1.Silibinin Enhances Ultraviolet B-Induced Apoptosis in MCF-7 Human Breast Cancer Cells.
Eun Mi NOH ; Mi Suk YI ; Hyun Jo YOUN ; Byoung Kil LEE ; Young Rae LEE ; Ji Hey HAN ; Hong Nu YU ; Jong Suk KIM ; Sung Hoo JUNG
Journal of Breast Cancer 2011;14(1):8-13
PURPOSE: Chemotherapies for breast cancer generally have strong cellular cytotoxicity and severe side effects. Thus, significant emphasis has been placed on combinations of naturally occurring chemopreventive agents. Silibinin is a major bioactive flavonolignan extracted from milk thistle with chemopreventive activity in various organs including the skin, prostate, and breast. However, the mechanism underlying the inhibitory action of silibinin in breast cancer has not been completely elucidated. Therefore, we investigated the effect of silibinin in MCF-7 human breast cancer cells and determined whether silibinin enhances ultraviolet (UV) B-induced apoptosis. METHODS: The effects of silibinin on MCF-7 cell viability were determined using the MTT assay. The effect of silibinin on PARP cleavage, as the hallmark of apoptotic cell death, and p53 protein expression in MCF-7 cells was analyzed using Western blot. The effect of silibinin on UVB-induced apoptosis in MCF-7 cells was analyzed by flow cytometry. RESULTS: A dose- and time-dependent reduction in viability was observed in MCF-7 cells treated with silibinin. Silibinin strongly induced apoptotic cell death in MCF-7 cells, and induction of apoptosis was associated with increased p53 expression. Moreover, silibinin enhanced UVB-induced apoptosis in MCF-7 cells. CONCLUSION: Silibinin induced a loss of cell viability and apoptotic cell death in MCF-7 cells. Furthermore, the combination of silibinin and UVB resulted in an additive effect on apoptosis in MCF-7 cells. These results suggest that silibinin might be an important supplemental agent for treating patients with breast cancer.
Apoptosis
;
Blotting, Western
;
Breast
;
Breast Neoplasms
;
Cell Death
;
Cell Survival
;
Humans
;
MCF-7 Cells
;
Milk Thistle
;
Prostate
;
Silymarin
;
Skin
2.Effects of Endotracheal Intubation on the Temporomandibular Joint.
In Sun JUNG ; Sung Suk NOH ; Du Sik SON ; Bae Hee JUNG ; Mi Hwa JUNG ; Rim Soo WON
Korean Journal of Anesthesiology 1995;28(1):73-82
Tracheal intubation for general anesthesia is usually performed using a rigid laryngoscope and reguires the mandible to be opened with forward and upward traction of the patient's jaw which may at times result in the inadvertant injury to temporomandibular joint(TMJ). The injury may include internal derangement, dislocation and hematoma of TMJ; subsequent intraarticular adhesion formation ; dislocation of the meniscus, and rarely auriculotemporal nerve damage from traumatic TMJ dislocation. We studied in 200 patients the size of mouth opening during intubation, the change of mouth opening by tracheal intubation evaluated after operation, and any TMJ disorder arising after tracheal intubation. The results were as follows; 1) The mean size of mouth opening before operation was 42.7+/-7.0 and 40.6+/-6.2mm in male and female patients, respectively. 2) The mean size of mouth opening during intubation was 24.7+/-2.6 and 23.4+/-2.7mm in male and female patients, respectively. When vecuronium was used to prevent fasciculation, the mean was 24.3+/-3.1 and 25.2+/-2.0mm in male and female patients, respectively. 3) One week following operation The mean size of mouth opening one week postoperation was 48.3+/-8.9 and 42.2+/-6.3mm in male and female patients, respectively. When vecuronium was used to prevent fasciculation, the mean size of mouth opening was 55.5+/-5.3 and 43.2+/-6.2mm in male and female patients, respectively. 4) Five patients complained of discomfort around TMJ after tracheal intubation. It seems that upward 45 mandibule lifting by laryngoscope caused trauma to TMJs.
Anesthesia, General
;
Dislocations
;
Fasciculation
;
Female
;
Hematoma
;
Humans
;
Intubation
;
Intubation, Intratracheal*
;
Jaw
;
Laryngoscopes
;
Lifting
;
Male
;
Mandible
;
Mouth
;
Temporomandibular Joint Disorders
;
Temporomandibular Joint*
;
Traction
;
Vecuronium Bromide
3.A Study on Viral Hepatitis Markers and Abnormal Liver Function Test in Adults Living in Northwest Area of Chungnam.
