1.Thrombospondin-1 and -2 Expressions in Hepatocellular Carcinomas: an Association with Tumor Angiogenesis and p53 Overexpression.
Jae Sin CHUNG ; Ho Sung PARK ; Hyun Jin SON ; Myoung Jae KANG ; Woo Sung MOON
Korean Journal of Pathology 2005;39(4):215-221
Background : It has been suggested that thrombospondin (TSP) is a p53-dependent negative regulator of tumor angiogenesis. TSP expression and localization in hepatocellular carcinomas (HCCs) and its association with overexpression of p53 protein were investigated. Methods : TSP-1 and -2 expressions were examined in 40 HCC specimens by immunohistochemical staining and in 4 HCC cell lines by Western blotting. In addition, p53 protein expression and microvessel density (MVD) were correlated with the TSP expression. Results : Strong immu- nopositivity for TSP-1 was observed in fibroblasts, vascular endothelial cells, and some vas- cular smooth muscle cells of the stroma in 18 cases (45%), and in tumor cells in 3 cases (7.5%) of 40 cases of HCC. Immunoreactivity for TSP-2 was observed in only the sinusoidal lining cells of the tumor in 15 cases (46%), and in tumor cells in 2 cases (6%) of 32 cases of HCC. TSP-1 expression was inversely correlated with MVD (p=0.028), but TSP-2 expression did not show any correlation with MVD. Although p53 was overexpressed in 17 cases, there was no significant correlation between TSP and p53 expressions. None of the HCC cell lines expressed TSP-1 or -2. Conclusions : These findings indicate that TSP-1 is mainly derived from nonparenchymal cells, and may decrease tumor angiogenesis in HCC.
Angiogenesis Inhibitors
;
Blotting, Western
;
Carcinoma, Hepatocellular*
;
Cell Line
;
Endothelial Cells
;
Fibroblasts
;
Microvessels
;
Myocytes, Smooth Muscle
;
Thrombospondin 1
;
Thrombospondins
2.A Case of tuberous Sclerosis with Polycystic Kidney.
Won Ik LEE ; Il Sin MOON ; Poong Man LEE ; Jae Chung LEE
Journal of the Korean Pediatric Society 1981;24(11):1100-1105
No abstract available.
Polycystic Kidney Diseases*
;
Tuberous Sclerosis*
3.A Case Report of Agenesis of Gallbladder which was Diagnosed after an Emergent operation Due to Ostructive Jundice with Impacted CBD Stones.
Jae Sin CHUNG ; Yoon Seok CHAE ; Sung Soo OH ; Eul Sam CHUNG
Journal of the Korean Surgical Society 1997;52(6):907-911
A case of Agenesis of gallbladder in 73-year old female patient who had an emergent operation due to obstructive jaundice with impacted CBD stones is reported. The patient suffered from icteric sclera and abdominal pain which waxed and waned for three days. Impacted CBD stones and an agenesis of the gallbladder was suggested by a computed tomogram of the abdomen. In the operating field, multiple adhesions around the biliary tree was noticed, but we could not find the gallbladder and cystic duct. She underwent choledocholithotomy, T-tube choledochostomy, operative cholangiography, and drainage. Operative cholangiogaphy showed no remained stones, and there was no structures suggesting gallbladder and cystic duct. The authors described the case with a recent review from the literature.
Abdomen
;
Abdominal Pain
;
Aged
;
Biliary Tract
;
Cholangiography
;
Choledochostomy
;
Cystic Duct
;
Drainage
;
Female
;
Gallbladder*
;
Humans
;
Jaundice, Obstructive
;
Sclera
4.Relapse Rates of Ulcerative Colitis in Remission and Factors Related to Relapse.
Byoung Joon PARK ; Kwang Jae LEE ; Jae Chul HWANG ; Sung Jae SIN ; Jae Yeon CHUNG ; Sung Won CHO
The Korean Journal of Gastroenterology 2008;52(1):21-26
BACKGROUND/AIMS: Ulcerative colitis (UC) is a chronic inflammatory bowel disease with heterogeneous clinical features. Data on the disease course and prognosis of UC patients who have been regularly treated are lacking. We aimed to investigate relapse rates of UC in remission and factors related to relapse. METHODS: We retrospectively analyzed clinical courses of 84 patients (43 males, median age 43 years, ranged 20-73 years) diagnosed as UC at Ajou University Hospital between January 1997 and December 2005 based on clinical, endoscopic and pathologic findings, and who were regularly followed for at least one year after the remission. RESULTS: Study subjects consisted of 32 proctitis (38%), 21 left-sided colitis (25%), and 31 subtotal or total colitis (37%). Of 84 patients, relapse was observed in 52 patients (62%) during the follow-up period (ranged 1-9 years). The relapse rate was 24%, 41%, 51%, 65%, 71%, and 79% at 1 year, 2 years, 3 years, 4 years, 5 years and 6 years, respectively. Among sex, age, hemoglobin, ESR, and the extent of disease on admission, decrease of hemoglobin level was the only independent factor related to relapse (odds ratio=2.67, 95% CI (1.32-5.42), p<0.01). CONCLUSIONS: In Korea, relapse of UC in remission is not rare. Decrease of hemoglobin level is an independent risk factor related to its relapse, while the extent of disease is not.
