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We investigated the impact of PTGER4 on endometrial tumour development in vivo using a nude mouse model.
The ability of hBD-3 to chemoattract host macrophages in vivo using a nude mouse model and analysis of hBD-3 on monocytic cell migration in vitro, applying a cross-desensitization strategy of CCR2 and its pharmacological inhibitor (RS102895), respectively, was also carried out.
We finally evaluated the antitumor effects of ANT2 shRNA in vivo using a nude mouse tumor xenograft model.
Using a nude mouse model, CDK11p58 inhibited the growth and density of microvessels of the transplanted tumor.
When we repeated the various experiments using a nude mouse intracranial tumor model, we were unable to obtain stable results.
Using a nude mouse orthotopic xenograft model, we assessed the in vivo metastatic ability of MCF-7-14-EGFP cells.
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In vivo animal experiments, using a nude mice xenograft model, demonstrated that an increased amount of mPEG-FA-NPs or FA-NPs were accumulated in the tumor tissue relative to the mPEG-NPs or NPs alone.
We also examined the effect of triptolide on CCA growth using a nude mice model of CCA derived from the highly malignant CCA cell line HuCCT1.
In our studies using a nude mice Jurkat xenograft model, tumor volumes were reduced compared with controls after BITC treatment, indicating an antileukemia activity of this compound.
On the other hand, Lu et al., using a nude mice model, showed that fluorescent mesoporous silica nanoparticles of 130 nm with 2 nm pores are well tolerated via intraperitoneal and intravenous administration [100].
We used a nude mouse xenograft model to determine the effects of COX-2 inhibition in breast cancer.
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