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Re: An epirubicin-conjugated nanocarrier with MRI function to overcome lethal multidrug-resistant bladder cancer

机译:回复:具有核磁共振功能的表柔比星偶联纳米载体可克服致命的多药耐药性膀胱癌

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Multidrug resistance (MDR) presents a major obstacle to curing cancer. Chemotherapy failure can occur through both cell membrane drug resistance (CMDR) and nuclear drug resistance (NDR), and anticancer effectiveness of chemotherapeutie agents is especially reduced by their nuclear export. Here we report an exciting magnetically-targeted nanomedicine formed by conjugation of epirubicin (EPI) to non-toxic and high-magnetization nanocarrier (HMNC). Strikingly, HMNC-EPI overcomes both CMDR and NDR in human bladder cancer cell models, without using P-glycoprotein (P-gp) and nuclear pore inhibitors. Besides, the half-life of drug is prolonged ~1.8-fold (from 45 h to 81 h) at 37degC, with a ~ 10-fold increase in concentration at the tumor site through magnetic targeting (MT). Moreover, malignant NDR bladder cancer can be effectively inhibited after 14 days in mice by just two injections and MT. We are the first to demonstrate the nanomedical strategy that can overcome the CMDR and NDR bladder cancers simultaneously, and proceed to the excellent MT therapy, significantly reducing the dosage and cardiotoxicity and holding great promise for incurable human MDR bladder cancer.
机译:多药耐药性(MDR)是治愈癌症的主要障碍。细胞膜药物抗性(CMDR)和核药物抗性(NDR)都可能导致化学疗法失败,并且化学治疗剂的核输出尤其会降低化学疗法的抗癌效力。在这里,我们报告了由表柔比星(EPI)与无毒和高磁化纳米载体(HMNC)结合形成的一种激动人心的磁性靶向纳米药物。令人惊讶的是,HMNC-EPI在不使用P-糖蛋白(P-gp)和核孔抑制剂的情况下,在人膀胱癌细胞模型中克服了CMDR和NDR。此外,在37℃下,药物的半衰期延长了约1.8倍(从45小时到81小时),并且通过磁性靶向(MT)在肿瘤部位的浓度增加了约10倍。此外,只需两次注射和MT,即可在小鼠中14天后有效抑制恶性NDR膀胱癌。我们是第一个展示可以同时克服CMDR和NDR膀胱癌的纳米医学策略,并继续进行出色的MT治疗,显着降低剂量和心脏毒性,并为治愈人类MDR膀胱癌提供了广阔前景。

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  • 来源
    《The Journal of Urology》 |2013年第1期|共2页
  • 作者

    AtalaA.;

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  • 正文语种 eng
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  • 入库时间 2022-08-19 15:17:31

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