Adult
;
Aged
;
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use
;
Antimetabolites/therapeutic use
;
Azathioprine/therapeutic use
;
Chronic Disease
;
Colitis, Ulcerative/*diagnosis/*epidemiology/therapy
;
Data Interpretation, Statistical
;
Female
;
Follow-Up Studies
;
Hemoglobins/analysis
;
Humans
;
Male
;
Mesalamine/therapeutic use
;
Middle Aged
;
Odds Ratio
;
Recurrence
;
Retrospective Studies
;
Risk Factors
;
Time Factors
5.Remote Postoperative Epidural Hematoma after Brain Tumor Surgery.
Ho Jung CHUNG ; Jae Sung PARK ; Jae Hyun PARK ; Sin Soo JEUN
Brain Tumor Research and Treatment 2015;3(2):132-137
A postoperative epidural hematoma (EDH) is a serious and embarrassing complication, which usually occurs at the site of operation after intracranial surgery. However, remote EDH is relatively rare. We report three cases of remote EDH after brain tumor surgery. All three cases seemed to have different causes of remote postoperative EDH; however, all patients were managed promptly and showed excellent outcomes. Although the exact mechanism of remote postoperative EDH is unknown, surgeons should be cautious of the speed of lowering intracranial pressure and implement basic procedures to prevent this hazardous complication of brain tumor surgery.
Brain Neoplasms*
;
Brain*
;
Craniotomy
;
Hematoma*
;
Humans
;
Intracranial Pressure
;
Neurosurgery
6.Combination Therapy for Gliomas Using Temozolomide and Interferon-Beta Secreting Human Bone Marrow Derived Mesenchymal Stem Cells.
Jae Hyun PARK ; Chung Heon RYU ; Mi Jin KIM ; Sin Soo JEUN
Journal of Korean Neurosurgical Society 2015;57(5):323-328
OBJECTIVE: Malignant gliomas are the most common primary tumors of the central nervous system and the prognosis of patients with gliomas is poor. The combination of interferon-bata (IFN-beta) and temozolomide (TMZ) has shown significant additive antitumor effects in human glioma xenograft models. Considering that the poor survival of patients with human malignant gliomas relates partly to the inability to deliver therapeutic agents to the tumor, the tropism of human bone marrow-derived mesenchymal stem cells (MSC) for malignant gliomas can be exploited to therapeutic advantages. We investigated the combination effects of TMZ and MSCs that secrete IFN-beta on gliomas. METHODS: We engineered human MSCs to secret mouse IFN-beta (MSC-IFN-beta) via adenoviral transduction and confirmed their secretory capacity using enzyme-linked immunosorbent assays. In vitro and in vivo experiments were performed to determine the effects of the combined TMZ and MSC-IFN-beta treatment. RESULTS: In vitro, the combination of MSC-IFN-beta and TMZ showed significantly enhanced antitumor effects in GL26 mouse glioma cells. In vivo, the combined MSC-IFN-beta and TMZ therapy significantly reduced the tumor size and improved the survival rates compared to each treatment alone. CONCLUSION: These results suggest that MSCs can be used as an effective delivery vehicle so that the combination of MSC-IFN-beta and TMZ could be considered as a new option for the treatment of malignant gliomas.
Animals
;
Bone Marrow*
;
Central Nervous System
;
Enzyme-Linked Immunosorbent Assay
;
Glioma*
;
Heterografts
;
Humans
;
Interferon-beta*
;
Mesenchymal Stromal Cells*
;
Mice
;
Prognosis
;
Survival Rate
;
Tropism
7.A case of acquired angioedema with C1 esterase inhibitor deficiency.
Chang Young HA ; Sun Sin KIM ; Hun Jong KIM ; Dong Suk HAN ; Jae Woong CHO ; Hyuck Jun CHUNG ; Hee Yeon KIM ; Dong Ho NAHM ; Hae Sim PARK
Journal of Asthma, Allergy and Clinical Immunology 1999;19(2):224-228
Angioedema is a well-demarcated localized edema involving the deeper layers of the skin, including the subcutaneous tissue. Angioedema occurs with Cl esterase inhibitor (Cl INH) deficiency that may be inborn as an autosomal dominant characteristic or may be acquired. Acquired angioedema (AAE) is a rare disorder characterized by adult onset and lack of evidence of inheritance of the disease. Two types of AAE are known today: type I in which there are lowering of functional Cl INH, an underlying disease such as a B-cell disease, and no detectable autoantibodies to Cl INH, type II with anti Cl INH autoantibodies in the circulation without detectable underlying disease and with depressed functional Cl INH levels. We experienced a case of angioedema in a 29-year old man. He had no family history of angioedema and laboratory data showed depressed Cl-INH levels. We diagnosed the case as acquired type of angioedema. Even though we could not measure anti-Cl INH auto-antibodies, we identified the case as type II because there was no evidence of underlying disease.
