Dual-therapy with αvβ3-targeted Sn2 lipase-labile fumagillin-prodrug nanoparticles and zoledronic acid in the Vx2 rabbit tumor model

αvβ3 靶向 Sn2 脂肪酶不稳定的烟曲霉素前药纳米粒子和唑来膦酸在 Vx2 兔肿瘤模型中的双重治疗

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作者:Alison K Esser, Anne H Schmieder, Michael H Ross, Jingyu Xiang, Xinming Su, Grace Cui, Huiying Zhang, Xiaoxia Yang, John S Allen, Todd Williams, Samuel A Wickline, Dipanjan Pan, Gregory M Lanza, Katherine N Weilbaecher

From the clinical editor

Although anti-angiogenesis is one of the treatment modalities in the fight against cancer, many cancers become resistant to VEGF pathway inhibitors. In this article, the authors investigated the use of dual therapy using fumagillin, integrin-targeted lipid-encapsulated nanoparticles (αvβ3- Fum-PD NP) and zoledronic acid (ZA), in both in-vitro and in-vivo experiments. This combination approach may provide an insight to the design of future drugs against cancers.

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