensageiro/análise , RNA Mensageiro/biossíntese , Fatores de Risco , Fator de Necrose Tumoral alfa/biossíntese
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