Radiosensitization ofcelecoxib on human lung adenocarcinoma cell line A549 and inhibition of migration abilityin vitro

2010 
:Objective To investigatethe effects of radiosensitivity enhancement and inhibition of migration ability of humanlung adenocarcinoma cells by celecoxib,a selective cyclooxygenase (COX)-2inhibitor.Methods Human lung adenocarcinoma cells of the line A549 were cultured and theninoculated into six-well plates and randomly divided into 4 groups:control group,celecoxibgroup administered with celecoxib at the subtoxic doses 30 and 50 μmol/L,irradiatedgroup exposed to 0,1,2,4,6,or 8 Gy by linear accelerator,and combined treatment (celecoxib+ irradiation) group.The radiosensitizing effect of celecoxib was assessed by clonogeniccell survival test.The migration ability of the A549 cells was measured by scratch-woundtest and the content of metalloproteinase-2 (MMP-2) in culture supernatant was detectedwith ELISA.Results The sensitization enhancement ratio of the celexib group was increaseddosedependently.The values of D0 ,Dq,SF2 and D0.01 of the celecoxib + irradiation groupwere all significantly lower than those of the irradiated group.Scratch-wound test showedthat the no-scratch area of the celecoxib + irradiation group and celecoxib group were allsignificantly wider than those of the mere irradiation and control groups and there was adose-dependent manner,and the no-scratch area of the celecoxib + irradiation group waswlider than that of the celecoxib group.ELISA showed that the MMP-2 levels in thesupernatant of the celecoxib group and celecoxib + irradiation group were respectivelysignificantly lower than those of the control group and mere irradiated group (t =3.78,5.79、3.15,P < 0.05),however,there was notsignificant difference between the mere irradiation and control groups (t = 2.73,2.38,P> 0.05).ConclusionsCelecoxib enhances concentration-dependently the radiosensitivity of human lung carcinomacell and inhibits the secretion of MMP-2 of the carcinoma cells,thus inhibiting theirmigration ability. Key words: Lungneoplasms;  Radiosensitivity;  Cyclo-oxygenase-2 (COX-2); Metalloproteinase-2 (MMP-2)
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