2007Chinese Journal of Public HealthRequires access

Effects of cyclooxygenase-2 on proliferation and apoptosis in HepG2 cells

Xiaoyun Zeng

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Abstract

Objective To examine the effects of a selective inhibitor of cox-2,celecoxib on growth and apoptosis in HepG2 cells.Methods HepG2 cells were treated with various concentrations of celecoxib.Cell growth was measured by MTT,apoptosis was detected by DNA fragmentation assay,and cox-2 activity was measured by RIA;Expression of caspase3 protein in HepG2 cells was determined by western blot,and caspase-3 activity was measured using colorimetric assay.Results After HepG2 cells were treated with different concentrations of celecoxib(12.5,25,50μmol/L),celecoxib could significantly suppress the growth of HepG2 cells respectively compared with the control group(P0.01),and celecoxib-treated HepG2 cells produced a distinct oligosomal ladder,the characteristics of cells undergoing apoptosis;Meanwhile,The caspas-3 expression and activity of celecoxib treated HepG2 cells were increased respectively as compared with the control groups(P0.01).Furthermore,the level of cox-2 activity was reduced in celecoxib-treated HepG2 cells respectively compared with the control group(P0.01).Conclusion Celecoxib could inhibit the proliferation and increase apoptosis in HepG2 cells by cox-2 and caspase3 pathways.

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Objective To examine the effects of a selective inhibitor of cox-2,celecoxib on growth and apoptosis in HepG2 cells.Methods HepG2 cells were treated with various concentrations of celecoxib.Cell growth was measured by MTT,apoptosis was detected by DNA fragmentation assay,and cox-2 activity was measured by RIA;Expression of caspase3 protein in HepG2 cells was determined by western blot,and caspase-3 activity was measured using colorimetric assay.Results After HepG2 cells were treated with different concentrations of celecoxib(12.5,25,50μmol/L),celecoxib could significantly suppress the growth of HepG2 cells respectively compared with the control group(P0.01),and celecoxib-treated HepG2 cells produced a distinct oligosomal ladder,the characteristics of cells undergoing apoptosis;Meanwhile,The caspas-3 expression and activity of celecoxib treated HepG2 cells were increased respectively as compared with the control groups(P0.01).Furthermore,the level of cox-2 activity was reduced in celecoxib-treated HepG2 cells respectively compared with the control group(P0.01).Conclusion Celecoxib could inhibit the proliferation and increase apoptosis in HepG2 cells by cox-2 and caspase3 pathways.

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Available abstract

Objective To examine the effects of a selective inhibitor of cox-2,celecoxib on growth and apoptosis in HepG2 cells.Methods HepG2 cells were treated with various concentrations of celecoxib.Cell growth was measured by MTT,apoptosis was detected by DNA fragmentation assay,and cox-2 activity was measured by RIA;Expression of caspase3 protein in HepG2 cells was determined by western blot,and caspase-3 activity was measured using colorimetric assay.Results After HepG2 cells were treated with different concentrations of celecoxib(12.5,25,50μmol/L),celecoxib could significantly suppress the growth of HepG2 cells respectively compared with the control group(P0.01),and celecoxib-treated HepG2 cells produced a distinct oligosomal ladder,the characteristics of cells undergoing apoptosis;Meanwhile,The caspas-3 expression and activity of celecoxib treated HepG2 cells were increased respectively as compared with the control groups(P0.01).Furthermore,the level of cox-2 activity was reduced in celecoxib-treated HepG2 cells respectively compared with the control group(P0.01).Conclusion Celecoxib could inhibit the proliferation and increase apoptosis in HepG2 cells by cox-2 and caspase3 pathways.

Key concepts: Celecoxib, Apoptosis, DNA fragmentation, Western blot, Cell growth, Fragmentation (computing), Cyclooxygenase, Chemistry

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