1.The effect of isochromosome 17q presence, proliferative and apoptotic indices, expression of c-erbB-2, bcl-2 and p53 proteins on the prognosis of medulloblastoma.
Do Hyun NAM ; Kyu Chang WANG ; Yoen Mee KIM ; Je G CHI ; Seung Ki KIM ; Byung Kyu CHO
Journal of Korean Medical Science 2000;15(4):452-456
Medulloblastoma accounts for 20 to 25+ACU- of all intracranial neoplasms in children. The significance of the presence of isochromosome 17q (i(17q)), proliferative potential, apoptotic activity, and expression of c-erbB-2, bd-2, and p53 proteins in predicting long-term survival of patients with medulloblastomas was investigated. Twenty children were divided into two groups (favorable and poor outcome groups). Ten children with favorable outcome (FO) were disease-free during the follow-up period (median: 61.5 months). The other ten children with poor outcome (PO) died of disease progression, having a median survival of 18 months. Fluorescent in situ hybridization (FISH) for i(17q), terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL), and immunohistochemistry for Ki-67, c-erbB-2, bcl-2, and p53 proteins was performed in these patients. Nine out of 17 children showed i(17q). There was no difference in the rate of positive i(17q) between the FO and PO groups. The presence of i(17q) was not significantly related to biological factors that we investigated. Unlike the prominent presence of the proliferative potential and p53 expression in children with PO, apoptotic activity and expression of c-erbB-2 and bcl-2 had no correlation with the outcome.
Adolescence
;
Apoptosis
;
Brain Neoplasms/pathology
;
Brain Neoplasms/mortality
;
Brain Neoplasms/genetics+ACo-
;
Cell Division
;
Child
;
Child, Preschool
;
Chromosomes, Human, Pair 17/ultrastructure+ACo-
;
Chromosomes, Human, Pair 17/genetics
;
Comparative Study
;
Disease-Free Survival
;
Female
;
Follow-Up Studies
;
Genes, bcl-2+ACo-
;
Genes, erbB-2+ACo-
;
Genes, p53+ACo-
;
Human
;
In Situ Hybridization, Fluorescence
;
In Situ Nick-End Labeling
;
Infant
;
Ki-67 Antigen/analysis
;
Male
;
Medulloblastoma/pathology
;
Medulloblastoma/mortality
;
Medulloblastoma/genetics+ACo-
;
Neoplasm Proteins/analysis
;
Prognosis
;
Retrospective Studies
;
Survival Analysis
;
Treatment Outcome
2.The effect of isochromosome 17q presence, proliferative and apoptotic indices, expression of c-erbB-2, bcl-2 and p53 proteins on the prognosis of medulloblastoma.
Do Hyun NAM ; Kyu Chang WANG ; Yoen Mee KIM ; Je G CHI ; Seung Ki KIM ; Byung Kyu CHO
Journal of Korean Medical Science 2000;15(4):452-456
Medulloblastoma accounts for 20 to 25+ACU- of all intracranial neoplasms in children. The significance of the presence of isochromosome 17q (i(17q)), proliferative potential, apoptotic activity, and expression of c-erbB-2, bd-2, and p53 proteins in predicting long-term survival of patients with medulloblastomas was investigated. Twenty children were divided into two groups (favorable and poor outcome groups). Ten children with favorable outcome (FO) were disease-free during the follow-up period (median: 61.5 months). The other ten children with poor outcome (PO) died of disease progression, having a median survival of 18 months. Fluorescent in situ hybridization (FISH) for i(17q), terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL), and immunohistochemistry for Ki-67, c-erbB-2, bcl-2, and p53 proteins was performed in these patients. Nine out of 17 children showed i(17q). There was no difference in the rate of positive i(17q) between the FO and PO groups. The presence of i(17q) was not significantly related to biological factors that we investigated. Unlike the prominent presence of the proliferative potential and p53 expression in children with PO, apoptotic activity and expression of c-erbB-2 and bcl-2 had no correlation with the outcome.
