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1.
Oncogene ; 36(26): 3796, 2017 06 29.
Article in English | MEDLINE | ID: mdl-28218901

ABSTRACT

This corrects the article DOI: 10.1038/onc.2011.466.

2.
Cancer Gene Ther ; 19(11): 796-801, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23018623

ABSTRACT

In our previous works, we demonstrated that human neural stem cells (NSCs) transduced with the cytosine deaminase (CD) gene showed remarkable 'bystander killer effect' on glioma and medulloblastoma cells after administration of the prodrug 5-fluorocytosine (5-FC). In addition, herpes simplex virus thymidine kinase (TK) is a widely studied enzyme used for suicide gene strategies, for which the prodrug is ganciclovir (GCV). To apply this strategy to brain metastasis treatment, we established here a human NSC line (F3.CD-TK) expressing the dual suicide genes CD and TK. We examined whether F3.CD-TK cells intensified the antitumor effect on lung cancer brain metastases. In vitro studies showed that F3.CD-TK cells exerted a marked bystander effect on human lung cancer cells after treatment with 5-FC and GCV. In a novel experimental brain metastases model, intravenously administered F3 cells migrated near lung cancer metastatic lesions, which were induced by the injection of lung cancer cells via the intracarotid artery. More importantly, F3.CD-TK cells in the presence of prodrugs 5-FC and GCV decreased tumor size and considerably prolonged animal survival. The results of the present study indicate that the dual suicide gene-engineered, NSC-based treatment strategy might offer a new promising therapeutic modality for brain metastases.


Subject(s)
Brain Neoplasms/secondary , Gene Transfer Techniques , Genes, Transgenic, Suicide , Lung Neoplasms/pathology , Neural Stem Cells/metabolism , Administration, Intravenous , Animals , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/pharmacology , Brain Neoplasms/therapy , Bystander Effect , Carotid Arteries/metabolism , Cell Movement , Cell Survival , Cytosine Deaminase/genetics , Cytosine Deaminase/metabolism , Flucytosine/administration & dosage , Flucytosine/pharmacology , Ganciclovir/administration & dosage , Ganciclovir/pharmacology , Genetic Engineering/methods , Green Fluorescent Proteins/metabolism , HEK293 Cells , Humans , Kaplan-Meier Estimate , Mice , Mice, Nude , Neoplasms, Experimental/therapy , Prodrugs/administration & dosage , Prodrugs/pharmacology , Simplexvirus/enzymology , Simplexvirus/genetics , Thymidine Kinase/genetics , Thymidine Kinase/metabolism
3.
Oncogene ; 31(22): 2715-24, 2012 May 31.
Article in English | MEDLINE | ID: mdl-22020337

ABSTRACT

Glioblastomas (GBMs) are the most common and aggressive type of brain tumor. GBMs usually show hyperactivation of the PI3K-Akt pathway, a pro-tumorigenic signaling cascade that contributes to pathogenesis. Girdin, an actin-binding protein identified as a novel substrate of Akt, regulates the sprouting of axons and the migration of neural progenitor cells during early postnatal-stage neurogenesis in the hippocampus. Here, we show that Girdin is highly expressed in human glioblastoma (GBM). Stable Girdin knockdown in isolated GBM stem cells resulted in decreased expression of stem cell markers, including CD133, induced multilineage neural differentiation, and inhibited in vitro cell motility, ex vivo invasion, sphere-forming capacity and in vivo tumor formation. Furthermore, exogenous expression of the Akt-binding domain of Girdin, which competitively inhibits its Akt-mediated phosphorylation, diminished the expression of stem cell markers, SOX2 and nestin, and migration on the brain slice and induced the expression of neural differentiation markers glial fibrillary acidic protein/ßIII Tubulin. Our results reveal that Girdin is required for GBM-initiating stem cells to sustain the stemness and invasive properties.


Subject(s)
Brain Neoplasms/pathology , Cell Differentiation , Cell Movement , Glioblastoma/pathology , Microfilament Proteins/metabolism , Neoplastic Stem Cells/metabolism , Neoplastic Stem Cells/pathology , Vesicular Transport Proteins/metabolism , AC133 Antigen , Animals , Antigens, CD/genetics , Antigens, CD/metabolism , Biomarkers/metabolism , Blotting, Western , Brain Neoplasms/genetics , Brain Neoplasms/metabolism , Cell Proliferation , Female , Gene Expression Regulation, Neoplastic , Glial Fibrillary Acidic Protein/genetics , Glial Fibrillary Acidic Protein/metabolism , Glioblastoma/genetics , Glioblastoma/metabolism , Glycoproteins/genetics , Glycoproteins/metabolism , Humans , Immunoenzyme Techniques , Immunoprecipitation , Intermediate Filament Proteins/genetics , Intermediate Filament Proteins/metabolism , Mice , Mice, Inbred BALB C , Mice, Inbred NOD , Mice, Nude , Mice, SCID , Microfilament Proteins/antagonists & inhibitors , Microfilament Proteins/genetics , Neoplasm Grading , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Nestin , Peptides/genetics , Peptides/metabolism , Phosphorylation , Proto-Oncogene Proteins c-akt/genetics , Proto-Oncogene Proteins c-akt/metabolism , RNA, Messenger/genetics , RNA, Small Interfering/genetics , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction , Tumor Cells, Cultured , Vesicular Transport Proteins/antagonists & inhibitors , Vesicular Transport Proteins/genetics
5.
J Pediatr Surg ; 36(4): 622-5, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11283891