Suk Bae KIM ; Won Kyung LEE ; Hoon CHOI ; So Mi KIM ; Rhan NOH ; Ha Yan KANG ; Sang Suk LEE ; Sung Soo RA ; Jae Hwan GONG ; Hyun Duk SHIN
The Korean Journal of Gastroenterology 2009;53(6):355-360
BACKGROUND/AIMS: We studied the prevalence of chronic hepatitis B, C and abnormality on liver function among the population in northwest area of Chungnam. METHODS: We have reviewed 40,112 adults who had received medical examination at health promotion center in Dankook university hospital. We studied them retrospectively about HBsAg, HBsAb, anti-HCV, and liver function test (LFT). RESULTS: Among the study subjects, 22,936 men and 17,176 women were involved. The overall seroprevalence of HBsAg was 4.2%. The prevalence in men (4.5%) was higher than that of women (3.7%) (p<0.001). The seroprevalence of HBsAg in their age was 5.1% in the 5th decade, 4.2% in the 2nd decade, 4.1% in the 4th decade, and 4.1% in the 6th decade. The overall seroprevalence of HBsAb was 65.1%. The overall seroprevalence of anti-HCV was 0.7%. After we reexamined them with HCV RNA or RIBA (Recombinant Immunoblot Assay), the prevalence of chronic hepatitis C was 0.09%. The LFT abnormality in total subjects was 11.4%. The LFT abnormality of chronic hepatitis B and C subjects was 21.72% and 63.2%. CONCLUSIONS: The prevalence of chronic hepatitis B and C was lower than that of previous studies. The prevalence of chronic hepatitis B in the 2nd decade was still high.
Adolescent
;
Adult
;
Aged
;
Aged, 80 and over
;
Child
;
Female
;
Hepatitis B Antibodies/blood
;
Hepatitis B Surface Antigens/blood
;
Hepatitis B, Chronic/*epidemiology/immunology/physiopathology
;
Hepatitis C Antibodies/blood
;
Hepatitis C, Chronic/*epidemiology/immunology/physiopathology
;
Humans
;
Korea
;
Liver Function Tests
;
Male
;
Middle Aged
;
Prevalence
;
RNA, Viral/blood
;
Retrospective Studies
4.A Case of Secondary Syphilis with Jarisch-Herxheimer Reaction Presenting as Hypersensitivity Pneumonit.
Jung Yeon HEO ; Ji Yoon NOH ; Mi Jung KIM ; Yu Mi JO ; Won Suk CHOI ; Joon Young SONG ; Hee Jin CHEONG ; Woo Joo KIM
Infection and Chemotherapy 2009;41(5):298-300
Jarisch-Herxheimer reaction (JHR) is a self-limited, acute febrile hypersensitivity reaction that occurs after antibiotic therapy against spirochetes disease. When occurring in the text of syphilis therapy, the JHR begins typically 1-2 hour after the administration of penicillin and is characterized by fever, chills, myalgias, and exacerbation of skin lesions. Rarely, severe JHR can occur in the form of endocarditis, fulminant hepatitis, and hypersensitivity pneumonitis. Recently, we experienced an interesting case of JHR complicated by the hypersensitivity pneumonitis after treating secondary syphilis. Proper differential diagnosis is required to differentiate this reaction from drug-induced hypersensitivity reaction.
Alveolitis, Extrinsic Allergic
;
Chills
;
Diagnosis, Differential
;
Endocarditis
;
Fever
;
Hepatitis
;
Hypersensitivity
;
Penicillins
;
Skin
;
Spirochaetales
;
Syphilis
5.A Case of Secondary Syphilis with Jarisch-Herxheimer Reaction Presenting as Hypersensitivity Pneumonit.
Jung Yeon HEO ; Ji Yoon NOH ; Mi Jung KIM ; Yu Mi JO ; Won Suk CHOI ; Joon Young SONG ; Hee Jin CHEONG ; Woo Joo KIM
Infection and Chemotherapy 2009;41(5):298-300
Jarisch-Herxheimer reaction (JHR) is a self-limited, acute febrile hypersensitivity reaction that occurs after antibiotic therapy against spirochetes disease. When occurring in the text of syphilis therapy, the JHR begins typically 1-2 hour after the administration of penicillin and is characterized by fever, chills, myalgias, and exacerbation of skin lesions. Rarely, severe JHR can occur in the form of endocarditis, fulminant hepatitis, and hypersensitivity pneumonitis. Recently, we experienced an interesting case of JHR complicated by the hypersensitivity pneumonitis after treating secondary syphilis. Proper differential diagnosis is required to differentiate this reaction from drug-induced hypersensitivity reaction.
