Application of ezh2 inhibitor compound in preparation of medicament for treating ocular melanoma
A melanoma and compound technology, applied in the medical field, can solve the problems of choroidal melanoma and conjunctival melanoma, the curative effect and mechanism of action are unclear, and there are no reports of application, so as to reduce the rate of enucleation, improve the effectiveness of treatment, and improve visual acuity. prognostic effect
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Embodiment 1
[0018] Immunofluorescence experiment
[0019] Experimental materials: choroidal melanoma tissue chip (Me1004a), purchased from Xi'an Aili Biotechnology Co., Ltd.; H3K27me3 antibody and secondary antibody, purchased from Abcam (Abcam (Shanghai) Trading Co., Ltd.).
[0020] Place the tissue chip in a wet box, and spread PBS on the tissue chip. The diluted H3K27me3 antibody was centrifuged at 13500g for 2min at 4°C. Aspirate the PBS buffer on the glass slide at one end of the tissue chip, and add the antibody from the other end, cover with a humidification box, and incubate at room temperature for 1 h. Wash slides with PBS 3 times (5min / time), add new PBS buffer from one end of the slice, and absorb old buffer from the other end. The diluted secondary antibody was centrifuged at 13500g for 2min at 4°C. Add the secondary antibody on the tissue chip, incubate for 1 h at room temperature in a humidified box, and wash the slides 3 times with PBS (5 min / time). The coverslip was co...
Embodiment 2
[0022] Plate colony formation assay
[0023] Experimental materials: Human choroidal melanoma OCM1, OM431 cells, human conjunctival melanoma CRMM1, CM2005.1 cells, 37°C, 5% CO 2 Conventional culture, the medium is DMEM (Gibco) with 10% fetal bovine serum (FBS); GSK503, GSK343, EPZ005687, EPZ-6438 were purchased from MedChemExpress (MCE China); six-well plates were purchased from Thermo Fisher (Thermo Fisher, USA) ; Crystal violet was purchased from Sangong Company (Sangong China);
[0024] OCM1, OM431, CRMM1, and CM2005.1 were cultured to a density of 70%-80%, and the growth state was good. When the refractive index was high, they were digested and centrifuged, and resuspended with 10% FBS DMEM. For cell counting, 1000 cells / well were spread on a six-well plate, and each well of the six-well plate contained 2 ml of 10% DMEM culture medium. After 2 weeks, stain with crystal violet, wash 2 times with PBS, and take pictures to count the number of cell clones. The results are as...
Embodiment 3
[0026] Cell plate clone proliferation assay
[0027] Experimental materials: CCK8 was purchased from Japan Tongren Chemical Co., Ltd.
[0028] OCM1 and CM2005.1 cells were as described above, retinal pigment epithelial cells ARPE-19 and melanocytes PIG-1 were used as normal controls. OCM1, CM2005.1 cells were seeded in 96-well plates, 2000 cells per well, 100ul culture medium, ARPE19 and PIG-1 cells were 4000 cells per well, 37°C, 5% CO 2 Cultivate, add 10ulCCK8 at 0h, 24h, 48h, and 72h respectively, continue to incubate at 37°C for 4h, measure the absorbance value at OD450nm on the machine, and the results are as follows image 3 shown. EZH2 inhibitor can significantly inhibit the proliferation of retinoblastoma, and the inhibitory effect is enhanced with the increase of concentration. The drug at the same concentration has little toxicity to normal cells.
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