ABSTRACT

A congenital absence of the portal vein (CAPV) is a rare malformation, which almost is always associated with other anomalies such as hepatic tumors and cardiac malformations. This case report describes a 3-year-old girl with a congenital absence of the portal vein, focal nodular hyperplasia (FNH) of the liver, and a congenital choledochal cyst (CCC). Angiography findings showed the mesenteric vein and splenic vein to be joined together to form a common trunk that entered the inferior vena cava directly above the liver. This is the first known reported case of CAPV with concurrent CCC. J Pediatr Surg 36:622-625.


Subject(s)
Abnormalities, Multiple/diagnosis , Choledochal Cyst/diagnosis , Focal Nodular Hyperplasia/diagnosis , Focal Nodular Hyperplasia/surgery , Portal Vein/abnormalities , Angiography , Biopsy, Needle , Child, Preschool , Female , Follow-Up Studies , Humans , Liver/pathology , Portal Vein/embryology , Tomography, X-Ray Computed , Treatment Outcome
6.
Brain Tumor Pathol ; 18(2): 155-9, 2001.
Article in English | MEDLINE | ID: mdl-11908873

ABSTRACT

A 74-year-old man manifested disturbed consciousness and right hemiparesis. Computed tomography revealed a left frontal parasagittal meningeal tumor with extensive peritumoral brain edema and skull invasion. Subtotal removal was performed. Five years later, he underwent two more operations of massive recurrences. Pathological studies revealed anaplastic meningioma with two different histological areas. One was an epithelial and meningothelial area, and the other was a papillary and rhabdoid area. In the papillary and rhabdoid area, small tumor cells with a high nucleus/cytoplasm ratio proliferated densely around the dilated central capillaries with a pseudopapillary pattern. Many rhabdoid cells (vimentin ++, cytokeratin AE1/AE3 +, epithelial membrane antigen [EMA] + +) tended to be distributed far from the central capillaries. There were many mitotic figures near the central vessels. Dense MIB1-positive nuclei were also observed near the central vessels. The trabecular pattern of the tumor cells in the epithelial area was quite different from the histological features of chordoid meningioma.


Subject(s)
Meningeal Neoplasms/pathology , Meningioma/pathology , Aged , Biomarkers, Tumor/analysis , Cell Differentiation , Humans , Keratins/analysis , Magnetic Resonance Imaging , Male , Meningeal Neoplasms/chemistry , Meningioma/chemistry , Neoplasm Proteins/analysis , Neoplasm Recurrence, Local , Neoplastic Stem Cells/chemistry , Neoplastic Stem Cells/ultrastructure , Nerve Tissue Proteins/analysis , Vimentin/analysis
7.
Electromyogr Clin Neurophysiol ; 34(7): 409-14, 1994.
Article in English | MEDLINE | ID: mdl-7859669

ABSTRACT

We examined the relationship between the Na and Pa components of human MLRs and the performance of different tasks. We also investigated whether MLRs are reliable indices of activity in the central motor-sensory system. The click stimuli we used consistently evoked the Na and Pa components. At CZ, the Na and Pa components significantly decreased for all tasks other than pegging with right hand while at FZ, these components were significantly decreased for all tasks. The Na and Pa latencies were slightly increased during task performances. These results indicate that the Na and Pa components of human MLRs decreased when various tasks were performed, while subjects were concentrating. A general principle of evoked potentials is that latencies decrease as amplitudes increase in excitation due to neural activation. Thus, it would appear that, under the conditions of this study, the pathways from the reticular formation and the thalamus to the primary auditory cortex were inhibited. Since the thalamus is considered to be the relay region for poly-sensory inputs, it is thought that the attenuation of the MLRs and SEPs occurs at the level of cerebral cortex, including the reticular formation, the thalamus, and the primary auditory cortex. Accordingly, since it is inferred that central factors are responsible for the attenuation of the MLRs, Na and Pa components observed during the performance of tasks carried out in the present experiment, it may be concluded that MLRs are reliable indices of activity in the central-motor system.


Subject(s)
Evoked Potentials, Auditory/physiology , Reaction Time/physiology , Acoustic Stimulation , Adolescent , Adult , Electroencephalography , Female , Humans , Male , Reference Values , Task Performance and Analysis
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