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1.
Medicina (B.Aires) ; 57(Supl.2): 55-69, Aug. 1997.
Artigo em Espanhol | LILACS | ID: lil-320009

RESUMO

We have developed an experimental model in which the administration of progestins induces mammary tumors in female virgin BALB/c mice. In this paper we review the morphological and biological features of progestin-induced tumors, such as estrogen receptor (ER) and progesterone receptor (PR) patterns of expression, hormone dependence and epidermal growth factor receptors (EGF-R) we also examine our data concerning the systemic effects of medroxyprogesterone acetate (MPA) as regards its stimulating EGF synthesis in salivary glands and its subsequent increase in serum. This growth factor seems to play an important role in the induction of mammary tumors. Direct MPA proliferative effects mediated by PR were demonstrated using primary cultures of progestin-dependent (PD) mammary tumors. Antiprogestins inhibited cell growth beyond control values, suggesting that PR are involved in cell proliferation even in the absence of the ligand. Progesterone-independent (PI) tumors expressing high levels of PR and ER are also inhibited by estrogen or antiprogestin treatment, suggesting that PR are involved in the control of autonomous tumor growth. Estrogen-resistant variants may be selected which may revert to an estrogen-sensitive phenotype after several transplants in untreated mice. The similarities between the tumors obtained with this model and human breast cancer as regards morphological features, evolution and the regulation of growth control converts this model into a useful tool to explore the mechanisms related with acquisition of hormone independence and autonomous tumor growth.


Assuntos
Humanos , Animais , Feminino , Criança , Camundongos , Adenocarcinoma , Neoplasias Hormônio-Dependentes/patologia , Neoplasias Mamárias Experimentais/patologia , Receptores ErbB/análise , Receptores de Estrogênio/análise , Receptores de Progesterona , Adenocarcinoma , Progressão da Doença , Neoplasias Pulmonares , Acetato de Medroxiprogesterona , Camundongos Endogâmicos BALB C , Neoplasias Mamárias Experimentais/induzido quimicamente
2.
Bol. Acad. Nac. Med. B.Aires ; 69(2): 483-92, jul.-dic. 1991. ilus
Artigo em Espanhol | LILACS | ID: lil-157615

RESUMO

En nuestro modelo experimental el acetato de medroxiprogesterona induce adenocarcinomas de mama en hembras vírgenes de la cepa BALB/c. Estos tumores, con receptores para progesterona y estrógenos, originaron líneas de crecimiento hormono-dependientes (HD) o independiente (HI)..La progesterona y el MPA estímulan el crecimiento de las HD y los estrógenos inhiben el crecimiento de las HD y HI. En este trabajo demostramos que cultivos primarios de tumores HD conservan la misma sensibilidad hormonal que los tumores parenterales: la proliferación celular aumenta con concentraciones de MPA 10-9-10-7 M y es inhibida con estrógenos 10-9 o 10-7 M aun en presencia de MPA. Estos resultados sugerirían que las hormonas actúan directamente sobre las células tumorales. En experimentos "in vivo" demostraron que animales tratados con progesterona también desarrollaron adenocarcinomas de mama aunque la incidencia fue menor que en los tratados con MPA. Curiosamente se observó que la mayoría de los adenocarcinomas de mama inducidos por progesterona eran lobulillares y III mientras que en los tratados con MPA la mayoría fue ductal y HD. También se demostró que la ovariectomía y la sialoadenectomía disminuyen el poder carcinogénico del MPA sin alterar el patrón morfológico: 70 por ciento ductal y HD


Assuntos
Animais , Ratos , Adenocarcinoma/induzido quimicamente , Neoplasias Mamárias Experimentais/induzido quimicamente , Medroxiprogesterona/efeitos adversos , Progesterona/efeitos adversos , Receptores da Somatotropina , Estrogênios , Ovariectomia
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