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1.
Journal of Experimental Hematology ; (6): 1162-1166, 2018.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-689512

ABSTRACT

<p><b>OBJECTIVE</b>To detect the expression level of cyclooxygenase-1(COX-1) and cyclooxygenase-2(COX-2) in the platelet of iron deficiency anemia(IDA)women at childbearing age and to explore its correlation with the different indexes of anemia and platelets.</p><p><b>METHODS</b>Forty female IDA patients at childbearing age and 35 healthy controls were enrolled in this study. The Flow cytometry was used to detect the expression of platelet COX-1 and COX-2,the platelet aggregation function as examined by turbidimetric method,and the levels of serum ferritin were analyzed by electrochemical luminescence method,the leval of serum iron was determined by ELISA,and the correlation of different indexes was analyzed.</p><p><b>RESULTS</b>Compared with healthy controls,the levels of platelet COX-1 and COX-2 were significantly lower in female IDA patients at Childbearing age(P<0.05),but platelet count(Plt),mean platelet volume(MPV) and platelet aggregation rate(PAgT)were not statistically different between the 2 groups(P > 0.05). The expression level of platelet COX-1 positively correlated with those of Hb(r =0.623,P<0.01),serum iron(r =0.321,P<0.05) and HCT(r=0.305,P<0.05). but the platelet COX-2 expression did not corelate with these indexs.</p><p><b>CONCLUSION</b>The expression of platelet COX-1 and COX-2 in female IDA patients at Childbearing age markedly decrease,and the expression level of platelet COX-1 closely relates with the severity of anemia,that possesses reference value for clinical diagnosis of female IDA patients at Childbearing age..</p>


Subject(s)
Female , Humans , Anemia, Iron-Deficiency , Blood Platelets , Cyclooxygenase 1 , Cyclooxygenase 2 , Ferritins , Platelet Aggregation , Platelet Count
2.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-289947

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of short hairpin RNA (shRNA) targeting N-acetylglucosaminyltransferase V (GnT-V) on the proliferation of prostate cancer PC-3 cells.</p><p><b>METHODS</b>Lipofectamine 2000 was used to transfect the recombinant plasmids carrying the shRNA targeting GnT-V gene into PC-3 cells. Semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) was used to measure the mRNA expression of GnT-V, and CCK-8 assay was used to measure the cell proliferation after the transfection.</p><p><b>RESULTS</b>The recombinant plasmids were successfully transfected into PC-3 cells, resulting in a reduction of GnT-V mRNA expression by 73%. The proliferation of PC-3 cells was significantly inhibited after the transfection.</p><p><b>CONCLUSION</b>The shRNA targeting GnT-V gene can reduce the expression of GnT-V mRNA and inhibit the proliferation of PC-3 cells in vitro.</p>


Subject(s)
Humans , Male , Cell Line, Tumor , Cell Proliferation , N-Acetylglucosaminyltransferases , Genetics , Prostatic Neoplasms , Genetics , Pathology , RNA Interference , RNA, Small Interfering , Genetics , Transfection
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