Adolescence
;
Apoptosis
;
Brain Neoplasms/pathology
;
Brain Neoplasms/mortality
;
Brain Neoplasms/genetics+ACo-
;
Cell Division
;
Child
;
Child, Preschool
;
Chromosomes, Human, Pair 17/ultrastructure+ACo-
;
Chromosomes, Human, Pair 17/genetics
;
Comparative Study
;
Disease-Free Survival
;
Female
;
Follow-Up Studies
;
Genes, bcl-2+ACo-
;
Genes, erbB-2+ACo-
;
Genes, p53+ACo-
;
Human
;
In Situ Hybridization, Fluorescence
;
In Situ Nick-End Labeling
;
Infant
;
Ki-67 Antigen/analysis
;
Male
;
Medulloblastoma/pathology
;
Medulloblastoma/mortality
;
Medulloblastoma/genetics+ACo-
;
Neoplasm Proteins/analysis
;
Prognosis
;
Retrospective Studies
;
Survival Analysis
;
Treatment Outcome
3.Loss of ARID1A Expression in Gastric Cancer: Correlation with Mismatch Repair Deficiency and Clinicopathologic Features.
Kyung Ju KIM ; Hae Yoen JUNG ; Mee Hye OH ; Hyundeuk CHO ; Ji Hye LEE ; Hyun Ju LEE ; Si Hyong JANG ; Moon Soo LEE
Journal of Gastric Cancer 2015;15(3):201-208
PURPOSE: The AT-rich interactive domain 1A (ARID1A) gene encodes BRG1-associated factor 250a, a component of the SWItch/Sucrose NonFermentable chromatin remodeling complex, which is considered a tumor suppressor in many tumors. We aimed to investigate the prognostic significance of ARID1A expression in gastric cancers and explore its relationship with clinicopathologic parameters such as mismatch repair protein expression. MATERIALS AND METHODS: Four tissue microarrays were constructed from 191 resected specimens obtained at Soonchunhyang University Cheonan Hospital from 2006 to 2008. Nuclear expression of ARID1A was semiquantitatively assessed and binarized into retained and lost expression. RESULTS: Loss of ARID1A expression was observed in 62 cases (32.5%). This was associated with more frequent vascular invasion (P=0.019) and location in the upper third of the stomach (P=0.001), and trended toward more poorly differentiated subtypes (P=0.054). ARID1A loss was significantly associated with the mismatch repair-deficient phenotype (P=0.003). ARID1A loss showed a statistically significant correlation with loss of MLH1 (P=0.001) but not MSH2 expression (P=1.000). Kaplan-Meier survival analysis showed no statistically significant difference in overall survival; however, patients with retained ARID1A expression tended to have better overall survival than those with loss of ARID1A expression (P=0.053). In both mismatch repair-deficient and mismatch repair-proficient groups, survival analysis showed no differences related to ARID1A expression status. CONCLUSIONS: Our results demonstrated that loss of ARID1A expression is closely associated with the mismatch repair-deficient phenotype, especially in sporadic microsatellite instability-high gastric cancers.
Chromatin Assembly and Disassembly
;
Chungcheongnam-do
;
DNA Mismatch Repair*
;
Humans
;
Microsatellite Instability
;
Microsatellite Repeats
;
Phenotype
;
Stomach
;
Stomach Neoplasms*
4.Mediastinal Glomus Tumor: A Case Report and Literature Review.
Si Hyong JANG ; Hyun Deuk CHO ; Ji Hye LEE ; Hyun Ju LEE ; Hae Yoen JUNG ; Kyung Ju KIM ; Sung Sik CHO ; Mee Hye OH
Journal of Pathology and Translational Medicine 2015;49(6):520-524
A glomus tumor in the mediastinum is very uncommon, and only five cases have been reported in the English literature. We recently encountered a 21-year-old woman with an asymptomatic mediastinal mass that measured 5.3 x 4.0 cm. Surgical excision was performed, and the tumor was finally diagnosed as mediastinal glomus tumor with an uncertain malignant potential. After reviewing this case and previous reports, we analyzed the clinicopathologic features associated with progression of such a tumor.
Female
;
Glomus Tumor*
;
Humans
;
Mediastinum
;
Young Adult
5.Depression and Self-care Behavior in Patients with Diabetes Mellitus.
