Application of AKR1C1 protein
A protein and lung cancer technology, applied in the application field of AKR1C1 protein, to achieve accurate diagnosis of lung cancer, improve accuracy, and increase in vitro metastasis and invasion capabilities
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Embodiment 1
[0024] Female nude mice aged 4-6 weeks were used for experiments. The non-small cell lung cancer cell line NCI-H1299 stably and highly expressing AKR1C1 group and the control group were collected by EDTA digestion, washed twice with the culture medium, and injected into the tail vein of nude mice. Each nude mouse was injected with 2 million cells in a volume of 200 μL. After 60 days, they were sacrificed by cervical dislocation and dissected to observe organ metastasis and take pictures. like figure 1 As shown, in the group with high expression of AKR1C1, the liver metastasis in nude mice was significantly higher than that in the control group.
Embodiment 2
[0026] The subcultured lung cancer cells NCI-H1650 and NCI-H1299 were transfected with the AKR1C1 gene (AKR1C1 group) respectively, and a blank control (pcmv6 group) was set. After 24 hours of transfection, the in vitro invasion ability of transfected cells was detected by Transwell method. like figure 2 As shown, after overexpressing the AKR1C1 gene, the in vitro invasion ability of lung cancer cells NCI-H1650 and NCI-H1299 was significantly increased.
Embodiment 3
[0028] In subcultured lung cancer cells A549 and PC-9, RNA interference was used to inhibit the expression of AKR1C1 (AKR1C1 group), and a blank control (NC group) was set. After 24 hours of interference, the in vitro invasion ability of transfected cells was detected by Transwell method. like image 3 As shown, after the interference inhibited the expression of AKR1C1, the in vitro invasion ability of lung cancer cells A549 and PC-9 was significantly reduced.
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