Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Type of study
Language
Publication year range
1.
Transpl Infect Dis ; 17(6): 886-9, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26426525

ABSTRACT

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.


Subject(s)
Antiprotozoal Agents/therapeutic use , Bone Marrow Transplantation/adverse effects , Dysentery, Amebic/drug therapy , Graft vs Host Disease/complications , Metronidazole/therapeutic use , Dysentery, Amebic/etiology , Humans , Immunocompromised Host , Male , Middle Aged
2.
Cancer Gene Ther ; 13(4): 385-92, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16244591

ABSTRACT

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.


Subject(s)
Angiogenic Proteins/biosynthesis , Brain Neoplasms/blood supply , Glioblastoma/blood supply , Neovascularization, Pathologic/therapy , Adenoviridae/genetics , Angiogenic Proteins/genetics , Animals , Brain Neoplasms/pathology , Brain Neoplasms/therapy , Cell Line, Tumor , Genetic Therapy , Genetic Vectors , Glioblastoma/pathology , Glioblastoma/therapy , Humans , Mice , Mice, SCID , Neoplasm Transplantation , RNA, Messenger/metabolism , Receptors, G-Protein-Coupled , Transduction, Genetic
SELECTION OF CITATIONS
SEARCH DETAIL
...