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In vivo culture of encapsulated endostatin-secreting Chinese hamster ovary cells for systemic tumor inhibition

  • Ying Zhang
  • , Wei Wang
  • , Yubing Xie
  • , Weiting Yu
  • , Huaining Teng
  • , Xiudong Liu
  • , Xulang Zhang
  • , Xin Guo
  • , Jian Fei
  • , Xiaojun Ma
  • CAS - Dalian Institute of Chemical Physics
  • University of Chinese Academy of Sciences
  • CAS - Shanghai Institute of Nutrition and Health

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Microencapsulation of recombinant cells is a novel alternative approach to tumor gene therapy. Therapeutic protein delivery can be sustained for systemic treatment of tumors because the recombinant cells are enclosed in microcapsules and the semipermeable membrane of the microcapsules protects the cells from host immune rejection and reduces the need for frequent injection. In this study, we describe a method to systemically inhibit tumor growth by in vivo culture of antiangiogenic endostatin-secreting Chinese hamster ovary (CHO) cells in microcapsules as small as 200 μm in diameter. Peritoneal administration of encapsulated endostatin-CHO cells inhibited melanoma growth to 66.4% and enhanced the survival of treated mice to 80% by 27 days posttreatment. Continuous systemic release of endostatin from microcapsules offers an effective therapeutic strategy to eradicate solid tumors.

Original languageEnglish
Pages (from-to)474-481
Number of pages8
JournalHuman Gene Therapy
Volume18
Issue number5
DOIs
StatePublished - May 2007

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