The inhibition of fragile histidine triad gene on the proliferation and tumorigenicity of mucoepidermoid carcinoma cells / 华西口腔医学杂志
West China Journal of Stomatology
;
(6): 252-255, 2008.
Article
in Chinese
| WPRIM
| ID: wpr-296663
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the suppression effect of exogenous fragile histidine triad (FHIT) gene on biological property of MEC-1 cells.</p><p><b>METHODS</b>In order to study the FHIT function in MEC-1 cells, wild-type FHIT gene was transferred into mucoepidermoid carcinoma MEC-1 cells. The proliferation and kinetics, cell cycle, clonal forming rate, and apoptosis of MEC-1 cells, before and after FHIT gene transfection in vitro, and tumor loci formed on mice after injection of transferred MEC-1 cells in vivo were observed by immunochemical staining, flow cytometry analysis, and so on.</p><p><b>RESULTS</b>It can be seen that exogenous FHIT gene transfer could significantly inhibit the proliferation and reduce the kinetics of MEC-1 cells in vitro, prolong DT from (21.03+/-0.41) h to (26.86+/-0.71) h, and also keep less cells in cell cycle phase S, whilst more cells in phase G1, Additionally, the exogenous FHIT was found to be able to remarkably suppress MEC-1 cells of forming tumor loci in nude mice by lessen tumor weight, and promote higher differentiation of MEC-1 cells to be mucous cells.</p><p><b>CONCLUSION</b>Exogenous FHIT gene could suppress the proliferation, tumorigenicity and improve the differentiation of MEC-1 cells, in vitro and in vivo.</p>
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Transfection
/
Cell Cycle
/
Apoptosis
/
Carcinoma, Mucoepidermoid
/
Acid Anhydride Hydrolases
/
Cell Line, Tumor
/
Histidine
/
Mice, Nude
/
Neoplasm Proteins
Limits:
Animals
/
Humans
Language:
Chinese
Journal:
West China Journal of Stomatology
Year:
2008
Type:
Article
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