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Cancer Res ; 62(22): 6385-9, 2002 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-12438220

RESUMO

The Sonic hedgehog (Shh) signaling pathway plays a critical role in normal cerebellar development and has been implicated in medulloblastomas, common malignant childhood tumors of the cerebellum. To test whether Shh mis-expression is sufficient for medulloblastoma formation, we used ultrasound biomicroscopy-guided in utero injection of a Shh-expressing retrovirus into the cerebellum of 13.5-day mouse embryos to show that direct activation of the Shh pathway can lead to tumor formation. Significantly, medulloblastomas were observed in 76% of the mice infected with Shh-expressing retrovirus. Furthermore, contrary to recent suggestions that the Shh transcriptional target Gli1 plays a critical role in Shh-induced tumorigenesis, we found that medulloblastomas form in Gli1 null mutant mice. We have developed an efficient mouse model of medulloblastoma and shown that Gli1 is not required for tumorigenesis when Shh signaling is activated upstream in the pathway.


Assuntos
Neoplasias Cerebelares/etiologia , Meduloblastoma/etiologia , Proteínas Oncogênicas/genética , Transativadores/fisiologia , Fatores de Transcrição/genética , Animais , Neoplasias Cerebelares/genética , Cerebelo/embriologia , Cerebelo/metabolismo , Feminino , Proteínas Hedgehog , Masculino , Meduloblastoma/genética , Camundongos , Camundongos Mutantes , Gravidez , Retroviridae/genética , Transdução de Sinais/fisiologia , Transativadores/biossíntese , Transativadores/genética , Proteína GLI1 em Dedos de Zinco
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