Research on the Impact of TRAIL on Apoptosis of SKOV3 Cell Line Ovarian Tumor Xenografts in Nude Mice
Huang Qin
Abstract
Huang Qin
Abstract
Objective To investigate the effects of Tumor necrosis factor-related apoptosis-inducing ligand(TRAIL) on the expression of Cysteine/aspartic acid specific protease-3(Caspase-3) in SKOV3 ovarian tumor cells and its relationship with the apoptosis of the ovarian tumor xenografts in nude mice.Methods Twenty-four nude mice with SKOV3 cell line ovarian tumor were randomly divided into four groups with 6 in each group.TRAIL(10 μg/kg) was given to the mice in the TRAIL group;DDP(3 μg/kg) was given to the mice in the DDP group;TRAIL(10 μg/kg) and DDP(3 μg/kg) were given to the mice in the TRAIL+DDP group;and 0.5 mL of saline solution was give to the mice in the control group.The expression of Caspase-3 was detected with immunohistochemistry.The apoptosis index(AI) of cells was determined by Terminal deoxynucleotidyl transferase mediated-dUTP nick end labeling(TUNEL).Results The expression of Caspase-3 in the TRAIL group(171.67±14.38),DDP group(172.50±14.75),and TRAIL+DDP group(230.00±40.99) was significantly higher than that in the control group(135.83±16.25)(P0.05).The apoptosis index for the control group,TRAIL group,DDP group and TRAIL+DDP group was 16.67±5.43,33.17±8.42,24.33±4.59,and 40.50±6.16,respectively.The apoptosis index for the TRAIL group and the TRAIL+DDP group was significantly higher than that in the control group and the DDP group(P0.05).Conclusion Soluble TRAIL has an effect on enhancing the expression of Caspase-3 in implanted tumor in nude mice.TRAIL protein can inhibit the growth of SKOV3 cells in nude mice by inducing cell apoptosis.
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Objective To investigate the effects of Tumor necrosis factor-related apoptosis-inducing ligand(TRAIL) on the expression of Cysteine/aspartic acid specific protease-3(Caspase-3) in SKOV3 ovarian tumor cells and its relationship with the apoptosis of the ovarian tumor xenografts in nude mice.Methods Twenty-four nude mice with SKOV3 cell line ovarian tumor were randomly divided into four groups with 6 in each group.TRAIL(10 μg/kg) was given to the mice in the TRAIL group;DDP(3 μg/kg) was given to the mice in the DDP group;TRAIL(10 μg/kg) and DDP(3 μg/kg) were given to the mice in the TRAIL+DDP group;and 0.5 mL of saline solution was give to the mice in the control group.The expression of Caspase-3 was detected with immunohistochemistry.The apoptosis index(AI) of cells was determined by Terminal deoxynucleotidyl transferase mediated-dUTP nick end labeling(TUNEL).Results The expression of Caspase-3 in the TRAIL group(171.67±14.38),DDP group(172.50±14.75),and TRAIL+DDP group(230.00±40.99) was significantly higher than that in the control group(135.83±16.25)(P0.05).The apoptosis index for the control group,TRAIL group,DDP group and TRAIL+DDP group was 16.67±5.43,33.17±8.42,24.33±4.59,and 40.50±6.16,respectively.The apoptosis index for the TRAIL group and the TRAIL+DDP group was significantly higher than that in the control group and the DDP group(P0.05).Conclusion Soluble TRAIL has an effect on enhancing the expression of Caspase-3 in implanted tumor in nude mice.TRAIL protein can inhibit the growth of SKOV3 cells in nude mice by inducing cell apoptosis.
Key concepts: TUNEL assay, Apoptosis, Medicine, Terminal deoxynucleotidyl transferase, Immunohistochemistry, Necrosis, Fas ligand, Andrology