1.ene Expression of Enzymes Related to Glutathione Metabolism in Anticancer Drug-resistant L1210 Sublines.
Seong Yong KIM ; Jae Ryong KIM ; Jung Hye KIM
Yeungnam University Journal of Medicine 1995;12(1):32-47
Glutathione(GSH) has a very important role in detoxification of cells and is closely related to antitumor drug-resistance of cancer cells. In order to evaluate the importance of glutathione metabolism in the drug-resistant cancer cells, the concentration of celluar GSH and activities of y-glutamylcysteine synthetase(GCS), y-glutamyl transpeptidase (GGT) and glutathione S-transferases(GST) in the adriamycin, vincristine, or cisplatin resistant L1210 (L1210AdR; L1210VcR, or L12100s) sublines were measured. Expression and amplification of GCS, GGT, and GST-i7 genes were also observed in the parent L1210 and the drug-resistant L1210 sublines. The concentration of GSH was increased 5.34 fold in L12100s, 2.83 fold in L1210VcR, and 1.78 fo-d in L1210AdR, compared to L1210. The activities of GCS and GGT were -increased in drug-resistant L1210 sublines. The GST activity was increased in L1210VcR and L1210Cis but decreased in L1210AdR compared to L1210. Expression of GCS, GGT, and GST-rr genes were increased in the resistant L1210 sublines compare to the parent L1210 in northern blot analyses. Overexpression of GCS, GGT, and GST-77 were observed in the resistant sublines, and the increases of the concentration of glutathione and the activities of GCS and GGT in the resistant sublines may be involved in a part of the drug-resistance in the resistant sublines.
Blotting, Northern
;
Cisplatin
;
Doxorubicin
;
Drug Resistance
;
Glutathione*
;
Humans
;
Metabolism*
;
Parents
;
Vincristine
2.Study for Metabolism of Resistant Production in Anticancer drug Resistant Stomach Cancer Cell SNU-1.
Jung Hye KIM ; Mi Wha KANG ; Jae Ryong KIM
Yeungnam University Journal of Medicine 1989;6(2):195-205
Development of drug resistance in tumors during treatment is a major factor limiting the clinical use of anticancer agents. When tumor cells acquire resistance to anticancer drug, they show cross-resistance to other antitumor agents. In the present study, SNU-1 cell was induced adriamycin 10-7 drug resistance, SNU-1/ADR, in vitro culture system. We got the doubling time and number for viability test during 96 hours by MTT assay. To investigate the cross resistance of various anticancer drugs in human stomach cancer cell SNU-1 and SNU-1/ADR, We compared IC50 (drug concentration of 50% reduction) and the relative resistance (RR). SNU-1/ADR was expressed multidrug resistant with vinblastine (RR;>31.62), vincristine (RR;29.50), dactinomycin (RR;21.37), epirubicin (RR;17.78), daunorubicin (RR;14.12), adriamycin (RR;7.76), and etoposide (RR;4.46), and other drugs, 5-fluorouracil, cisplatin, cyclophosphamide, methotrexate, and calarubicin, have not cross resistant with adriamycin. There was double minute chromosome in SNU-1/ADR by karyotyping although this change was not seen in SUN-1.
Antineoplastic Agents
;
Cisplatin
;
Cyclophosphamide
;
Dactinomycin
;
Daunorubicin
;
Doxorubicin
;
Drug Resistance
;
Epirubicin
;
Etoposide
;
Fluorouracil
;
Humans
;
In Vitro Techniques
;
Inhibitory Concentration 50
;
Karyotyping
;
Metabolism*
;
Methotrexate
;
Stomach Neoplasms*
;
Stomach*
;
Vinblastine
;
Vincristine
3.Production of Monoclonal Antibody to Polychlorinated Biphenyl Induced Cytochrome P-450 LMII in Rat Liver.
