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      Selective Targeting and Eradication of LGR5+ Cancer Stem Cells Using RSPO-Conjugated Doxorubicin Liposomes.

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          Abstract

          Cancer stem cells (CSC) that may account for only a small fraction of tumor mass were found to play crucial roles during tumor initiating, progression, and metastasis. However, they are usually difficult to be treated and notoriously resilient to drug eradication. In this study, we aimed at the Wnt signaling characteristic of CSCs and designed a liposomal drug delivery system to target CSCs. Liposomes decorated with RSPO1 on the surface were constructed for specific interactions with the Wnt pathway coreceptor LGR5. Doxorubicin carried by the RSPO1-liposomes was more effective at lower concentrations than the same drug loaded in PEG-liposomes. More importantly, we showed using a patient-derived xenograft tumor model where LGR5+ CSCs coexisted with LGR5- cells, the RSPO1-liposomes were able to access more CSC cells and deliver the drug specifically and efficiently. Such a focused effect in eradicating LGR5+ cells led to massive tumor tissue necrosis and growth inhibition even when only a fraction of the conventional drug dose was used. These data clearly demonstrated the advantages of CSC-targeted drug delivery and would support the development of such approaches as a new cancer treatment strategy. Mol Cancer Ther; 17(7); 1475-85. ©2018 AACR.

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          Author and article information

          Journal
          Mol Cancer Ther
          Molecular cancer therapeutics
          American Association for Cancer Research (AACR)
          1538-8514
          1535-7163
          July 2018
          : 17
          : 7
          Affiliations
          [1 ] Shanghai Jiaotong University, School of Pharmacy, Shanghai, China.
          [2 ] Shanghai Jiaotong University, School of Pharmacy, Shanghai, China. yhxu@sjtu.edu.cn.
          [3 ] College of Pharmacy and Chemistry, Dali University, Dali, China.
          Article
          1535-7163.MCT-17-0694
          10.1158/1535-7163.MCT-17-0694
          29695632
          8a81792d-36da-4c75-bdab-8be66a427166
          ©2018 American Association for Cancer Research.
          History

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