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1.
Journal of Medical Informatics ; (12): 53-58,68, 2017.
Article in Chinese | WPRIM | ID: wpr-669156

ABSTRACT

The paper begins with the ontology construction requirements based on ontology reuse and transformation of existing resources,combines the current situations of study on technical progress and tools for ontology construction at home and abroad,and conducts code development of tools for ontology construction and function realization based on WebProtege class library.In the process of realization,pay attention to the interactive mode of combination of automatic tool processing and manual review,and collect specific sample data to verify the feasibility and usability of applying the developed tools for ontology construction.

2.
Basic & Clinical Medicine ; (12): 1596-1600, 2017.
Article in Chinese | WPRIM | ID: wpr-665101

ABSTRACT

Objective To estimate outcome and prognostic risk factors of special type endometrial cancer .Methods Clinic data was collected in Peking Union Medical College Hospital during 2005-2010 .SPSS software was used to analyze data .Logistic regression analysis was used to analyze prognostic risk factors respectively .Results Medium follow up time of total 48 endometrial serous carcinoma , clear cell carcinoma and carcinosarcoma patients was 70.5 months.Most of patients could be diagnosed at early time ( FIGO stage Ⅰand stage Ⅱwere 66.7%among all pa-tients) .The main treatment was operation and followed by chemo-therapy and radio-therapy.66.7%of patients ac-cepted chemo-therapy after operation , and 41.7%of patients accepted radio-therapy .The outcome of advanced pa-tients was poor.30.8%stage Ⅲrelapsed and died in 3 years.The recurrence rate and mortality of stage Ⅳwere all 100%.The recurrence rate of advance endometrial serous carcinoma was 80%, which was much higher than the other two.FIGO stage and lymphatic metastasis were the main prognostic risk factors .Conclusions Special type of endometric cancer has a poor prognosis and lymphatic metastasis is main reason to explain the prognosis .

3.
Chinese Journal of Cardiology ; (12): 1056-1061, 2012.
Article in Chinese | WPRIM | ID: wpr-292042

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effects of interleukin-8 monoclonal antibody on smooth muscle cell proliferation and balloon inflation-induced abdominal aorta stenosis in rabbits.</p><p><b>METHODS</b>Thirty-six New Zealand white rabbits were randomly assigned to balloon inflation group (group A, n = 12), interleukin-8 monoclonal antibody pre-treated rabbits (2 mg/kg for 3 days before balloon inflation, group B, n = 12) and sham-operated control group (group C, n = 12). Peripheral blood was collected before experiment and at 4 h, 1, 3, 7, 14, and 28 days post balloon inflation or sham operation and the levels of IL-8 were measured by enzyme linked immunosorbent assay (ELISA). The ratio of positive and negative masculine cells in the high power microscopic field was determined in proliferating cell nuclear antigen (PCNA) stained slide. Histopathologic examination was performed in abdominal aorta and luminal area, intima and tunica media area were measured.</p><p><b>RESULTS</b>Plasma interleukin-8 began to rise at 4 h and peaked at 1 day and remained increased up to 28 days after balloon inflation in rabbits of group A, plasma interleukin-8 level in group A was significantly higher than in group B and C at 4 h and thereafter post operation. The ratio of positive and negative masculine cells was significantly increased in group A compared to group C and was significantly lower in group B than in group A. Abdominal aorta stenosis, luminal area, intima and tunica media area were significantly reduced in group B than in group A. Correlation analysis indicated that there were positive relations between plasma IL-8 level and intima thickness, area of intima and tunica media, respectively (r = 0.894, 0.783, 0.801, 0.912, all P < 0.01).</p><p><b>CONCLUSIONS</b>Plasma IL-8 level is increased in this abdominal aorta stenosis model and is positively correlated to the severity of abdominal aorta stenosis. IL-8 monoclonal antibody could significantly reduce abdominal aorta stenosis in this abdominal aorta stenosis model.</p>


Subject(s)
Animals , Rabbits , Antibodies, Monoclonal , Pharmacology , Therapeutic Uses , Aorta, Abdominal , Pathology , Aortic Coarctation , Drug Therapy , Pathology , Cell Proliferation , Interleukin-8 , Allergy and Immunology , Muscle, Smooth, Vascular , Cell Biology , Myocytes, Smooth Muscle
4.
Chinese Medical Journal ; (24): 2403-2409, 2008.
Article in English | WPRIM | ID: wpr-265926

ABSTRACT

<p><b>BACKGROUND</b>The necrosis of a large number of myocardial cells after acute myocardial infarction (AMI) results in a decrease of cardiac function and ventricle remodeling. Stem cell transplantation could improve cardiac function after AMI, but the involving mechanisms have not been completely understood. The present study aimed to investigate the effects of transplantation of autologous bone marrow mononuclear cells (BM-MNC) and mesenchymal stem cells (MSCs) via the coronary artery on the ventricle remodeling after AMI as well as the mechanisms of the effects of transplantation of different stem cells on ventricle remodeling.</p><p><b>METHODS</b>A total of 36 male pigs were enrolled in this study, which were divided into 4 groups: control group, simple infarct model group, BM-MNC transplantation group, and MSCs transplantation group. At 90 minutes when a miniature porcine model with AMI was established, transplantation of autologous BM-MNC ((4.7 +/- 1.7) x 10(7)) and MSCs ((6.2 +/- 1.6) x 10(5)) was performed in the coronary artery via a catheter. Ultrasound, electron microscope, immunohistochemical examination and real time reverse transcriptase-polymerase chain reaction were used respectively to observe cardiac functions, counts of blood vessels of cardiac muscle, cardiac muscle nuclear factor (NF)-kappaB, myocardial cell apoptosis, and the expression of the mRNA of vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) in cardiac muscles. Multivariate Logistic regression was used to analyze the correlation factors of left ventricular end-diastolic diameter (EDD).</p><p><b>RESULTS</b>The number of blood vessels in the infarct zone and around its border in the BM-MNC transplantation group was more than those in the infarct model group and MSCs group (P = 0.0001) and there was less myocardial cell apoptosis in the stem cell transplantation group than that in the infarct model group (all P < 0.01). The positive rate of NF-kappaB in the stem cell transplantation group was lower than that in the infarct model group (P = 0.001). The gene expression of VEGF in the infarct border zone of the BM-MNC group was higher than that in the MSCs group (P = 0.0001). The gene expression of bFGF in the infarct border zone in the MSCs transplantation group was higher than that in the infarct model group and the BM-MNC group (P = 0.0001). Left ventricular ejection fraction was inversely proportional to the apoptotic rate of myocardial cells and cardiac muscle NF-kappaB but positively correlated with the number of blood vessels and the expression of VEGF and bFGF in the infarct zone and infarct border zone. The Multivariate Logistic regression analysis on the factors influencing the left ventricular end-diastolic diameter after stem cell transplantation showed that the expression of VEGF mRNA in the cardiac muscles in the infarct zone, the number of apoptotic myocardial cells and the expression of NF-kappaB in the infarct border zone were independent factors for predicting the inhibitory effect on the dilation of left ventricular EDD after stem cell transplantation.</p><p><b>CONCLUSIONS</b>Transplantation of autologous BM-MNC and MSCs in pigs can improve the condition of left ventricular remodeling and recover the cardiac functions after AMI. The improvement of cardiac functions is related to the increase of blood vessels, the increased expression of VEGF and bFGF, the reduction of myocardial cell apoptosis, and the decrease of NF-kappaB level in cardiac muscle tissues after stem cell transplantation.</p>


Subject(s)
Animals , Male , Bone Marrow Transplantation , Methods , Disease Models, Animal , Heart Function Tests , Myocardial Infarction , General Surgery , Stem Cell Transplantation , Methods , Swine , Treatment Outcome , Ventricular Remodeling
5.
Chinese Journal of Biotechnology ; (12): 391-396, 2006.
Article in Chinese | WPRIM | ID: wpr-286278

ABSTRACT

A transfer plasmid vector pUC18-US10-VP2 was first constructed by inserting the gene of the enhancer green fluorescent protein(eGFP) fused to the VP2 gene of very virulent Infectious bursal disease virus (IBDV) JS strain into the US10 fragment of the Marek's disease virus (MDV) CV1988/Rispens. The recombinant virus, designated as rMDV, was developed by co-transfecting CEF with the transfer plasmid vector and simultaneously infecting with the CVI988/Rispens virus. The PCR and IFA results indicated that the rMDV is stable after 31 passages. Chickens vaccinated with rMDV were protected from challenge with 100LD50 of IBDV JS. The protection ratio of the chickens vaccinated with the 1000PFU, 2000PFU, 5000PFU of the rMDV were 50%, 60%, and 80% respectively. It is interesting that the average histopathology BF lesion scores of chicken group immunized with 5000PFU of rMDV by one-time vaccination was close to that of chicken group vaccinated with IBDV live vaccine NF8 strain for twice (2.0/1.5). There is no difference in protection between the groups (P > 0.05) but significent difference between groups immunized with 5000 PFU of rMDV and with normal MDV. This demonstrated that rMDV expressing VP2 fusion protein was effective vaccine against IBDV in SPF chickens.


Subject(s)
Animals , Birnaviridae Infections , Chickens , Genetic Vectors , Green Fluorescent Proteins , Genetics , Infectious bursal disease virus , Genetics , Allergy and Immunology , Mardivirus , Genetics , Metabolism , Recombinant Fusion Proteins , Genetics , Allergy and Immunology , Recombination, Genetic , Transfection , Vaccination , Vaccines, DNA , Genetics , Allergy and Immunology , Viral Structural Proteins , Genetics , Allergy and Immunology , Viral Vaccines , Genetics , Allergy and Immunology
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