Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 1 de 1
Filtre
1.
Chinese Journal of Oncology ; (12): 486-489, 2006.
Article Dans Chinois | WPRIM | ID: wpr-236952

Résumé

<p><b>OBJECTIVE</b>To investigate the function and mechanism of 3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole (YC-1) on activity of VEGF and GPI genes in human pancreatic cancer PC-3 cells incubated under hypoxic conditions.</p><p><b>METHODS</b>Human pancreatic cancer PC-3 cells were incubated under hypoxic culture conditions. Immunocytochemical staining was used to detect HIF-1alpha protein expression in hypoxic and normoxic PC-3 cells. Semi-quantitative RT-PCR was used to detect the effect of YC-1 on the expression of VEGF and GPI mRNA and HIF-1alpha protein in PC-3 cells. Effect of YC-1 on the expression of HIF-1alpha protein was examined by Western blotting. MTF assay was used to detect proliferation of hypoxicPC-3 cells.</p><p><b>RESULTS</b>HIF-1alpha expression was mainly located in nuclei in hypoxic PC-3 cells. The mRNA synthesis of VEGF and GPI and the protein expression of HIF-1alpha were significantly decreased in the group treated with the highest concentration of YC-1 (100 micromol/L). Compared to placebo, YC-1 inhibited the proliferation of hypoxic PC-3 cells greatly when it was increased to 100 micromol/L.</p><p><b>CONCLUSION</b>YC-1 inhibited the transcription of VEGF and GPI in hypoxic human pancreatic cancer PC-3 cells. It was induced by down-regulation of HIF-1alpha protein. YC-1 inhibites the proliferation of PC-3 cells exposed to hypoxic conditions.</p>


Sujets)
Humains , Technique de Western , Hypoxie cellulaire , Lignée cellulaire tumorale , Prolifération cellulaire , Activateurs d'enzymes , Pharmacologie , Régulation de l'expression des gènes tumoraux , Glucose 6-phosphate isomerase , Génétique , Métabolisme , Sous-unité alpha du facteur-1 induit par l'hypoxie , Métabolisme , Indazoles , Pharmacologie , Tumeurs du pancréas , Métabolisme , Anatomopathologie , ARN messager , Génétique , Métabolisme , RT-PCR , Transcription génétique , Facteurs de croissance endothéliale vasculaire , Génétique , Métabolisme
SÉLECTION CITATIONS
Détails de la recherche