Alveolitis, Extrinsic Allergic
;
Chills
;
Diagnosis, Differential
;
Endocarditis
;
Fever
;
Hepatitis
;
Hypersensitivity
;
Penicillins
;
Skin
;
Spirochaetales
;
Syphilis
6.Effect of High Glucose on Nitric Oxide Production in Culteured Rat Mesangial Cells.
Hyun Jin NOH ; Hun Joo HA ; Mi Ra YOO ; Suk Kyun SHIN ; Hyun Yong SONG ; Jae Ha HWANG ; Shin Wook KANG ; Kyu Heon CHOI ; Dae Seok HAN ; Ho Young LEE
Korean Journal of Nephrology 1999;18(6):856-868
Diabetic nephopathy is one of the leading causes of end-stage renal disease and characterized pathologically by the glomerular mesangial expansion and increased extracellular matrix(ECM) formation. Glomerular hyper-filtration and increased vascular permeability observed in the early stage of diabetic nephropathy have been proposed to play a significant pathophysiologic role in the eventual development of glomerulosclerosis of dia-betic nephropathy. Some studies have suggested that this glomerular hyperfiltration is mediated by increased nitric oxide(NO) production via the constitutive nitric oxide synthase(cNOS) pathway present in endothelial cells under the high glucose environment. However, the exact role of the inducible NOS(iNOS) pathway present in mesangial cells in the pathogenesis of diabetic neph-ropathy is not clearly established. The present study was carried out to examine whether NO production via the iNOS pathway is mo-dulated in cultured rat mesangial cells exposed to the high glucose environment and underlying mechanism of this modulation. For this purpose, the production of the stable metabolite of NO(nitrite), intracellular cyclic gu-anosine monophosphate(cGMP), iNOS mRNA expression and iNOS protein synthesis were examined under different glucose concentrations. Rat mesangial cells cultured in high glucose concen- tration(30mM D-glucose) increased significantly nitrit#e/ nitrate production and intracellular cGMP levels upon stimulation with lipopolysaccharide(LPS) plus interfer-on-r (IFN-r ) compared with control glucose concen- tration(5.6mM D-glucose). Mesangial iNOS mRNA expression and protein synthesis also increased signifi- cantly in response to high glucose. This enhanced iNOS mRNA expression induced by high glucose concentration was significantly suppressed by protein kinase C(PKC) inhibitor, calphostin C, and the aldose reductase inhibitor, 6-bromo-l, 3-dioxo-1H- benz[d, elisoquinoline-2(3H)-acetic acid. These results indicate that high glucose in combination with stimulation by LPS plus IFN- r enhances NO production from mesangial cells by the iNOS pathway, and that the activation of PKC and the polyol pathway may play a role in this enhancement.
Aldehyde Reductase
;
Animals
;
Capillary Permeability
;
Diabetic Nephropathies
;
Endothelial Cells
;
Glucose*
;
Kidney Failure, Chronic
;
Mesangial Cells*
;
Nitric Oxide*
;
Protein Kinases
;
Rats*
;
RNA, Messenger
7.Candida Spondylodiscitis with Epidural Abscess Treated with Voriconazole.
Ji Yun NOH ; Jung Yeon HEO ; Won Suk CHOI ; Yu Mi JO ; Joon Young SONG ; Hee Jin CHEONG ; Woo Joo KIM
Korean Journal of Medical Mycology 2009;14(3):145-149
Candida spondylodiscitis with epidural abscess is rarely reported and known to be the late complication of candidemia. A 48-years-old man presented with 4 weeks of progressively aggravating low back pain. He had a history of fungemia caused by Candida albicans 4 months earlier, for which he had been treated successfully with systemic fluconazole. The MRI of lumbar spine demonstrated the spondylodiscitis with multiple epidural abscesses at the L2/3 level. Along with the surgical interventions including abscess drainage, the intravenous amphotericin B administration was begun. Culture of drained pus yielded the growth of Candida albicans. After therapy with parenteral amphotericin B for 2 weeks followed by oral fluconazole for 8 weeks, the back pain resolved. However the low back pain and inflammation relapsed during oral fluconazole therapy. Thereafter oral voriconazole had been administered for 24 weeks and the patient showed complete recovery and no recurrence.
