Establishing method and applications of cell model capable of simulating lung cancer occurrence mechanism
A cell model and mechanism technology, applied in the field of cell medicine, can solve the problems of complex pathogenesis of lung cancer and single inducing factor, etc.
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Embodiment 1
[0044] Example 1: Conditional exploration and model construction of the effect of spherical SNPs on BPDE-infected BEAS-2B cells co-cultured with THP-1 cells
[0045] 1Exploration of optimal concentration
[0046] The medium used for culturing BEAS-2B and THP-1 cells is LHC-9 medium containing 10% FBS, and the medium is replaced every 2-3 days.
[0047] 1.1 Exploration steps
[0048] ⑴ Set the complete medium as the blank group, and the cells without any poison treatment as the control group, and set 3 parallel holes for each dose experimental group;
[0049] ⑵Adjust the concentration of BEAS-2B cells or THP-1 cells to 1×10 5 Pcs / ml, evenly seeded in 96-well plate, 200ul per well, after the cells grow adherently for 24 hours, discard the original culture medium;
[0050] ⑶ The concentrations of BPDE added are 0, 200nmol / ml, 400nmol / ml, 800nmol / ml and 1.2umol / ml; the concentrations of spherical SNPS are 0, 1.5625μg / ml, 3.125μg / ml, 6.25μg / ml, 12.5μg / ml and 25μg / ml;
[0051] ⑷ Discard the cu...
Embodiment 2
[0085] Example 2: Comparison of cytokine expression in serum of established cell model and actual lung cancer patients
[0086] 1 Cytokine detection in cell model
[0087] 1.1 Grouping
[0088] The experiment is divided into two groups: the control group is BEAS-2B cells + 800 nmol / L BPDE stimulation + THP-1; the experimental group is BEAS-2B cells + 800 nmol / L BPDE stimulation + THP-1 + 12.5 μg / ml spherical SNPs .
[0089] 1.2 Experimental steps
[0090] (1) Suspension chip experiment
[0091] The two groups of cells were cultured for 24 hours and 48 hours to detect the culture supernatant. According to the instruction of the suspension chip kit (Bio-Plex), the expression level of each cytokine was detected.
[0092] (2) Realtime-PCR experiment
[0093] The two groups of cells were cultured for 24 hours and 48 hours to detect the culture supernatant. RNA was extracted from the two groups of cells for RT-qPCR detection, and the BEAS-2B and THP-1 cells infected with BPDE and BPDE-SNPs we...
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