Adult
;
Angioedema*
;
Angioedemas, Hereditary*
;
Autoantibodies
;
B-Lymphocytes
;
Complement C1 Inhibitor Protein*
;
Complement C1s*
;
Edema
;
Humans
;
Skin
;
Subcutaneous Tissue
;
Wills
8.Disseminated Hemangioblastoma of the Central Nervous System without Von Hippel-Lindau Disease.
Sun Yoon CHUNG ; Sin Soo JEUN ; Jae Hyun PARK
Brain Tumor Research and Treatment 2014;2(2):96-101
Hemangioblastoma (HB) of the central nervous system may occur sporadically or in association with von Hippel-Lindau (VHL) disease. Disseminated HB means malignant spread of the original primary HB without local recurrence at surgically resected site. It has been rarely reported previously, and rarer especially without VHL gene mutation. We report a case of disseminated HB without VHL disease. A 59-year-old man underwent a surgery for total removal of a cerebellar HB. From five years after the surgery, multiple dissemination of HB was identified intracranially and he subsequently underwent cyberknife radiosurgery. The lesions got smaller temporarily, but they soon grew larger. Nine years after the initial surgery for cerebellar HB, he showed severe back pain. His magnetic resonance image of spine revealed intradural extramedullary mass at T6-7 level. Complete surgical removal of the mass was performed and the pathological diagnosis was identical to the previous one. He had no evidence of VHL disease. And there was no recurrence of the tumor at the site of the original operation. The exact mechanism of dissemination is unknown, but the surgeon should be cautious of tumor cell spillage during surgery and prudently consider the decision to perform ventriculo-peritoneal shunt. In addition, continuous follow-up for recurrence or dissemination is necessary for patients even who underwent complete removal of cerebellar HB.
Back Pain
;
Central Nervous System*
;
Diagnosis
;
Hemangioblastoma*
;
Humans
;
Middle Aged
;
Radiosurgery
;
Recurrence
;
Spine
;
Ventriculoperitoneal Shunt
;
von Hippel-Lindau Disease*
9.studies of Osseointegrated Implant-Models on Stress Distribution.
Chong Hyun HAN ; Hung Jae CHUN ; Sin Young JUNG ; Seong Joo HEO ; Chong Pyung CHUNG ; Young KU ; In Chul RYU ; Yong Chang CHOI ; Myung Ho KIM
The Journal of Korean Academy of Prosthodontics 2000;38(4):526-543
Finite element analyses were performed to study effects on stress distribution generated in jaw bone for various shapes of dental implants: plateau type, plateau with small radius of curvature, triangular thread screw type in accordance with ISO regulations and square thread screw filleted with small radius partially. It was found that square thread screw filleted with small radius was more effective on stress distribution than other dental implants used in analyses. Additional analyses were performed on the implant with square thread screw filleted with small radius for verying design parameters, such as the width of thread end, the height of the thread of the implant and load direction, to determine the optimum dimensions of the implant. The highest stress concentration occurred at the region in jaw bone adjacent to the first thread of the implant. The maximum effective stress induced by a 15 degree oblique load of 100 N was twice as high as the maximum effective stress caused by an equal amount of vertical load. Stress distribution was more effective in the case when the width of thread end and the height of thread were p/2 and 0.46p, respectively, where p is the pitch of thread. At last, using tensile force calculated from the possible insert torque without breading bone thread, finite element analysis was performed on the implant to calculate pre-stress when the primary fixation of the implant was operated in jaw bone. The maximum effective stress was 136.8 MPa which proven to be safe.
Bread
;
Dental Implants
;
Finite Element Analysis
;
Jaw
;
Radius
;
Social Control, Formal
;
Torque
10.Mutational Analysis of FOXL2 Gene in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome (BPES) Patients.
Sin Chul KIM ; Soon Cheol CHA ; Wha Sun CHUNG ; Yeon Sil JANG ; Jae Ryong KIM
Journal of the Korean Ophthalmological Society 2003;44(5):1172-1179
PURPOSE: The purpose of this paper is to identify the forkhead transcription factor gene (FOXL2) mutations in Korean patients with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). METHODS: We have analyzed the mutations of FOXL2 gene in genomic DNAs extracted from 16 BPES patients and their families by PCR, PCR-SSCP, and sequencing. RESULTS: No deletion in exon 1 to 3 of the FOXL2 gene was observed by PCR. The PCR products were subjected to SSCP analysis and 9 patients showed SSCP shifts. The PCR products showing SSCP shifts were subcloned into plasmid vectors and sequenced to confirm the FOXL2 mutation. In total, 7 mutations (1 nonsense mutation, 1 deletion, and 5 duplications) in exon 2 were identified. CONCLUSIONS: The FOXL2 gene mutations were identified in the Korean BPES patients. Some of the mutations were previously reported and some were new mutations. This study will contribute to the molecular analysis and clinical counseling of BPES patients.
Codon, Nonsense
;
Counseling
;
DNA
;
Exons
;
Humans
;
Plasmids
;
Polymerase Chain Reaction
;
Polymorphism, Single-Stranded Conformational
;
Transcription Factors