1.Sister chromatid exchange induced by diethylstilbestrol in lymphocytes from pregnant, premenopausal & postmenopausal women.
Hyun Ju BANG ; Hyun Mi PARK ; Young Deug CHOI ; Heung Gon KIM ; Ki Suk KIM
Korean Journal of Obstetrics and Gynecology 1992;35(7):1018-1024
No abstract available.
Diethylstilbestrol*
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Female
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Humans
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Lymphocytes*
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Siblings*
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Sister Chromatid Exchange*
2.A Case of Congenital Leukemia Cutis.
Young Suck RO ; Deug Gon MOON ; Chang Woo LEE ; Haeng Gon HAN ; Hahng LEE ; Jae Kyung CHOI
Korean Journal of Dermatology 2000;38(8):1089-1093
Congenital leukemia is a rare disease developing within the first 4 to 6 weeks of life, whose natural history is quite different from that of childhood and adult leukemia. Leukemia cutis occurs in 25% to 30% of infants with congenital leukemia and is more frequently associated with acute myeloid leukemia than acute lymphocytic leukemia. We report a case of congenital leukemia cutis in which a walnut-sized, slightly erythematous, dome-shaped tumor that had developed at left frontal area since birth was confirmed by skin biopsy. A review and analysis of Korean literature pertaining specially to leukemia cutis in congenital leukemia is presented along with the report of an additional case.
Adult
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Biopsy
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Humans
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Infant
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Leukemia*
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Leukemia, Myeloid, Acute
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Natural History
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Parturition
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Precursor Cell Lymphoblastic Leukemia-Lymphoma
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Rare Diseases
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Skin
3.En Plaque Meningioma in Thoracic Spine: Case Report.
Hyeon Seon PARK ; Sang Ho LEE ; Young Geun CHOI ; Sang Yeun LEE ; Ho Yeong KANG ; Deug Hee YOON ; Byung June JO
Journal of the Korean Radiological Society 2005;52(6):375-377
Spinal en plaque meningioma is rarely found in the spinal canal, although lateral sphenoid wing meningioma displays a propensity for growth en plaque. We encountered a case of completely circumferential spinal en plaque meningioma, which is an even rarer condition. Herein, we report the CT & MRI findings along with a review of the related literature.
Magnetic Resonance Imaging
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Meningioma*
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Spinal Canal
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Spine*
4.Adenovirus-mediated p53 tumor suppressor gene therapy against subcutaneous HuH7 hepatoma cell line nodule of nude mice.
Jong Young CHOI ; Young Min PARK ; Byun Hun BYUN ; Boo Sung KIM ; Eun Gyeong HONG ; Deug Yong SHIN ; Young Rim SEONG ; Dong Soo IM
Journal of Korean Medical Science 1999;14(3):271-276
Mutations of the tumor-suppressor gene p53 have been found in 30-50% cases of hepatocellular carcinoma (HCC). In this study, E1-negative adenoviral vector encoding wild-type p53 under the control of the human cytomegalovirus promoter (AdCMV-p53w) was constructed to evaluate its therapeutic efficacy against tumor nodules developing after injection of HuH7 cell lines in ten nude mice. When each nodule had reached 10 mm in perpendicular diameter, 1.5 x 10(8) pfu of AdCMV-p53w per session was injected intratumorally as follows: In group I (n=3), five sessions were injected every other day. In group II (n=3), only one session. Group III (n=4) as negative controls. The mice were sacrificed at 28 days post AdCMV-p53w injection. Tumor growth was significantly suppressed and delayed in group I and II compared to group III as compared by tumor volume at the end of observation. These results suggest that AdCMV-p53w may not only be effective in treating HCCs expressing mutant p53, but also useful as a local injectable gene therapy.
Adenoviruses, Human*
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Animal
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Apoptosis
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Carcinoma, Hepatocellular/therapy*
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Carcinoma, Hepatocellular/pathology
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Gene Therapy/methods*
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Genetic Vectors*
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Human
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Liver Neoplasms/therapy*
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Liver Neoplasms/pathology
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Mice
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Mice, Nude
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Neoplasm Transplantation
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Protein p53/genetics*
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Tumor Cells, Cultured
5.The Study on the Mechanism Regulating the Production of Extracellular Matrix in Renal Tubular Epithelial Cells Cultured in High Glucose Concentration.
Jae Ha HWANG ; Tae Hyun YOO ; Hyun Yong SONG ; Joo Seong KIM ; Young Su SONG ; Deug Lim CHONG ; Kyung Sup KIM ; Shin Wook KANG ; Ho Yung LEE ; Dae Suk HAN ; Kyu Hun CHOI
Korean Journal of Nephrology 2000;19(1):31-39
Thickening of tubular basement membrane and progressive tubulointerstitial fibrosis has been reported as important components of diabetic nephropathy, In order to investigate the mechanisms of tubulinterstitial changes in diabetic nephropathy, we evaluated the effects of a high concentration of glucose(25mM; 450mg/dL) on glucose transporter GLUT1 level, fibronectin production and tissue inhibitors of metalloproteinases (TIMP)-1 concentration in renal tubular(LLC-PK1) cells. As the effect of high glucose-induced alteration in LLC-PK1 cells, the expression of facilitative glueose transporter, GLUT1 was decreased after longer than 24-hours exposure to 25mM glucose, compared to control(5.6mM). The administration of protein kinase C (PKC) inhibitor GF109203X(10 microM) did not show significant effect on high glucose-induced decrease of GLUT1 level. On western blot analysis of fibronectin production, The exposure of LLC-PK cells to 25mM glucose for 48 hours significantly increasc4 fibro- nectin production, dose-dependently. The addition of GF102903X at the concentration of 10pM induced the significant increase of fibronectin level in LLC-PK1cells under glucose-free condition, whereas there was no significant effect on the high glucose-induced increase of fibronectin production. The addition of anti-TGF-beta antibody at 30 microgram/mL partly inhibited the high glucose-induced increase of fibronectin production. Concerning the changes of tissue inhibitor of metallo-proteinase(TIMP)-1 levels in the presence of high glucose, the exposure to high glucose for 24 and 43 hours increased TIMP-1 levels in culture supernatant of LLC-PK1 cells, dose-dependently. The TIMP-1 levels of 48-hour exposure to 15 and 25mM glucose were also significantly higher than those of 24-hourexposure. The treatment with 10 microM GF102903X or 30 microgram/mL anti-TGF-Beta antibody had no significant effects on TIMP-1 levels measured under the high glucose culture condition. In conclusion, the expression of facilitative glucose transporter, GLUT1 is inhibited and the production of fibronectin is increased in renal tubular cells cultured in the presence of high concentration of glucose, which is partly mediated by TGF-beta. The TIMP-1 level is also increased under high glucose culture condition. The enhanced productions of fibronectin and TIMP-1 of renal tubular cells under high glucose concentration may contribute to tubulointerstitial fibrosis that occurs in diabetic nephropathy.
Animals
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Basement Membrane
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Blotting, Western
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Diabetic Nephropathies
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Epithelial Cells*
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Extracellular Matrix*
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Fibronectins
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Fibrosis
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Glucose Transport Proteins, Facilitative
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Glucose*
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LLC-PK1 Cells
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Metalloproteases
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Protein Kinase C
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Swine
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Tissue Inhibitor of Metalloproteinase-1
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Transforming Growth Factor beta