Abscess
;
Amphotericin B
;
Back Pain
;
Candida
;
Candida albicans
;
Candidemia
;
Discitis
;
Drainage
;
Epidural Abscess
;
Fluconazole
;
Fungemia
;
Humans
;
Inflammation
;
Low Back Pain
;
Pyrimidines
;
Recurrence
;
Spine
;
Suppuration
;
Triazoles
8.Candida Spondylodiscitis with Epidural Abscess Treated with Voriconazole.
Ji Yun NOH ; Jung Yeon HEO ; Won Suk CHOI ; Yu Mi JO ; Joon Young SONG ; Hee Jin CHEONG ; Woo Joo KIM
Korean Journal of Medical Mycology 2009;14(3):145-149
Candida spondylodiscitis with epidural abscess is rarely reported and known to be the late complication of candidemia. A 48-years-old man presented with 4 weeks of progressively aggravating low back pain. He had a history of fungemia caused by Candida albicans 4 months earlier, for which he had been treated successfully with systemic fluconazole. The MRI of lumbar spine demonstrated the spondylodiscitis with multiple epidural abscesses at the L2/3 level. Along with the surgical interventions including abscess drainage, the intravenous amphotericin B administration was begun. Culture of drained pus yielded the growth of Candida albicans. After therapy with parenteral amphotericin B for 2 weeks followed by oral fluconazole for 8 weeks, the back pain resolved. However the low back pain and inflammation relapsed during oral fluconazole therapy. Thereafter oral voriconazole had been administered for 24 weeks and the patient showed complete recovery and no recurrence.
Abscess
;
Amphotericin B
;
Back Pain
;
Candida
;
Candida albicans
;
Candidemia
;
Discitis
;
Drainage
;
Epidural Abscess
;
Fluconazole
;
Fungemia
;
Humans
;
Inflammation
;
Low Back Pain
;
Pyrimidines
;
Recurrence
;
Spine
;
Suppuration
;
Triazoles
9.Arthroscopic Synovectomy in a Patient with Primary Hypertrophic Osteoarthropathy.
Jaejoon LEE ; Hyungjin KIM ; Ji Won HWANG ; Jung Won NOH ; Joong Kyung AHN ; Eun Mi KOH ; Hoon Suk CHA
The Journal of the Korean Rheumatism Association 2008;15(3):261-267
No abstract available.
10.Proteomics Analysis for Helicobacter pylori-infected Gastric Mucosa.
Ho Suk KANG ; Sung Noh HONG ; Hye Rim PARK ; Mi Jung KWON ; Jun Haeng LEE ; Jae J KIM
The Korean Journal of Gastroenterology 2014;64(1):10-17
BACKGROUND/AIMS: Helicobacter pylori infection is linked to the development of gastric cancer. H. pylori-associated gastric inflammation is considered to be the first important step in the histogenesis of such neoplasia. However, studies that compare proteome of gastric mucosa infected with or without H. pylori are lacking. METHODS: We employed proteomics analysis on the endoscopic biopsy specimens of gastric mucosa obtained from two groups (30 cases): healthy subjects without H. pylori infection (15 cases), and gastritis patients with H. pylori infection (15 cases). The pooled proteins obtained from gastric mucosa infected with or without H. pylori were separated by two-dimensional gel electrophoresis and analyzed by a computer-aided program. The altered protein expressions were then identified by mass spectrometry and validated by Western blotting and immunohistochemistry. RESULTS: On mass spectrometry using MALDI TOF(TM) Analyzer, the up-regulation of Keratin 1, ezrin, adenosine triphosphate (ATP) synthase subunit alpha mitochondrial isoform c, Keratin type I cytoskeletal 19, and Keratin type I cytoskeletal 9 were identified; in contrast, 71 kd heat shock cognate protein, ATP synthase subunit alpha mitochondrial precursor, and annexin IV were down-regulated. Among them, membrane cytoskeleton linker ezrin was validated using Western blot and immunohistochemistry. CONCLUSIONS: Expression of ezrin was significantly different between the gastric mucosa with and without H. pylori infection. Therefore, ezrin could be considered a promising potential molecular marker for detecting H. pylori infection in gastric mucosa.
Blotting, Western
;
Cytoskeletal Proteins/metabolism
;
Down-Regulation
;
Electrophoresis, Gel, Two-Dimensional
;
Female
;
Gastric Mucosa/*metabolism/microbiology
;
Gastritis/complications/metabolism/pathology
;
Gastroscopy
;
Helicobacter Infections/complications/metabolism/*pathology
;
*Helicobacter pylori
;
Humans
;
Immunohistochemistry
;
Male
;
Proteome/*analysis
;
*Proteomics
;
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
;
Up-Regulation