Jung Hye KIM ; Jae Ryong KIM ; Ki Yung LEE
Yeungnam University Journal of Medicine 1986;3(1):103-110
Cytochrome P-450 (CP-450) is one of the three components of the liver microsomal enzyme system which hydroxylates fatty acids, hydrocarbons and a variety of drugs and other foreign compounds. Female Balb/c mice were immunized with purified polychlorinated biphenyl (PCB) – induced CP-450 LMII. The spleen cells derived from immunized mice were fused with SP2 myeloma cells using polyethylene glycol (PEG 3500). The hybrid cells were selected by hypoxanthine-aminopterin-thymidine (HAT) medium and the culture fluid were screened by enzyme-linked immunosorbent assay to CP450 LMII. The hybrid cells(×107) were inoculated into intraperitoneal cavity of Balb/c mice for the purpose of production of ascetic fluids. Monoclonal antibody (Mab) was purified from ascitic fluid by DEAE cellulose ion exchange chromatography and I¹²⁵ labeled Mab was also confirmed by autoradiography and SDS-polyacrylamide gel electrophoresis (MW:55,000 and 110,000)
Animals
;
Ascitic Fluid
;
Autoradiography
;
Chromatography, Ion Exchange
;
Cytochrome P-450 Enzyme System*
;
Cytochromes*
;
DEAE-Cellulose
;
Electrophoresis
;
Enzyme-Linked Immunosorbent Assay
;
Fatty Acids
;
Female
;
Humans
;
Hybrid Cells
;
Hydrocarbons
;
Liver*
;
Mice
;
Polyethylene Glycols
;
Rats*
;
Spleen
4.Purification of Band 3 from the Human Erythrocyte Membrane and its Incorporation into Liposome.
Jae Ryong KIM ; Jung Hye KIM ; Ki Yung LEE
Yeungnam University Journal of Medicine 1986;3(1):41-48
Band 3, the predominant 95,000 dalton anion transport protein, is the major intrinsic glycoprotein of the human erythrocyte membrane. This anion carrier exists as a dimer and binds the cytoskeletons such as spectrin, ankyrin and actin. And the liposomes are vesicular structures which form spontaneously upon hydration of phospholipids. These artificial lipid vesicles have been investigated as model of the biological membranes and as a mean of improving the delivery of nucleic acids, drugs, proteins and biological substances to specific target tissues and cells. In this study, we were purified Band 3 from the human erythrocyte membrane (ghost) was prepared by hemolysis of intact human erythrocyte with weak alkali-hypotonic solution. Band 6 was removed from ghost by extracting with solution of an ionic strength of 0.15. Band 3 and Band 4 were solubilized selectively by extracting Band 6-depleted ghosts with Triton X-100 under nondenaturing conditions. Band 3 was then purified from Triton X-100 extract treated with p-chloromercuribenzoate by sucrose density gradient ultracentrifugation. This purified Band 3 was incorporated into liposomes prepared by reverse-phase evaporation. Phosphatidyl L-serine and cholesterol (1:1 molar ratio) were dissolved in chloroform and the chloroform was removed by rotator evaporation under reduced pressure. Band 3 solution without Triton X-100 was introduced into a mixture of lipids and diethylether. Diethylether was subsequently removed by evaporation. This purified Band 3 and its incorporation into liposomes were confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
Actins
;
Ankyrins
;
Chloroform
;
Cholesterol
;
Cytoskeleton
;
Electrophoresis
;
Erythrocyte Membrane*
;
Erythrocytes*
;
Glycoproteins
;
Hemolysis
;
Humans*
;
Liposomes*
;
Membranes
;
Molar
;
Nucleic Acids
;
Octoxynol
;
Osmolar Concentration
;
Phospholipids
;
Serine
;
Sodium
;
Spectrin
;
Sucrose
;
Ultracentrifugation
5.Clinical and Histopathological Observation on Acquired Melanocytic Nevus ( 1975 ~ 1985 ).
