Construction method of nasopharyngeal carcinoma tumor model and application
A construction method and technology of nasopharyngeal carcinoma, applied in the field of nasopharyngeal carcinoma tumor model construction, can solve the difficulty of nasopharyngeal carcinoma tumor model construction and other problems
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[0054] In some embodiments, the method for preparing a nasopharyngeal carcinoma cell line capable of expressing luciferase comprises: infecting C666-1 cells with a lentivirus carrying a luciferase gene.
[0055] In some embodiments, the step of obtaining the nasopharyngeal carcinoma cell line suspension expressing luciferase comprises: adding the cell concentration to (0.8~1.2)×10 6 The luciferase-expressing nasopharyngeal carcinoma cell culture fluid per ml was mixed with Corning Matrigel. Experiments have proved that using Corning Matrigel to prepare nasopharyngeal carcinoma cell line suspension for subcutaneous tumor formation can speed up the growth of subcutaneous tumors and save experimental time.
[0056] In some embodiments, the tissue adhesive can be selected from 3M Vetbond.
[0057] In some embodiments, the step of taking subcutaneously cultured nasopharyngeal carcinoma tumors and cutting them into tumor tissue pieces includes: taking out the nasopharyngeal carcino...
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[0065] Embodiment: the method specific steps of described model making are as follows:
[0066] Step S1: Establishing a nasopharyngeal carcinoma cell line with stable high expression of luciferase, specifically:
[0067] Step S1a: C666-1 cells in good growth state were cultured, and the day before virus infection, 2×10 5 C666-1 cells were cultured on 6-well culture plates, and the C666-1 cells in logarithmic growth phase were infected with luciferase (luciferase / Luc) gene lentivirus, added serum-free DMEM culture medium, and placed at 5% CO 2 , Cultivate in a 37°C incubator for 6 hours, then replace with normal medium, and observe the transfection effect after 48 hours;
[0068] Step S1b: Monoclonal screening was performed on the infected cells with a culture medium containing 3 μg / ml puromycin, and C666-1-Luc cells stably and highly expressing luciferase were selected.
[0069] Step S1c: After the purified luciferase-infected human nasopharyngeal carcinoma cell line C666-1...
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