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1.
Chinese Journal of Experimental and Clinical Virology ; (6): 381-383, 2011.
Article in Chinese | WPRIM | ID: wpr-246233

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the value of plasma ProGRP, CYFRA 21-1 and CEA in patients with lung cancer.</p><p><b>METHODS</b>The levels of plasma ProGRP, CYFRA 21-1 and CEA were detected in 85 healthy control, 49 benign lung diseases and 143 lung neoplasms. The levels of ProGRP in the patients with SCLC was monitored.</p><p><b>RESULTS</b>The level of plasma ProGRP in SCLC (M 179.1 ng/ml) was significantly higher than adenocarcinoma (M 35.3 ng/ml), squamous-cell carcinoma (M 33.3 ng/ml), healthy control (M 35.6 ng/m) and benign lung diseases (M 33.3 ng/m), P < 0.001. The sensitivity and specificity for diagnosing SCLC by ProGRP were 60.6% and 95.0% respectively. In the effective treatment group, ProGRP reduced 45.9%, in the progression group, ProGRP increased 103.1%, P < 0.05. The level of CEA in the metastatic adenocarcinoma (M 10.22 ng/ml) was significantly higher than non-metastatic adenocarcinoma (M 3.85 ng/ml) and squamous cell carcinoma (M 2.56 ng/ml) (P < 0.01).</p><p><b>CONCLUSION</b>The plasma ProGRP is a good indicator for diagnosing and evaluating cure effect in SCLC; the high expression of CEA is related to the metastatic adenocarcinoma.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Antigens, Neoplasm , Blood , Carcinoembryonic Antigen , Blood , Case-Control Studies , Diagnostic Techniques and Procedures , Gastrin-Releasing Peptide , Blood , Keratin-19 , Blood , Lung Neoplasms , Blood , Diagnosis , Small Cell Lung Carcinoma , Blood , Diagnosis
2.
National Journal of Andrology ; (12): 896-899, 2008.
Article in Chinese | WPRIM | ID: wpr-309753

ABSTRACT

<p><b>OBJECTIVE</b>To compare the incidences of sexual dysfunction induced by mirtazapine and SSRI in the treatment of patients with depression.</p><p><b>METHODS</b>Using key-word retrieval from the compact disks of the Chinese biological medicine (CBM) data base, we analyzed the rates of sexual dysfunction from the published clinical control trials on depression treated with mirtazapine and SSRI by applying the fixed effects model (FEM) of evidence-based medicine (EBM).</p><p><b>RESULTS</b>Among 1108 cases in 14 studies, there were 5 cases of mirtazapine-induced and 106 cases of SSRI-induced sexual dysfunction, accounting for 0.90% and 19.2% respectively, OR = 0.07 (95% CI: 0.04-0.14), Z = 8.03, P < 0.01.</p><p><b>CONCLUSION</b>SSRI is far more likely to induce sexual dysfunction than mirtazapine in the treatment of depression.</p>


Subject(s)
Humans , Male , Antidepressive Agents, Tricyclic , Depressive Disorder , Drug Therapy , Erectile Dysfunction , Mianserin , Selective Serotonin Reuptake Inhibitors
3.
Chinese Journal of Surgery ; (12): 1634-1636, 2007.
Article in Chinese | WPRIM | ID: wpr-338095

ABSTRACT

<p><b>OBJECTIVE</b>To study the inducible expression of hypoxia-inducible factor 1alpha (HIF-1alpha) on the proliferation and invasion property of HepG2 cells under normoxia in vitro.</p><p><b>METHODS</b>Constructed the HepG2(Tet-on-HIF-1alpha) cell line which could induce the expression of HIF-1alpha by doxycycline; Under normoxia in vitro, MTT assay was used to observe the proliferative and adhesive activity of cells, and the invasive activity was determined by transwell cell culture chamber method.</p><p><b>RESULTS</b>Under normoxia, the HIF-1alpha mRNA and protein of HepG2(Tet-on-HIF-1alpha) cells could be induced up to (5.899 +/- 2.176) and (2.179 +/- 0.742) folds by doxycycline (1 microg/ml); There were no difference of A(490 nm) between the Dox(+)and Dox(-) group in experiment detecting the proliferation activity (P > 0.05); But in adhesive experiment, the A(490 nm) of Dox (+) group was 0.662 +/- 0.058, higher than the Dox(-) group 0.526 +/- 0.808 (P = 0.008); The invasive cell number of Dox(+) group was 37.611 +/- 8.424, but in the Dox(-) group, the number was 25.333 +/- 8.117 (P < 0.01).</p><p><b>CONCLUSIONS</b>Under normoxia in vitro, the Tet-on gene regulate system could increase the HIF-1alpha protein by inducing the HIF-1alpha mRNA; HIF-1alpha has no influence with the proliferation activity, but it could enhance the adhesive and invasive properties of HepG2 cells.</p>


Subject(s)
Humans , Blotting, Western , Carcinoma, Hepatocellular , Genetics , Metabolism , Pathology , Cell Adhesion , Cell Line, Tumor , Cell Movement , Cell Proliferation , Cell Survival , Gene Expression Regulation, Neoplastic , Hypoxia-Inducible Factor 1, alpha Subunit , Genetics , Metabolism , Physiology , Liver Neoplasms , Genetics , Metabolism , Pathology , Neoplasm Invasiveness , RNA, Messenger , Genetics , Metabolism , Reverse Transcriptase Polymerase Chain Reaction
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