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1.
Chinese Medical Journal ; (24): 670-673, 2015.
Article in English | WPRIM | ID: wpr-357939

ABSTRACT

<p><b>BACKGROUND</b>Non-small cell lung cancer (NSCLC) is a prolific and high-mortality disease with few effective treatments. Although the detection and surgical techniques for NSCLC continue to advance, the survival rate for the patients with NSCLC remains poor. Enhanced predictive biomarkers such as microRNAs (miRNAs) are needed at the time of diagnosis to better tailor therapies for patients. This study focused on the expression of miR-1280 in NSCLC tissues and distal normal tissues in order to explore the association between miR-1280 expression and NSCLC.</p><p><b>METHODS</b>A total of 72 newly diagnosed primary NSCLC patients were enrolled in this study. Quantitative real-time polymerase chain reaction (PCR) was performed to identify the expression level of miR-1280 in the NSCLC tissues and distal normal tissues of these patients.</p><p><b>RESULTS</b>The miR-1280 expression was significantly higher in the NSCLC tissues (0.084 ± 0.099) than distal normal tissues (0.014 ± 0.015, P = 0.009). In 54 patients (75%), the miR-1280 expression in the NSCLC tissues was upregulated (2-ΔΔct > 2), and no case showed a downregulation of miR-1280 expression.</p><p><b>CONCLUSIONS</b>The expression level of miR-1280 could be regarded as a biomarker for NSCLC.</p>


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Carcinoma, Non-Small-Cell Lung , Genetics , Gene Expression Regulation, Neoplastic , In Vitro Techniques , Lung Neoplasms , Genetics , MicroRNAs , Genetics , Real-Time Polymerase Chain Reaction , Up-Regulation
2.
Chinese Journal of Experimental and Clinical Virology ; (6): 138-140, 2013.
Article in Chinese | WPRIM | ID: wpr-318081

ABSTRACT

<p><b>OBJECTIVE</b>Of this study was to prepare high sensitivity and high specificity of highly pathogenic H5N1 subtype avian influenza virus NS1 protein antibody and a preliminary assessment of its potency.</p><p><b>METHODS</b>Construct pET-28a (+) recombinant vector containing the H5N1 subtype of avian influenza virus NS1 sequences of E. coli BL21 (DE3), induced expression of NS1 protein, NS1 recombinant protein was obtained by Ni-NTA column purified by affinity chromatography, and SDS-PAGE and Western Blot analysis. Purified protein antigen to immunize New Zealand white rabbits, obtained rabbit anti-NS1 serum, affinity-purified polyclonal antibodies. Using ELISA and Western Blot analysis of purified antibody titer and specificity.</p><p><b>RESULTS</b>NS1 fusion protein was highly expressed in a purity of greater than 90%, with the fusion protein was used to immunize New Zealand white rabbits anti-NS1 polyclonal antibody titer of 1:80 000, and specific recognition of the H5N1 subtype of avian influenza virus NS1 protein.</p><p><b>CONCLUSIONS</b>NS1 polyclonal antibodies to NS1 recombinant protein purified antigen, with better potency and specificity, and to prepare the conditions for the development of the H5N1 subtype of avian influenza virus detection kit.</p>


Subject(s)
Animals , Rabbits , Antibodies, Viral , Allergy and Immunology , Escherichia coli , Genetics , Influenza A Virus, H5N1 Subtype , Allergy and Immunology , Recombinant Fusion Proteins , Allergy and Immunology , Viral Nonstructural Proteins , Genetics , Allergy and Immunology
3.
Chinese Journal of Experimental and Clinical Virology ; (6): 224-227, 2013.
Article in Chinese | WPRIM | ID: wpr-318057

ABSTRACT

<p><b>OBJECTIVE</b>A novel multiplex real-time RT-PCR kit was developed to detect EV71, CoxA16 and other human enteroviruses simultaneously with an internal amplification control to avoids false negatives, which used for hand, foot and mouth disease in the clinical diagnosis and epidemiological surveillance.</p><p><b>METHODS</b>Design specific primers and probes of EV71, CA16, other intestinal virus and internal amplification control, improve the extraction method of virus nucleic acid. Optimization the detection system of real-time quantitative PCR. Research the products of the accuracy, stability, precision, amplification efficiency and detection of linear range.</p><p><b>RESULTS</b>The primers and probes had high spicificity. The Viral RNA extraction effect of this Kit is as same as that of QIAamp Viral RNA mini Kit (QIAGEN company), but less reagent cost. The optimal concentrations of primers and probes are 0.2 micromol/L for all the upstream and downstream primers, 0.06 micromol/L for probes of other human enteroviruse, 0.08 micromol/L for probes of EV71 and CA16 respectively. The kit has good stability, accuracy and precision. The amplification efficiencies of EV71, CoxA16 and other human enteroviruses are 106% ,101% and 105% and the detection of linear range is from 10(9) copies/microl-10(2) copies/microl.</p><p><b>CONCLUSION</b>The novel multiplex real-time RT-PCR kit for detecting EV71, CoxA16 and other human enteroviruses simultaneously with an internal amplification control has good stability, accuracy, precision and amplification efficiencies. So it has great value in clinical application.</p>


Subject(s)
Humans , Enterovirus , Reagent Kits, Diagnostic , Real-Time Polymerase Chain Reaction , Methods
4.
Chinese Medical Journal ; (24): 2045-2050, 2011.
Article in English | WPRIM | ID: wpr-319149

ABSTRACT

<p><b>BACKGROUND</b>Progranulin is a newly discovered 88-kDa glycoprotein originally purified from the highly tumorigenic mouse teratoma-derived cell line PC. Its expression is closely correlated with the development and metastasis of several cancers. However, no immunohistochemical evidence currently exists to correlate progranulin expression with clinicopathologic features in breast carcinoma biopsies, and the role of progranulin as a new marker of metastatic risk and prognosis in breast cancer has not yet been studied. The aim of this study was to investigate the clinicopathologic and prognostic implications of progranulin expression in breast carcinoma and its correlation with tumor angiogenesis.</p><p><b>METHODS</b>Progranulin expression was determined immunohistochemically in 183 surgical specimens from patients with breast cancer and 20 tissue samples from breast fibroadenomas. The tumor angiogenesis-related biomarker, vascular endothelial growth factor was assayed and microvessel density was assessed by counting vascular endothelial cells in tumor tissues labeled with endoglin antibody. The relationship between progranulin expression and the clinicopathologic data were analyzed.</p><p><b>RESULTS</b>Progranulin proteins were overexpressed in breast cancer. The level of progranulin expression was significantly correlated with tumor size (P = 0.004), lymph node metastasis (P < 0.001) and TNM staging (P < 0.001). High progranulin expression was associated with higher tumor angiogenesis, reflected by increased vascular endothelial growth factor expression (P < 0.001) and higher microvessel density (P = 0.002).</p><p><b>CONCLUSION</b>Progranulin may be a valuable marker for assessing the metastasis and prognosis of breast cancer, and could provide the basis for new combination regimens with antiangiogenic activity.</p>


Subject(s)
Female , Humans , Middle Aged , Antigens, CD , Metabolism , Breast Neoplasms , Metabolism , Endoglin , Immunohistochemistry , In Vitro Techniques , Intercellular Signaling Peptides and Proteins , Metabolism , Receptors, Cell Surface , Metabolism , Vascular Endothelial Growth Factor A , Metabolism
5.
Chinese Medical Journal ; (24): 1338-1344, 2010.
Article in English | WPRIM | ID: wpr-352563

ABSTRACT

<p><b>BACKGROUND</b>Interleukin 10 (IL-10) is an important cytokine with anti-inflammatory, anti-immune and anti-fibrotic functions. This study aimed at evaluating the relationship between allele polymorphisms in the IL-10 promoter region and hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.</p><p><b>METHODS</b>The odds ratios (ORs) of IL-10 allele distributions in patients with HBV or HCV infection were analyzed against healthy controls. All the relevant studies in PubMed were identified, and poor qualified studies were excluded. The meta-analysis software REVMAN 4.2 was applied for investigating heterogeneity among individual studies and summarizing all the studies. The publication bias was also evaluated.</p><p><b>RESULTS</b>This study demonstrated a significant association between the IL-10-592 A/C polymorphism and HBV infection in the Asian population under the overall effect size of allele A versus C. In our subgroup meta-analysis, we found a significant association of IL-10-592 A/C polymorphism to HCV infection susceptibility in Asian populations, although sensitivity analysis showed that the combined result was not associated with the worldwide population. Other IL-10 allele polymorphisms were not associated with HBV or HCV infection.</p><p><b>CONCLUSION</b>IL-10-592 A/C allele might be a risk factor for HBV or HCV in Asians but not in Europeans.</p>


Subject(s)
Humans , Alleles , Genetic Predisposition to Disease , Genetics , Hepatitis B , Epidemiology , Genetics , Hepatitis C , Epidemiology , Genetics , Interleukin-10 , Genetics , Polymorphism, Genetic , Genetics , Promoter Regions, Genetic , Genetics
6.
Chinese Medical Journal ; (24): 734-738, 2010.
Article in English | WPRIM | ID: wpr-242580

ABSTRACT

<p><b>BACKGROUND</b>Embryonic stem (ES) cells poss unlimited self-renewal capacity and the ability to differentiate into cell of all three germ layers in vitro. Induced differentiation of ES cells to neural lineage cells has great potential in basic study of neurogenesis and regeneration therapy of neurodegenerative diseases. Histone deacetylase (HDAC) inhibitors enhance histone acetylation so that globularly activate gene expression and may initiate multilineage differentiation. In this study, we aimed to develop a method to induce the differentiation of ES cells to neural cells combining HDAC inhibition and neural cell selection.</p><p><b>METHODS</b>In this study, we used HDAC inhibitor sodium butyrate (NaB) to induce the differentiation of mouse embryonic stem cells to neural cells through monolayer culture. After differentiation initiation by histone deacetylase inhibitor sodium butyrate, neural cells were induced and selected with a serum free culture system.</p><p><b>RESULTS</b>Homogeneous neurons without glial cells demonstrated by molecular marker expression were differentiated with the method. The resultant neurons were excitable.</p><p><b>CONCLUSION</b>The method combined differentiation induction effect of HDAC inhibitors and selective culture system to derive neural cells from ES cells, and implied the involvement of epigenetic regulation in neural differentiation.</p>


Subject(s)
Animals , Mice , Butyrates , Pharmacology , Cell Adhesion , Cell Cycle , Cell Differentiation , Cells, Cultured , Embryonic Stem Cells , Cell Biology , Fibroblast Growth Factor 2 , Pharmacology , Histone Deacetylase Inhibitors , Pharmacology , Neurons , Cell Biology , Physiology
7.
Chinese Journal of Experimental and Clinical Virology ; (6): 30-32, 2006.
Article in Chinese | WPRIM | ID: wpr-305532

ABSTRACT

<p><b>BACKGROUND</b>To understand the significance of detection of serum sialic acid (SA) and Epstein-Barr virus VCA-IgA (EBV-CA-IgA) in diagnosis and monitoring radiotherapy effectiveness of nasopharyngeal carcinoma (NPC) patients.</p><p><b>METHODS</b>Serum SA and EBV-CA-IgA were detected in 65 cases with NPC before radiotherapy and one months after radiotherapy and 21 cases one year after radiotherapy for NPC with local recurrence and/or distant metastasis. Healthy persons and patients with benign lesions of head and neck were also enrolled as control group.</p><p><b>RESULTS</b>SA and EBV-CA-IgA of NPC patients before radiotherapy were significantly higher than those in control group (P<0.01). The sensitivity of combination of SA and EBV-CA-IgA (96.9%) was higher than those determined alone (P<0.05). The SA level of NPC patients after radiotherapy and without recurrence after radiotherapy was reduced significantly compared to the NPC patients before radiotherapy (P<0.01). The SA level of NPC patients with recurrence was significantly higher than that in NPC patients without recurrence (P<0.01), whereas the positive rate of EBV-CA-IgA changed little.</p><p><b>CONCLUSION</b>Dynamic detection of serum SA may be a valuable technique for diagnosis and monitoring radiotherapy effectiveness in NPC patients. The combined determination of the two indexes can raise the positive rate of patients with NPC.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Antigens, Viral , Allergy and Immunology , Capsid Proteins , Allergy and Immunology , Follow-Up Studies , Herpesvirus 4, Human , Allergy and Immunology , Immunoglobulin A , Blood , N-Acetylneuraminic Acid , Blood , Nasopharyngeal Neoplasms , Blood , Radiotherapy , Virology , Treatment Outcome
8.
Chinese Journal of Biotechnology ; (12): 171-176, 2005.
Article in Chinese | WPRIM | ID: wpr-249930

ABSTRACT

Orthotopic liver transplantation has proven to be effective in the treatment of a variety of life-threatening liver diseases, however, the limitations of donated organs available and long-term immunosuppression provided an impetus for developing alternative therapies. Cell replacement strategies have been one major effective approach for overcoming the obstacles of organ transplantation in recent years. The exogenous cells should be able to proliferate and differentiate into mature hepatic cells after grafting. Use of mature hepatocytes is also hampered by limited tissue source and inability to proliferate and maintain the function for a long term in vitro. Embryonic stem cells are immortal and pluripotent and may provide a novel cell source for potential cell therapy. This review summarizes the mechanisms of controlling early liver development and hepatic differentiation of visceral endoderm in embryoid bodies, and provides an overview of diverse differentiation systems in vitro and in vivo that were applied to hepatic research in recent years. Several studies have demonstrated that ES cell-derived hepatocytes can incorporate into liver tissue and function in vivo , but a few of them have shown complete restoration of liver function after transplantation into mice with liver diseases. Further studies should be made to exploit efficient methods and clinical applications of hepatocytes derived from ES cells in the future. In addition to clinical transplantation for treatment of liver diseases, ES cells can provide a valuable tool for drug discovery applications and study on of molecular basis of hepatic differentiation.


Subject(s)
Animals , Humans , Cell Differentiation , Physiology , Cells, Cultured , Embryonic Stem Cells , Cell Biology , Transplantation , Hepatocytes , Cell Biology , Liver Diseases , Therapeutics
9.
Cancer Research and Clinic ; (6)1999.
Article in Chinese | WPRIM | ID: wpr-676405

ABSTRACT

0.05).Conclusion MK mRNA overexpresses in the breast cancer tissues.It might be considered to be a reference indicator for deter- mining the angiogenesis and invasion of breast carcinoma.

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