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1.
Transpl Infect Dis ; 17(6): 886-9, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26426525

RESUMO

Amoebiasis has rarely been reported in patients undergoing hematopoietic stem cell transplantation, although it is a world-wide infection and extremely common. We present a case of intestinal amoebiasis unexpectedly revealed by colonoscopy after allogeneic bone marrow transplantation from a human leukocyte antigen-mismatched unrelated donor for acute myeloid leukemia arising from chronic myelomonocytic leukemia and successfully treated by metronidazole.


Assuntos
Antiprotozoários/uso terapêutico , Transplante de Medula Óssea/efeitos adversos , Disenteria Amebiana/tratamento farmacológico , Doença Enxerto-Hospedeiro/complicações , Metronidazol/uso terapêutico , Disenteria Amebiana/etiologia , Humanos , Hospedeiro Imunocomprometido , Masculino , Pessoa de Meia-Idade
2.
Cancer Gene Ther ; 13(4): 385-92, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16244591

RESUMO

Glioblastomas are the most common primary brain tumors in adults. These tumors exhibit a high degree of vascularization, and malignant progression from astrocytoma to glioblastoma is often accompanied by increased angiogenesis and the upregulation of vascular endothelial growth factor and its receptors. In this study, we investigated the in vivo antiangiogenic and antitumor effects of brain-specific angiogenesis inhibitor 1 (BAI1) using human glioblastoma cell lines. Glioblastoma cells were transduced with an adenoviral vector encoding BAI1 (AdBAI1), and Northern and Western blot analyses, respectively, demonstrated BAI1 mRNA and protein expression in the transduced tumor cells. Using an in vivo neovascularization assay, we found that angiogenesis surrounding AdBAI1-transduced glioblastoma cells transplanted into transparent skinfold chambers of SCID mice was significantly impaired compared to control treated cells. Additionally, in vivo inoculation with AdBAI1 of established subcutaneous or intracerebral transplanted tumors significantly impaired tumor growth and promoted increased mouse survival. Morphologically, the tumors exhibited signs of impaired angiogenesis, such as extensive necrosis and reduced intratumoral vascular density. Taken together, these data strongly indicate that BAI1 may be an excellent gene therapy candidate for the treatment of brain tumors, especially human glioblastomas.


Assuntos
Proteínas Angiogênicas/biossíntese , Neoplasias Encefálicas/irrigação sanguínea , Glioblastoma/irrigação sanguínea , Neovascularização Patológica/terapia , Adenoviridae/genética , Proteínas Angiogênicas/genética , Animais , Neoplasias Encefálicas/patologia , Neoplasias Encefálicas/terapia , Linhagem Celular Tumoral , Terapia Genética , Vetores Genéticos , Glioblastoma/patologia , Glioblastoma/terapia , Humanos , Camundongos , Camundongos SCID , Transplante de Neoplasias , RNA Mensageiro/metabolismo , Receptores Acoplados a Proteínas G , Transdução Genética
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