Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros

Base de dados
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Nat Med ; 8(9): 995-1003, 2002 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-12185361

RESUMO

Angiogenesis is a highly regulated process that results from the sequential actions of naturally occurring stimulators and inhibitors. Here, we show that parathyroid hormone-related peptide, a peptide hormone derived from normal and tumor cells that regulates bone metabolism and vascular tone, is a naturally occurring angiogenesis inhibitor. Parathyroid hormone-related peptide or a ten-amino-acid peptide from its N terminus inhibits endothelial cell migration in vitro and angiogenesis in vivo by activating endothelial cell protein kinase A. Activation of protein kinase A inhibits cell migration and angiogenesis by inhibiting the small GTPase Rac. In contrast, inhibition of protein kinase A reverses the anti-migratory and anti-angiogenic properties of parathyroid hormone-related peptide. These studies show that parathyroid hormone-related peptide is a naturally occurring angiogenesis inhibitor that functions by activation of protein kinase A.


Assuntos
Inibidores da Angiogênese/metabolismo , Inibidores da Angiogênese/farmacologia , Proteínas Quinases Dependentes de AMP Cíclico/metabolismo , Proteínas/metabolismo , Proteínas/farmacologia , Sulfonamidas , Animais , Testes de Carcinogenicidade , Movimento Celular , Embrião de Galinha , Proteínas Quinases Dependentes de AMP Cíclico/antagonistas & inibidores , Endotélio Vascular , Inibidores Enzimáticos/farmacologia , Fator 2 de Crescimento de Fibroblastos/farmacologia , Técnicas de Transferência de Genes , Isoquinolinas/farmacologia , Camundongos , Neovascularização Patológica/tratamento farmacológico , Neovascularização Fisiológica/efeitos dos fármacos , Proteína Relacionada ao Hormônio Paratireóideo , Mapeamento de Peptídeos , Proteínas/genética , Proteínas rac de Ligação ao GTP/metabolismo
2.
Clin Cancer Res ; 12(8): 2602-6, 2006 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-16638872

RESUMO

PURPOSE: Metastatic bone disease is one of the major causes of morbidity and mortality in prostate cancer patients. Bisphosphonates are currently used to inhibit bone resorption and reduce tumor-induced skeletal complications. More effective bisphosphonates would enhance their clinical value. EXPERIMENTAL DESIGN: We tested several bisphosphonates in a green fluorescent protein (GFP)-expressing human prostate cancer nude mouse model. The in vivo effects of four bisphosphonates, including pamidronate, etidronic acid, and olpadronate, on bone tumor burden in mice intratibially inoculated with PC-3-GFP human prostate cancer cells were visualized by whole-body fluorescence imaging and X-ray. RESULTS: The PC-3-GFP cells produced extensive bone lesions when injected into the tibia of immunocompromised mice. The skeletal progression of the PC-3-GFP cell growth was monitored by GFP fluorescence and the bone destruction was evaluated by X-ray. We showed that 3,3-dimethylaminopropane-1-hydroxy-1,1-diphosphonic acid (olpadronate) was the most effective bisphosphonate treatment in reducing tumor burden as assessed by GFP imaging and radiography. The GFP tumor area and X-ray score significantly correlated. Reduced tumor growth in the bone was accompanied by reduced serum calcium, parathyroid hormone-related protein, and osteoprotegerin. CONCLUSIONS: The serum calcium, parathyroid hormone-related protein, and osteoprotegerin levels were significantly correlated with GFP area and X-ray scores. Treatment with olpadronate reduced tumor growth in the bone measured by GFP and X-ray imaging procedures. Imaging of GFP expression enables monitoring of tumor growth in the bone and the GFP results complement the X-ray assessment of bone disease. The data in this report suggest that olpadronate has potential as an effective inhibitor of the skeletal progression of clinical prostate cancer.


Assuntos
Neoplasias Ósseas/prevenção & controle , Difosfonatos/uso terapêutico , Proteínas de Fluorescência Verde/metabolismo , Neoplasias da Próstata/tratamento farmacológico , Ensaios Antitumorais Modelo de Xenoenxerto/métodos , Animais , Conservadores da Densidade Óssea/uso terapêutico , Neoplasias Ósseas/metabolismo , Neoplasias Ósseas/secundário , Cálcio/sangue , Linhagem Celular Tumoral , Progressão da Doença , Glicoproteínas/sangue , Proteínas de Fluorescência Verde/genética , Humanos , Masculino , Camundongos , Camundongos Nus , Osteoprotegerina , Pamidronato , Proteína Relacionada ao Hormônio Paratireóideo/sangue , Neoplasias da Próstata/metabolismo , Neoplasias da Próstata/patologia , Receptores Citoplasmáticos e Nucleares/sangue , Receptores do Fator de Necrose Tumoral/sangue , Fatores de Tempo , Resultado do Tratamento
3.
Endocr Pract ; 11(3): 184-9, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16239205

RESUMO

OBJECTIVE: To describe a case of metastatic rhabdomyosarcoma originating from the sphenoid sinus in a patient previously treated with conventional irradiation for a prolactinoma, presenting as hypercalcemia in the setting of a normal level of serum parathyroid hormone-related protein (PTHrP). METHODS: We report the case of a patient who underwent remote pituitary irradiation for a prolactinoma and then presented decades later with hypercalcemia of unknown cause. His clinical course, the initial biochemical and radiologic investigations, and the results of examination of pathology specimens are reviewed. RESULTS: The patient was found to have a mass in the sphenoid sinus. The pathologic features were consistent with alveolar rhabdomyosarcoma. Although he had a normal serum PTHrP level, staining of his tumor with an antibody against PTHrP revealed local production of PTHrP at the tumor margins. His bone marrow biopsy specimen showed 100% involvement with rhabdomyosarcoma. CONCLUSION: PTHrP staining of pathology specimens might explain hypercalcemia of undetermined cause in patients with a known malignant lesion, in whom elevated serum PTHrP levels cannot be demonstrated.


Assuntos
Neoplasias da Medula Óssea/metabolismo , Neoplasias da Medula Óssea/secundário , Neoplasias Encefálicas/metabolismo , Neoplasias Encefálicas/secundário , Hipercalcemia/etiologia , Proteína Relacionada ao Hormônio Paratireóideo/biossíntese , Neoplasias Hipofisárias/patologia , Neoplasias Hipofisárias/radioterapia , Rabdomiossarcoma/metabolismo , Rabdomiossarcoma/secundário , Seio Esfenoidal , Idoso , Difosfonatos/uso terapêutico , Evolução Fatal , Humanos , Hipercalcemia/tratamento farmacológico , Imidazóis/uso terapêutico , Técnicas Imunoenzimáticas , Imuno-Histoquímica , Masculino , Pamidronato , Ácido Zoledrônico
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA