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1.
Biomarkers ; 19(1): 16-21, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24283984

ABSTRACT

OBJECTIVE: The aim of this study is to validate and investigate the clinical value of urinary enolase I in patients with endometriosis. METHODS: Urine samples of 39 patients with histologically confirmed endometriosis and 20 patients without endometriosis were collected. Western blot analysis and enzyme-linked immunosorbent assay were used to detect the increase of enolase I in patients' urine. RESULTS: Urinary enolase I expression corrected for creatinine ratio (non neuronal enolase (NNE)-Cr) was significantly greater in patients with endometriosis (p = 0.026). When the diagnostic performance of NNE-Cr was evaluated with serum CA-125 combination, the area under the curve was 0.821 (95% confidence interval 0.713-0.928) with sensitivity and specificity of 76.9% and 85.0%, respectively. CONCLUSION: Elevated urinary enolase I, in conjunction with serum CA-125, may be used as a potential biomarker for endometriosis.


Subject(s)
Biomarkers, Tumor/urine , DNA-Binding Proteins/urine , Endometriosis/urine , Phosphopyruvate Hydratase/urine , Tumor Suppressor Proteins/urine , Adult , Biomarkers/urine , CA-125 Antigen/blood , Case-Control Studies , Creatinine/urine , Endometriosis/diagnosis , Endometriosis/enzymology , Female , Humans , ROC Curve
2.
Gynecol Obstet Invest ; 75(4): 268-74, 2013.
Article in English | MEDLINE | ID: mdl-23571154

ABSTRACT

OBJECTIVES: To compare plasma kisspeptin, serum leptin, and serum retinol-binding protein 4 (RBP4) levels in women with and without polycystic ovary syndrome (PCOS) and to correlate these among each other and with clinical, hormonal, and metabolic parameters. METHODS: Ninety women, including 54 women with PCOS and 36 without PCOS, participated in this study. For all patients, history and physical examinations were performed and blood samples were collected between days 3 and 8 of a spontaneous bleeding episode in the PCOS group and during normal menses of controls. Plasma kisspeptin, serum leptin, and serum RBP4 levels were measured using specific commercial assays. RESULTS: Kisspeptin, leptin, and RBP4 levels were significantly higher in the PCOS group than in controls. Kisspeptin and RBP4 levels were significantly higher among obese PCOS patients than controls. Leptin levels were higher among obese PCOS patients than non-obese PCOS patients or controls. Kisspeptin and leptin levels of PCOS patients were significantly correlated with RBP4 levels. When only obese PCOS patients were analyzed, kisspeptin levels correlated with only the free androgen index. CONCLUSIONS: These findings suggest that kisspeptin, leptin, and RBP4 are associated with metabolic disturbances in women with PCOS.


Subject(s)
Kisspeptins/blood , Leptin/blood , Obesity/metabolism , Polycystic Ovary Syndrome/metabolism , Retinol-Binding Proteins, Plasma/metabolism , Adolescent , Adult , Blood Glucose/metabolism , Body Mass Index , Female , Gonadal Steroid Hormones/blood , Humans , Insulin/blood , Obesity/complications , Polycystic Ovary Syndrome/complications , Young Adult
3.
Microvasc Res ; 83(2): 237-42, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22230112

ABSTRACT

The aim of this study is to evaluate the expression of vascular endothelial growth factor (VEGF) and its soluble receptor (sFlt-1) in peritoneal fluid (PF), peritoneal endometriotic lesions and eutopic endometrial tissues of patients with endometriosis. Peritoneal fluid, peritoneal endometriotic lesions and eutopic endometrial samples from patients with endometriosis, and peritoneal fluid, peritoneal tissue and endometrial samples from patients without endometriosis were obtained during an operative laparoscopy. The mean PF concentrations of VEGF and sFlt-1 were significantly higher in patients with endometriosis than in the controls. In the peritoneal tissue, the expressions of VEGF and sFlt-1 were significantly higher, where the expression of sFlt-1 in endometrium was significantly lower in patients with endometriosis. These findings indicate that not only abnormal expressions of angiogenic factors, but also aberrant expressions of antiangiogenic factors in the peritoneal and endometrial environment seem to be involved in the pathogenesis of endometriosis.


Subject(s)
Ascitic Fluid/chemistry , Endometriosis/metabolism , Endometrium/chemistry , Peritoneum/chemistry , Vascular Endothelial Growth Factor A/analysis , Vascular Endothelial Growth Factor Receptor-1/analysis , Adult , Case-Control Studies , Endometriosis/genetics , Female , Humans , Middle Aged , RNA, Messenger/analysis , Republic of Korea , Up-Regulation , Vascular Endothelial Growth Factor A/genetics , Vascular Endothelial Growth Factor Receptor-1/genetics , Young Adult
4.
Hum Reprod ; 27(2): 515-22, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22158084

ABSTRACT

BACKGROUND: Recently, proteomic technologies have demonstrated that several proteins are differently expressed in various body fluids of patients with endometriosis compared with those without this condition. The aim of this study was to investigate proteins secreted in urine of patients with endometriosis using proteomic techniques in order to identify potential markers for the clinical diagnosis of endometriosis. METHODS: Urine samples were collected from women undergoing laparoscopy for different indications including pelvic masses, pelvic pain, suspicious endometriosis, infertility and diagnostic evaluation. Proteomic techniques and mass spectrometry were used to identify proteins secreted in the urine of the patients with and without endometriosis and quantification of identified protein was performed using western blot and specific commercial sandwich enzyme-linked immunosorbent assays (ELISA). RESULTS: Twenty-two protein spots were differentially expressed in the urine of patients with and without endometriosis, one of which was identified as urinary vitamin D-binding protein (VDBP). ELISA quantification of urinary VDBP corrected for creatinine expression (VDBP-Cr) revealed that urinary VDBP-Cr was significantly greater in patients with endometriosis than in those without (111.96 ± 74.59 versus 69.90 ± 43.76 ng/mg Cr, P = 0.001). VDBP-Cr had limited value as a diagnostic marker for endometriosis (Sensitivity 58%, Specificity 76%). When combined with serum CA-125 levels (the product of serum CA-125 and urinary VDBP-Cr), it did not significantly increase the diagnostic power of serum CA-125 alone. CONCLUSIONS: Urinary VDBP levels are elevated in patients with endometriosis. They have limited value as a potential diagnostic biomarker for endometriosis but suggest it would be worthwhile to investigate other urinary proteins for this purpose.


Subject(s)
Endometriosis/urine , Up-Regulation , Vitamin D-Binding Protein/urine , Adult , Biomarkers/urine , Biomarkers, Tumor/urine , DNA-Binding Proteins/urine , Female , Humans , Middle Aged , Phosphopyruvate Hydratase/urine , Prealbumin/urine , Protein Disulfide-Isomerases/urine , Protein Subunits/urine , Sensitivity and Specificity , Tumor Suppressor Proteins/urine , Young Adult , alpha 1-Antitrypsin/urine
5.
Neuro Oncol ; 13(2): 195-202, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21075779

ABSTRACT

Pseudoprogression is a major diagnostic dilemma in current treatment protocols for malignant gliomas that involve concurrent chemoradiotherapy. We hypothesized that methylation-specific multiplex ligation probe amplification (MS-MLPA), an assay that permits semiquantitative evaluation of promoter methylation, may be used to diagnose pseudoprogression based on the quantification of the methylation status of the O(6)-methylguanine DNA methyltransferase (MGMT) promoter. We examined the methylation ratio of the MGMT promoter with MS-MLPA in 48 samples from glioblastoma patients. The results were compared with those from methylation-specific polymerase chain reaction (MSP), and protein levels were confirmed by immunohistochemical staining. We then evaluated the correlation between those molecular signatures and clinical outcomes. With regard to radiological progression after chemoradiotherapy, the diagnostic accuracy of the MS-MLPA method was 80% (using a cut-off value of 0.2). These results are better than those obtained with MSP (diagnostic accuracy of 68%). Combining the MS-MLPA and MSP methods resulted in a diagnostic accuracy of 93% for the identification of pseudoprogression among patients to whom these results were coherent. These results demonstrate that MS-MLPA is a useful method to predict radiological progression vs pseudoprogression in glioblastoma patients and that the interpretation of these results in combination with MSP results will provide good practical guidelines for clinical decision making in glioblastoma treatment.


Subject(s)
DNA Methylation , Glioblastoma/genetics , Glioblastoma/pathology , Nucleic Acid Amplification Techniques/statistics & numerical data , O(6)-Methylguanine-DNA Methyltransferase/genetics , Promoter Regions, Genetic/genetics , Adult , Aged , Antineoplastic Agents, Alkylating/therapeutic use , Brain Neoplasms/genetics , Brain Neoplasms/pathology , Brain Neoplasms/therapy , Dacarbazine/analogs & derivatives , Dacarbazine/therapeutic use , Disease Progression , Female , Glioblastoma/therapy , Humans , Immunoenzyme Techniques , Male , Middle Aged , Molecular Probe Techniques , Polymerase Chain Reaction , Radiotherapy Dosage , Survival Rate , Temozolomide , Treatment Outcome
6.
Mol Med Rep ; 2(5): 725-32, 2009.
Article in English | MEDLINE | ID: mdl-21475892

ABSTRACT

Lignans isolated from Schisandria chinensis have been prescribed as anti-cancer and anti-hepatitis treatments in Chinese medicine. To investigate the applications of lignans isolated from Schisandria chinensis in hepatic carcinoma therapy, their apoptotic ability was screened using a cell proliferation assay. Compared to the other lignans, gomisin N induced high apoptotic levels in hepatic carcinoma. Cell morphology and flow cytometric analysis demonstrated that this lignan induced cell death at high concentrations, but did not induce any changes at low concentrations. In addition, the expression levels of Bcl-2 and Bax proteins, which are involved in the apoptotic pathway, were markedly increased in only the 320 µM-treated group compared to the vehicle and other concentration groups, while the expression level of p53 protein remained unchanged in this group. These results suggest that gomisin N is an anti-cancer drug candidate capable of inhibiting the proliferation and inducing the apoptosis of human hepatic carcinomas.

7.
Int J Mol Med ; 21(2): 169-79, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18204783

ABSTRACT

Selenoprotein is associated with a variety of serious diseases, including infectious diseases, neurodegenerative disorders, cancer and cardiovascular disease. The aim of this study was to produce a new transgenic (Tg) rat expressing human selenoprotein M (SelM) in order to examine the protective function of the antioxidant status in vivo. To achieve this, a new lineage of Tg rats was produced by the microinjection of pCMV/GFP-hSelM constructs into a fertilized rat egg. Several conclusions can be drawn based on the results of the present study. The human SelM gene was successfully expressed at both the transcription and protein levels in the CMV/GFP-hSelM Tg rats. This Tg rat showed a different enzyme activity for the antioxidant protein in the various tissues examined. In response to the 2,2'-azobiz(2-amidinopropane) dihydrochloride (AAPH) injection, the Tg rats showed a lower level of antioxidant and H2O2 concentration as the activity of the antioxidant enzyme was maintained at a higher level in the Tg rats than in the non-Tg rats. Also, the neutrophil-to-lymphocyte ratio was significantly increased in this Tg rat, even though the level of corticosterone remained unchanged in both genotypes. Thus, the results of this study demonstrated that the CMV/GFP-hSelM Tg rat can serve as an animal model for the maintenance of a high level of antioxidant status and can be used to study the biological function of selenoprotein in infectious diseases, cardiovascular disease and cancer.


Subject(s)
Antioxidants/metabolism , Gene Expression , Glutathione Peroxidase/metabolism , Hydrogen Peroxide/metabolism , Leukocytes/cytology , Selenoproteins/genetics , Superoxide Dismutase/metabolism , Animals , Animals, Genetically Modified , Corticosterone/metabolism , Cytomegalovirus , Disease Models, Animal , Erythrocytes/enzymology , Female , Gene Expression Profiling , Gene Expression Regulation , Genetic Vectors , Green Fluorescent Proteins/metabolism , Humans , Hydrogen Peroxide/blood , Organ Specificity , Rats , Rats, Sprague-Dawley , Selenoproteins/metabolism
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