CYP3A5 protein, encoding gene and recombinant vector and application thereof in preparing drugs for resisting tumor recurrence or metastasis
A technology of encoding genes and recombinant vectors, applied in the field of biomedicine, can solve the problems of few research results of CYP3A5, achieve the effect of inhibiting migration and invasion ability, liver cancer recurrence and metastasis prevention
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Embodiment 1
[0035] This embodiment provides CYP3A5 protein, the coding gene of CYP3A5 protein, the expression cassette containing the coding gene, the recombinant vector and the recombinant bacteria.
[0036] 1. Construction of a vector carrying the gene encoding the CYP3A5 protein
[0037] The eukaryotic expression plasmid pcDNA3.1-CYP3A5 carrying the gene encoding CYP3A5 protein and the lentiviral expression plasmid lenti-CYP3A5-GFP carrying the gene encoding CYP3A5 protein were both constructed by Shanghai Jikai Gene Chemical Technology Co., Ltd. Wherein, the amino acid sequence of the CYP3A5 protein is shown in SEQ ID NO.1, and the nucleotide sequence of the gene encoding the CYP3A5 protein is shown in SEQ ID NO.2.
Embodiment 2
[0039] This embodiment provides viral vectors, such as lentiviral vectors, and recombinant cells containing genes encoding CYP3A5 protein.
[0040] 1. Vector transformation to construct SMMC-7721 and HCC-LM3 two stable cell lines overexpressing CYP3A5 protein
[0041]The SMMC-7721 and HCC-LM3 cells in good growth state were transferred to 6-well plates respectively, and when the cell confluence rate was 60%-70%, the serum-free DMEM medium containing the above-mentioned lenti-CYP3A5-GFP was added (MOI=20 ), continue culturing for 8-9 hours, and then replace with fresh serum-containing DMEM medium. After culturing for another 6-10 days, the cells with green fluorescence were sorted by flow cytometry, which were stable cell lines with CYP3A5 overexpression. Two stable cell lines overexpressing CYP3A5 protein, SMMC-7721 and HCC-LM3, were obtained respectively.
Embodiment 3
[0043] This embodiment provides the application of the above CYP3A5 protein in inhibiting the recurrence or metastasis of tumor cells such as liver cancer cells.
[0044] 1. In vitro experiments to detect the effect of overexpression of CYP3A5 protein on the migration ability and invasion ability of liver cancer cells
[0045] The SMMC-7721 and HCC-LM3 cells transformed with the above-mentioned lentiviral vectors expressing CYP3A5 protein were used as the treatment group; the SMMC-7721 and HCC-LM3 cells transformed with the lentiviral vectors expressing the GFP protein were used as the control group. The effect of overexpression of CYP3A5 protein on the metastasis and invasion ability of liver cancer cells SMMC-7721 and HCC-LM3 was detected.
[0046] (1) Transwell method was used to detect the migration ability of liver cancer cells in the treatment group and the control group. The specific steps are as follows.
[0047] Rehydrate the inner chamber of Matrigel precoated trans...
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