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Nanomaterials and Block Copolymers for Overcoming Multidrug Resistance in Cancer.

机译:用于克服癌症中多药耐药性的纳米材料和嵌段共聚物。

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摘要

The development of multidrug resistance in cancer is one of the leading causes for decreased chemotherapy efficacy and is particularly threatening to aggressive cancers such as that of the pancreas. In cancers where chemotherapy is amongst the few treatment options, it is crucial to develop chemotherapeutics that either bypass or control the development of multidrug resistance. Polymeric nanomaterials such as PluronicsRTM are of current interest due to their ability to perform these functions in addition to enhancing pro-apoptotic mechanisms. Using the respectively known chemosensitive and chemoresistant pancreatic adenocarcinoma cell lines MiaPaCa-2 and PANC-1, an in vitro analysis of the synergistic effect using 5-fluorouracil in conjugation with PluronicRTM F127 was performed. By monitoring cell viability and regulation of cell cycle, we were able to show that compared to the use of 5-flurouracil alone, there was enhanced cytotoxicity when using drug associated with PluronicRTM F127 in MiaPaCa-2 cells. The more chemoresistant cell line PANC-1 showed no significant enhancement of 5-fluorouracil cytotoxicity when associated with PluronicRTM F127. Enhanced cytotoxicity due to the use of PluronicRTM F127 may potentially become an exploitable feature for novel chemotherapeutic development in the future.
机译:癌症中多药耐药性的发展是化学疗法功效下降的主要原因之一,并且特别威胁到侵袭性癌症,例如胰腺癌。在化学疗法是少数治疗方案之一的癌症中,至关重要的是开发能够绕开或控制多药耐药性发展的化学疗法。诸如PluronicsRTM之类的聚合物纳米材料由于其除了增强促凋亡机制外还具有执行这些功能的能力,因此引起了人们的关注。使用分别已知的化学敏感性和化学抗性胰腺腺癌细胞系MiaPaCa-2和PANC-1,对5-氟尿嘧啶与PluronicRTM F127结合进行了协同作用的体外分析。通过监测细胞活力和调节细胞周期,我们能够证明,与单独使用5-氟尿嘧啶相比,在MiaPaCa-2细胞中使用与PluronicRTM F127相关的药物时,细胞毒性增强。当与PluronicRTM F127结合时,具有更高化学耐药性的细胞系PANC-1不会显着增强5-氟尿嘧啶的细胞毒性。由于使用PluronicRTM F127而增强的细胞毒性可能在将来成为新型化学疗法开发的可利用功能。

著录项

  • 作者

    Livingston, Wesley.;

  • 作者单位

    Loma Linda University.;

  • 授予单位 Loma Linda University.;
  • 学科 Oncology.;Materials science.
  • 学位 M.S.
  • 年度 2011
  • 页码 73 p.
  • 总页数 73
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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