Su Yoen KIM ; Jae Ho LEE ; Ha Neul KIM ; Dong Kyu KIM ; Young NA ; Guil Sun KIM ; Mee Kyoung KIM ; Ki Hyun BAEK ; Moo IL KANG ; Kwang Woo LEE ; Ki Ho SONG
Korean Diabetes Journal 2009;33(5):432-438
BACKGROUND: Depression is known to be a risk factor for type 2 diabetes mellitus. Conversely, diabetes is also a risk factor for depression, and patients with diabetes have nearly twice the risk of comorbid depression as the general population. Depression in patients with diabetes may cause poor clinical outcomes through lower adherence to self-care activities such as exercise, diet control, and glucose monitoring. Furthermore, diabetic patients with depression are more likely to suffer from microvascular or macrovascular complications. We explored the prevalence of major depressive disorder in Korean diabetic patients and its impact on self-care activities and glucose control. METHODS: We surveyed depressive symptoms and self-care activities in 191 type 2 diabetic patients from the outpatient clinic of the St. Mary's hospital. Two questionnaires were used for assessment, the Harvard Department of Psychiatry/National Depression Screening Day Scale (HANDS) and the Summary of Diabetes Self-Care Activities (SDSCA). RESULTS: Of the 191 respondents who completed questionnaires, 39 (20.4%) patients were categorized as having major depressive disorder. Among the depressed patients, only six (15.3%) had been previously evaluated and managed for their psychiatric problems. The incidence of depression was significantly higher in female diabetic patients compared to patients without depression (74.4% vs. 45.4%, P<0.001). Patients with depression showed significantly poorer diet control (18.5 vs. 15.9, P = 0.046) and less glucose monitoring (4.1 vs. 2.7, P = 0.047). However, there were no differences in exercise, foot care, or smoking status between the two groups. Additionally, metabolic parameters such as HbA1C and lipid profile were not significantly different between the two groups. CONCLUSION: Many diabetic patients are suffering from depression and exhibit poorer self-care activities than patients without depression. Identifying and managing depressed diabetic patients may help improve their self-care activities.
Ambulatory Care Facilities
;
Surveys and Questionnaires
;
Depression
;
Depressive Disorder, Major
;
Diabetes Complications
;
Diabetes Mellitus
;
Diabetes Mellitus, Type 2
;
Diet
;
Female
;
Foot
;
Glucose
;
Humans
;
Incidence
;
Mass Screening
;
Prevalence
;
Risk Factors
;
Self Care
;
Smoke
;
Smoking
;
Stress, Psychological
6.Loss of Tumor Suppressor ARID1A Protein Expression Correlates with Poor Prognosis in Patients with Primary Breast Cancer.
Hyun Deuk CHO ; Jong Eun LEE ; Hae Yoen JUNG ; Mee Hye OH ; Ji Hye LEE ; Si Hyong JANG ; Kyung Ju KIM ; Sun Wook HAN ; Sung Yong KIM ; Han Jo KIM ; Sang Byung BAE ; Hyun Ju LEE
Journal of Breast Cancer 2015;18(4):339-346
PURPOSE: Somatic mutations of the chromatin remodeling AT-rich interactive domain 1A (SWI-like) gene (ARID1A) have been identified in many human cancers, including breast cancer. The purpose of this study was to evaluate the nuclear expression of ARID1A in breast cancers by immunohistochemistry (IHC) and to correlate the findings to clinicopathologic variables including prognostic significance. METHODS: IHC was performed on tissue microarrays of 476 cases of breast cancer. Associations between ARID1A expression and clinicopathologic characteristics and molecular subtype were retrospectively analyzed. RESULTS: Low expression of ARID1A was found in 339 of 476 (71.2%) cases. Low expression of ARID1A significantly correlated with positive lymph node metastasis (p=0.027), advanced pathologic stage (p=0.001), low Ki-67 labeling index (p=0.003), and negative p53 expression (p=0.017). The ARID1A low expression group had significantly shorter disease-free and overall survival than the ARID1A high expression group (p<0.001 and p<0.001, respectively). Multivariate analysis demonstrated that low expression of ARID1A was a significant independent predictive factor for poor disease-free and overall survival in patients with breast cancer (disease-free survival: hazard ratio, 0.38, 95% confidence interval [CI], 0.20-0.73, p=0.004; overall survival: hazard ratio, 0.11, 95% CI, 0.03-0.46, p=0.003). In patients with luminal A type disease, patients with low ARID1A expression had significantly shorter disease-free and overall survival rates than patients with high ARID1A expression (p=0.022 and p=0.018, respectively). CONCLUSION: Low expression of ARID1A is an independent prognostic factor for disease-free and overall survival in breast cancer patients and may be associated with luminal A type disease. Although the biologic function of ARID1A in breast cancer remains unknown, low expression of ARID1A can provide valuable prognostic information.
Breast Neoplasms*
;
Breast*
;
Chromatin Assembly and Disassembly
;
Humans
;
Immunohistochemistry
;
Lymph Nodes
;
Multivariate Analysis
;
Neoplasm Metastasis
;
Phenobarbital
;
Prognosis*
;
Retrospective Studies
;
Survival Rate