Composition, culture medium and method for 3D culture of laryngeal cancer tissue
A composition and medium technology, applied in the field of 3D cultured laryngeal cancer tissue composition, can solve the problems of laryngeal cancer cell differences, laryngeal cancer tissue is difficult to culture into organoids, and laryngeal cancer basic and clinical research cannot be carried out, etc. achieve high consistency
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Embodiment 1
[0037]The invention provides a culture medium for 3D culture of laryngeal cancer tissue, comprising: B27 serum-free additive, 0.5×; Wnt3A, 200ng / ml; N-acetylysteine, 1.5mM; EGF, 30ng / mL; Noggin, 150ng / mL; R-spondin 1, 200ng / mL; GSK1838705A, 2nM; FGF10, 40ng / mL; Nicotinamide, 20mM; Y-27632, 2μM; SB202190, 10μM; mL. The solvent was SAGM medium. The preparation method of the medium is as follows: formulating ingredients according to the final concentrations of all components, and then mixing with SAGM medium.
Embodiment 2
[0039] The invention provides a culture medium for 3D culture of laryngeal cancer tissue, comprising: B27 serum-free additive, 2×; Wnt3A, 50ng / ml; N-acetylysteine, 1mM; EGF, 100ng / mL; Noggin , 200ng / mL; R-spondin 1, 1000ng / mL; GSK1838705A, 2nM; FGF10, 10ng / mL; Nicotinamide, 5mM; Y-27632, 20μM; FGF2, 30ng / mL; SB202190, 10μM; . The solvent was SAGM medium. The preparation method of this culture medium is the same as that of Example 1.
Embodiment 3
[0041] The invention provides a culture medium for 3D culture of laryngeal cancer tissue, comprising: B27 serum-free additive, 1×; Wnt3A, 500ng / ml; N-acetylysteine, 0.15mM; EGF, 60ng / mL; Noggin, 50ng / mL; R-spondin 1, 500ng / mL; GSK1838705A, 0.5nM; FGF10, 50ng / mL; Nicotinamide, 10mM; Y-27632, 10μM; mL; trans-retinoic acid: 100 nM; BMP7: 10 ng / mL. The solvent was SAGM medium. The preparation method of this culture medium is the same as that of Example 1.
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