Genomic medicine for inhabiting lung cancer transfer and pulmonary metastatic tumor
A technology for lung cancer metastasis and drugs, which is applied in gene therapy, anti-tumor drugs, drug combinations, etc., can solve the problems such as the inability to play the target organ tumor treatment purpose well, and the low concentration of anti-tumor angiogenesis factors.
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Embodiment 1
[0073] Preparation of rAAV2 / 2-eGFP
[0074] The composition of the expression frame of the eGFP expression plasmid is as follows: the promoter is CMV enhancer / chicken β-actin promoter, eGFPcDNA, polyA, WPRE. The two ends of the expression box are AAV2ITR.
[0075] Prepare recombinant virus by calcium phosphate-free helper virus multi-plasmid method: co-transfect 293 cells with eGFP expression plasmid, AV helper plasmid, and rAAV2 helper plasmid, harvest cells after 60-72 hours, and use sodium deoxycholate (0.5%) Cleavage with benzonase (30u / m1), centrifugation (3000g 30min) to remove cell debris, cesium chloride gradient centrifugation to obtain the recombinant virus rAAV2 / 2-eGFP, and chromatographic purification.
Embodiment 2
[0077] rAAV2 / 1-eGFP, rAAV2 / 3-eGFP, rAAV2 / 4-eGFP, rAAV2 / 5-eGFP, rAAV2 / 6-eGFP, rAAV2 / 7-eGFP, rAAV2 / 8-eGFP, rAAV2 / 9-eGFP, rAAV2 / Preparation of 10-eGFP and rAAV2 / 11-eGFP
[0078] Referring to the steps in Example 1, the rAAV2 helper plasmids were replaced with rAAV1, rAAV3, rAAV4, rAAV5, rAAV6, rAAV7, rAAV8, rAAV9, rAAV10, and rAAV11, and the remaining operations were the same as in Example 1 to obtain 11 different serotypes of rAAV viruses.
Embodiment 3
[0080] Screening for lung-tropic rAAV serotypes
[0081] The titers of the various serotypes of rAAV obtained in Example 2 were determined by Real-PCR method. The primers used were designed according to the sequence of WPRE, respectively WPRE-F (5'-TGGCGTGGTGTGCACTGT) and WPRE-R (5'-GTTCCGCCGTGGCAATAG).
[0082] LLC cells or HLEC cells were seeded into 24-well plates and cultured overnight. Add the various serotype rAAV viruses that contain embodiment 2 and obtain respectively (MOI 10 4 ) serum-free medium, after incubation for 5 hours, it was replaced with normal medium. After 72 hours, the cells were observed with a fluorescent microscope, and the cells were sorted with a flow cytometer, and the transduction efficiency was calculated (n=3).
[0083] Table 3 Transduction efficiency of different serotypes of rAAV to LLC cells or HLEC cells
[0084] rAAV serotype
[0085] It can be seen that the transduction efficiency of various serotypes of rAAV to LLC cells or ...
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