Application of NSC 23766 in tumor radiotherapy assistance
A technology of NSC23766, 1. NSC23766, applied in NSC23766 in the field of adjuvant tumor radiotherapy, can solve the problems of limited patient prognosis, high local treatment failure rate, cytotoxicity, etc., and achieve the effect of increasing radiotherapy sensitivity
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experiment example 1
[0025] Experimental Example 1 Verification that NSC 23766 inhibits the proliferation activity of LLC cells
[0026] Mouse lung cancer cells LLC were incubated with 10 μM, 50 μM, and 100 μM NSC23766 for 2 h, followed by 0 Gy (non-irradiated), 4 Gy and 8 Gy irradiation treatments, and the proliferation activity of LLC cells was detected by CCK-8 after 24 h. The experimental results showed that: ①Inhibition of Rac1 itself can significantly reduce the proliferation activity of LLC cells; ②50μM and 100μM administration groups can significantly reduce the cell proliferation activity of LLC after different doses of irradiation, that is, the damage effect of sensitized irradiation on LLC cells.
[0027] Such as figure 1 As shown, different doses of Rac1 inhibitor NSC23766 were detected on the proliferation activity of LLC cell line CCK-8. *** represents the corresponding group compared with the PBS control group under the same irradiation dose, P<0.001. The error value adopts mean±S...
experiment example 2
[0028] Experimental Example 2 Verification that NSC 23766 promotes apoptosis of mouse lung cancer cells after irradiation
[0029] Mouse lung cancer cells LLC were incubated with PBS or 100μM NSC23766 for 2h, 0Gy (non-irradiated) or 10Gy irradiated, and 24h later, cell apoptosis was detected by flow cytometry Annexin V / PI method. The experimental results showed that: ①Under the condition of 0Gy without irradiation, there was no significant difference in the apoptosis rate of LLC cells between the administration group and the control group; ②After 10Gy irradiation, the apoptosis rate of each group increased significantly; ③After 10Gy irradiation, the apoptosis rate of the administration group was significantly Higher than the control group (P<0.05). The above results indicated that irradiation induced the apoptosis of mouse lung cancer cells LLC, and NSC 23766 could increase the apoptosis of LLC cells after irradiation, that is, there was a certain sensitization effect on the r...
experiment example 3
[0031] Experimental example 3 Animal experiments
[0032] A total of 33 C57BL / 6 male mice aged 6-8 weeks were selected. After the tumor cells were digested with trypsin containing EDTA, the culture medium was added to resuspend and the cells were counted. Dilute the cell suspension to 4 x 10 7 cells / ml. Medium and Matrigel 1:1, each mouse was injected with 50ul into the right lung through the incision under the right armpit, that is, the number of tumor-bearing cells in the lung of each mouse was 1×10 6 indivual. One week after the lung tumor was loaded, three animals were sacrificed by cervical dislocation, the tumor on the right side of the lung was removed, and the size of the lung tumor was measured by weighing method. The photos and weight of the tumor are as follows: image 3 shown.
[0033] From the second week, the lung tumor-bearing mice were randomly divided into two groups: intraperitoneal injection of PBS group and intraperitoneal injection of 3 mg / kg NSC23766...
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