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1.
Chinese Journal of Preventive Medicine ; (12): 515-521, 2008.
Article in Chinese | WPRIM | ID: wpr-352452

ABSTRACT

<p><b>OBJECTIVE</b>To study the differential gene expression profiling of rats exposed to silica using the normal rats as control.</p><p><b>METHODS</b>Animal models were established using intratracheal injection of the lung and 22 107 genes were screened in the differential expression profiling of silicosis by using oligonucleotide bead array. Differential expression profiling data were analyzed by using DAVID bioinformation software.</p><p><b>RESULTS</b>Totally 1567 differentially expressed genes were identified in lungs of silica exposed rats including 765 up-regulated genes and 802 down-regulated genes as compared to the normal controls. Among 406 annotated genes in KEGG pathways, 204 genes and 11 pathways were up-regulated as well as 202 genes and 3 pathways were down-regulated in silica exposed rats.</p><p><b>CONCLUSION</b>All 1567 genes are involved in the formation of silicosis. The differential gene expression profile of silicosis describes the general changes in the gene expressions in silicosis at transcriptional level. Further analysis of the identified genes might help reveal the molecular mechanism of pulmonary fibrosis induced by silica.</p>


Subject(s)
Animals , Male , Rats , Disease Models, Animal , Gene Expression Profiling , Lung , Metabolism , Pathology , Oligonucleotide Array Sequence Analysis , Pulmonary Fibrosis , Genetics , Metabolism , Rats, Wistar , Silicosis , Genetics , Metabolism , Pathology
2.
Chinese Journal of Preventive Medicine ; (12): 522-526, 2008.
Article in Chinese | WPRIM | ID: wpr-352451

ABSTRACT

<p><b>OBJECTIVE</b>To seek differentially expressed serum proteins in recovered SARS patients complicating avascular necrosis of femoral head (AVNFH).</p><p><b>METHODS</b>2-DE and MALDI-TOF MS were used to study the comparative serum proteomics among female SARS AVNFH group, female SARS non-AVNFH group and female healthy group. ELISA method was used to detect serum amyloid P component in individual serum; specificity and sensitivity of serum amyloid P component were analyzed.</p><p><b>RESULTS</b>Average protein points on 2-DE of 3 groups were 632 +/- 28, 671 +/- 55, 688 +/- 42 respectively, and the matching rate of protein points was ranged from 85% to 95%; eighteen differentially expressed proteins were discovered including transthyretin, serpin peptidase inhibitor, alpha-1-antitrypsin precursor, serum amyloid P components, etc. Compared to healthy group and SARS non-AVNFH group, transthyretin, C4B3, fibrinogen gamma, apolipoprotein L, apolipoprotein A-IV precursor, albumin and prealbumin showed lower expression, inversely serpin peptidase inhibitor, alpha-1-antitrypsin precursor and serum amyloid P components showed higher expression in serum in the SARS AVNFH necrosis group. The serum amyloid P component in 3 groups were 0.54 +/- 0.30 ng/ml, 0.83 +/- 0.39 ng/ml, 1.21 +/- 0.29 ng/ml respectively. The areas under the ROC curve on serum amyloid P component was 0.854, the specificity was 77.8% and the sensitivity was 85.2%.</p><p><b>CONCLUSION</b>There were differentially expressed serum proteins in three groups. Serum amyloid P components might be one of the potential biomarkers in serum of recovered SARS patients complicating avascular necrosis of femoral head.</p>


Subject(s)
Adult , Female , Humans , Blood Proteins , Case-Control Studies , Electrophoresis, Gel, Two-Dimensional , Femur Head Necrosis , Blood , Proteomics , Severe Acute Respiratory Syndrome , Blood , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
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