Synthesized MyD88 inhibitor retards hepatic carcinoma growth in tumor-bearing BALB/c mice

来源 :22nd Asia Pacific Cancer Conference(第22届亚太抗癌大会) | 被引量 : 0次 | 上传用户:sm2998
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Objective: To elevate expression of MyD88 was found in HCC patients.Tumor growth and metastasis may be attributed to such increased expression.Methods: For the in vitro study, a synthesized MyD88 inhibitor was incubated with murine hepatocyte carcinoma H22 cells for2, 4, 16, 24, and 30 h separately.The working concentrations of the synthesized MyD88 inhibitor were set to 20, 40, and 80μM.Cell proliferation and cell viability were estimated by BrdU assay and Alamar Blue analysis.For the in vivo study, 2x10s H22 cells were pre-treated with 40 μM MyD88 inhibitor for4 h and subcutaneously injected into the BALB/c mice.The tumor growth and the tumor size of BALB/c mice generated by MyD88 inhibitor-treated H22 cells were compared with those generated by untreated H22 cells.To estimate the antitumor effects of MyD88 inhibitor, tumor formation was established in a BALB/c mouse by H22 cells and then basally injected with MyD88 inhibitor.Tumor-bearing mice without MyD88 inhibitor treatment were used as controls.
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