- 2
- 0
- 约6.74千字
- 约 20页
- 2019-02-16 发布于福建
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Background Background Tyrosine kinase inhibitors (TKIs) belong to a new class of anticancer drugs. TKIs including lapatinib, erlotinib and sunitinib, have been shown to overcome ABC transporters-mediated MDR in cancer cells. Apatinib (YN968D1) is an oral small-molecule TKI that targets VEGFR-2, RET, c-Kit and c-Src tyrosine kinases. It is conceivable that apatinib may inhibit functions of ABC transporters by binding to their ATP-binding sites. Cytotoxicity of apatinib alone in all experimental cell lines Potentiation of antitumor effects of paclitaxel by apatinib in a xenograft model of KBv
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