Jae Chul LEE ; Eun Jung CHYUNG ; See Ryong PARK
Korean Journal of Dermatology 1988;26(6):874-878
This clinical and histopatholgical study was performed with 149 cases of acquired melanocyticnevi, which were obtained as surgical specimens from 1975 to 1985 at Depa.rtment of Clinical Pathology, Seoul Red Cross Hopital. The results were as follows: 1) Histologic subdivision of melanocytic nevus into junctional(,J), IJC, compound (C,"), ICI, and intradermal(I) is used. IJC is a lesion in an intermediate state between ,junctional and compound nevus, and ICI, between compound and intradermal nevus. 2) The age distribution of the excisional melanocytic nevus peaks during the third decade of life, with 47% of patients between 21 40 year old of age. 3) Of l49 specimens with excisional melanocytic nevus, the number of junctional, IJC, compound, ICI and intradermal nevus were 17, 4, 21, 32 and 75 in each group And so, it is likely that evolution of the melanocytic nevus have an increased opportunity for surgical excision. 4) Among the 17 cases of junctional nevus, one case is found in 5th and the other one in 7th decade. 5) In distvibution of melanocytic nevus, head including face is the most common site among the body area and then trunk, neck, lower and upper extremity in decreasing orders.
Adult
;
Age Distribution
;
Head
;
Humans
;
Neck
;
Nevus
;
Nevus, Intradermal
;
Nevus, Pigmented*
;
Pathology, Clinical
;
Red Cross
;
Seoul
;
Upper Extremity
6.Mutagenicity of Human Urine Excreted after Ingestion of Roast Beef.
Dong Gu SHIN ; Jung Hee KIM ; Jae Ryong KIM
Yeungnam University Journal of Medicine 1987;4(2):105-111
This study was undertaken to observe the mutagenic occurrence in urine excreted after the ingestion of roast beef. Two healthy nonsmoker persons of both sex were selected for this test, employing two strains (TA98, TA100) of Salmonella typhimurium according to Ames' method. The mutagenic activity began to appear in urine of both sex three hours after ingestion of 300 g of roast beef, gradually increasing until 6 hours and declining thereafter.
Eating*
;
Humans*
;
Methods
;
Red Meat*
;
Salmonella typhimurium
7.The Change of Glutathione Metabolism in Liver and Kidney of Cisplatin treated Rats.
Seong Yong KIM ; Jae Yong CHUNG ; Jae Ryong KIM ; Jung Hye KIM
Yeungnam University Journal of Medicine 1994;11(2):262-269
Glutathione (GSH) is a well-known antioxidative cellular component which is ubiquitous in nature. Several enzymes involved in GSH metabolism and recycling have been found to play important roles in detoxification of xenobiotics and free radicals. In this study, total GSH content, activity of GSH peroxidase and GSH reductase were measured in liver and kidney of cisplatin treated rats. Total GSH content (mM/g protein) of liver was higher in cisplatin treated rats (1.51±0.28) than of nontreated control (0.95±0.28), and in kidney, it was also higher in cisplatin treated rats (0.87±0.20) than that of control (0.68±0.14). The activity of GSH peroxidase (µM/mg protein/min) was lower in liver of cisplatin treated rats (348.0±18.54) than that of control (415.5±53.15), in kidney it was increase din cisplatin treated rats (380.5±51.86) compared to control (327.3±20.36). The activity of GSH reductase (µM/mg protein/min) was higher in liver of cisplatin treated rats (3.09±0.88) than that of control (2.28±0.61), in kidney it was also higher in cisplatin treated rats (8.50±2.62) than that of control (3.30±1.10). In summary, detoxification of ciplatin was revealed lesser effect in kidney as show increasion of GSH peroxidase and reductase and detoxification of cisplatin was expressed effectively in liver by increasing of GSH content and decreasing GSH peroxidase.
Animals
;
Cisplatin*
;
Free Radicals
;
Glutathione*
;
Kidney*
;
Liver*
;
Metabolism*
;
Oxidoreductases
;
Peroxidase
;
Rats*
;
Recycling
;
Xenobiotics
8.An Experimental Study of Pathogenesis of Duodenal Ulceration Produced by Mepirizole.
