Mouse subcutaneous tumor xenografts were established as described in a previous report15. After the tumor volumes reached ~200 mm3, the mice were divided into two groups: the tumor growth monitoring and prolonged survival evaluation groups. Each group was randomized into 4 subgroups and administered the following treatments: vehicle, 30 mg/kg/day sorafenib, 3 mg/kg/day prazosin, or both treatments. For tumor growth monitoring, tumor dimensions and volumes were measured and recorded, after which the mice were euthanized15. The endpoint for prolonged survival was set as either death or a tumor volume reaching 2000 mm3, following which the mice were euthanized33. Prolonged survival was estimated using the Kaplan–Meier method33. The tumor burden of all the mice in the two independent sets of experiments followed the restriction of an average tumor diameter of no more than 20 mm (volume < 4000 mm3). All animal studies followed the guidelines of the Institutional Laboratory Animal Care and Use Committee of National Taiwan University.
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