Drug-resistant glioblastoma cell line of primary temozolomide and bevacizumab, construction method and application of cell line
A technology for glioblastoma and bevacizumab, applied in the direction of microorganism-based methods, animal cells, tumor/cancer cells, etc., can solve problems such as not being able to guide the application well, and achieve stable and stable properties genetic effect
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[0046] Example 1 Construction of primary drug-resistant glioblastoma cell lines
[0047] 1. Experimental method
[0048] Surgical specimens obtained from patients with human glioblastoma were surgically obtained, and the dispersed tumor cells were obtained by enzymatic digestion. They were placed in culture flasks containing medium, and continuously subcultured to 50 generations to obtain glioblastoma with stable passage in vitro. cell line. The specific implementation steps are as follows:
[0049] 1. Processing of Surgically Obtained Tumor Tissue
[0050] Put the tissue samples obtained from the operation into the culture medium containing penicillin and streptomycin, and place them in a liquid nitrogen tank; bring them into the laboratory for processing within 30 minutes; wash the tissue blocks repeatedly in the ultra-clean workbench to remove Blood vessels and blood clots; use ophthalmic scissors to cut the tissue block into a size of about 3-5mm 3 Small pieces of smal...
experiment example 1
[0059] Experimental example 1 Biological characteristics identification experiment of primary drug-resistant glioblastoma LC-11 cell line
[0060] 1. Morphological observation
[0061] Place the culture flask of cultured LC-11 cells under an inverted microscope and take pictures under bright field. The cells grow adherently. It can be seen that the tumor cells have various shapes. Most of the cells are spindle-shaped, and some are triangular and polygonal. Loss of contact inhibition between cells, showing malignant growth, with the characteristics of overlapping growth ( Figure 4 ).
[0062] 2. Karyotype analysis
[0063] After the cultured LC-11 cells were placed at 4°C for 12 hours, colchicine was added to make the final concentration 4 μg / ml, and then placed in a 37°C incubator for 10 hours. Cells in the mid-division stage were collected, fixed with a fixative, and then the cell suspension was lowered onto a pre-cooled slide, stained with Giemas staining solution, and t...
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