Application of cGAMP in prevention of colorectal cancer hepatic metastases
A technology for colorectal cancer and liver metastases, applied in the field of biomedicine, can solve the problem that liver metastases cannot be radically resected
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Embodiment 1
[0011] Example 1 : cGAMP preparation of
[0012] cGAMP (cyclized-GMP-AMP) is catalyzed by cyclized cGMP-AMP dinucleotide synthetase (cGAS) under the conditions of activation after binding to DNA according to the literature method. The purity is above 98%. (Pingwei Li, et al., Immunity, 2013, 39(6), 1019-1031.)
Embodiment 2
[0013] Example 2 : cGAMP (cyclization -GMP-AMP ) anti-tumor effect was tested by tumor-bearing mouse model cGAMP Inhibitory effect on liver metastasis of colorectal cancer in animals.
[0014] Test drug
[0015] Name: cGAMP
[0016] Appearance: white powder
[0017] Vehicle: normal saline.
[0018] Preparation method: Prepare the solution with the required concentration with physiological saline solution before use.
[0019] Test drug concentration: 1 mg / ml, 2 mg / ml.
[0020] animal
[0021] Species, strains, gender, body weight, source, certificate of conformity
[0022] C57 mice, male, weighing 16-18 g, 6-8 weeks old, were purchased from Shanghai Slack Experimental Animal Co., Ltd. [Experimental animal quality certificate number: SCXK (Shanghai) 2007-0005].
[0023] Feeding conditions
[0024] All mice were free to forage for food and drink water, and were kept at room temperature (23±2)°C in the Experimental Animal Center of a Military Medical Un...
Embodiment 3
[0053] Example 3 : Flow cytometry test of mouse dendritic cells ( DC cell) activation efficiency
[0054] See Example 2 for mouse breeding and colorectal cancer metastasis model modeling. Anti-CD40, CD80, CD86, MHC II, isotype control antibodies and other flow antibodies were purchased from eBiosciences, CD11c+ antibody magnetic beads were purchased from Miltenyi Biotech, and flow cytometers were purchased from BD. The mice were sacrificed 14 days after the administration, and the spleens of the mice were taken, ground and crushed, and the cells were filtered through a 40 um pore membrane. Centrifuge at 1000rpm for 10 minutes to separate the immune cells in the spleen, lyse the erythrocytes with erythrocyte lysate until the erythrocytes are completely dissolved, and then centrifuge at 1000rpm for 10 minutes to separate the unlysed immune cells. Separate DC cells with CD11c+ antibody magnetic beads, add anti-CD40, CD80, CD86, MHC II FAC antibodies (diluted with FACS b...
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