Myung Jae KANG ; Jae Ryong JUNG ; Hye Soo LEE ; Sang Ho KIM
Korean Journal of Pathology 1988;22(4):383-392
To investigate the pathogenesis of the duodenal ulceration produced by mepirizole (1-(4-methoxy-6-methyl-2-pyrimidinyl)-3-methyl-5-methoxypyrazole) in rat, the effects of various concentraion and sorts of antiulcer drugs and truncal vagotomy on the mepirizole (200 mg/kg of body weight) induced duodenal ulcers were observed morphologically, and after mepirizole administration (200 mg/kg), amount and acidity of gastric jucie were measured sequently. The results were as follows: 1) In the control group of fasting for 24 hours after mepirizole administration only, duodenal ulcers were developed in all animals with 21.5+/-5.8 mm2 of ulcer index, perforation rate was 15%, and mortality rate was 0%. But lesions of the stomach were hemorrhagic and erosive with erosion index of 3.8+/-1.6 mm2. 2) The antiulcer drugs were significantly inhibited duodenal ulceration and gastric erosion produced by mepirizole although the inhibition effects were different. 3) After truncal vagotomy, duodenal ulcer and gastric erosion induced by mepirizole were also significantly inhibited. 4) On the gastric analysis, decrease of amount, increase of acidity, and decrease of concentration of gastric juice were observed after administration of mepirizole compared with nontreated normal group. Above findings suggest that the pathogenesis of the duodenal ulceration by mepirizole is the action of gastric acid on the duodenal mucosa with breakdown of defence mechanisms of the duodenum.
Animals
;
Mortality
9.Comparison of polymer-based temporary crown and fixed partial denture materials by diametral tensile strength.
Seung Ryong HA ; Jae Ho YANG ; Jai Bong LEE ; Jung Suk HAN ; Sung Hun KIM
The Journal of Advanced Prosthodontics 2010;2(1):14-17
PURPOSE: The purpose of this study was to investigate the diametral tensile strength of polymer-based temporary crown and fixed partial denture (FPD) materials, and the change of the diametral tensile strength with time. MATERIAL AND METHODS: One monomethacrylate-based temporary crown and FPD material (Trim) and three dimethacrylate-based ones (Protemp 3 Garant, Temphase, Luxtemp) were investigated. 20 specimens (the empty set 4 mm x 6 mm) were fabricated and randomly divided into two groups (Group I: Immediately, Group II: 1 hour) according to the measurement time after completion of mixing. Universal Testing Machine was used to load the specimens at a cross-head speed of 0.5 mm/min. The data were analyzed using one-way ANOVA, the multiple comparison Scheffe test and independent sample t test (alpha = 0.05). RESULTS: Trim showed severe permanent deformation without an obvious fracture during loading at both times. There were statistically significant differences among the dimethacrylate-based materials. The dimethacrylate-based materials presented an increase in strength from 5 minutes to 1 hour and were as follows: Protemp 3 Garant (23.16 - 37.6 MPa), Temphase (22.27 - 28.08 MPa), Luxatemp (14.46 - 20.59 MPa). Protemp 3 Garant showed the highest value. CONCLUSION: The dimethacrylate-based temporary materials tested were stronger in diametral tensile strength than the monomethacrylate-based one. The diametral tensile strength of the materials investigated increased with time.
Acrylic Resins
;
Bisphenol A-Glycidyl Methacrylate
;
Collodion
;
Composite Resins
;
Crowns
;
Denture, Partial, Fixed
;
Methacrylates
;
Polymethacrylic Acids
;
Tensile Strength
10.A Case of Eccrine Angiomatous Hamartoma.
Jae Chul LEE ; Jin Joo PARK ; Eun Chyung JUNG ; See Ryong PARK
Korean Journal of Dermatology 1988;26(2):255-258
Eccrine angiomatous hamartoma or sudoriparous angioma is a hamartoma in which histologically, hyperplasia of eccrine sweat apparatus and vascular elements is present in the same lesion and clinically has tenderness and hyperhidrosis over the lesion. We present a case of eccrine angiomatous hamartoma developed on the medial side of the right knee in a 5-year-old female patient.
Child, Preschool
;
Female
;
Hamartoma*
;
Hemangioma
;
Humans
;
Hyperhidrosis
;
Hyperplasia
;
Knee
;
Sweat