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A liver-tumor adhesion peptide from random phage display library

  • Miao Wu
  • , Bing Du
  • , Lei Wang
  • , Zhong Liang Zhou
  • , Min Qian*
  • *Corresponding author for this work
  • East China Normal University

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: To identify and localize the synthesized targeting peptide A54 to liver cancer cell line BEL-7402 in vivo and in vitro for confirming the potential clinical application of peptide A54 in hepatocarcinoma targeting therapy. Methods: Phage A54 was confirmed by ELISA. Biotin and FAM labeled A54 peptides were identified and localized by means of immunohistochemistry and immunocytochemistry. Results: A54 peptide could target the liver-tumor tissue in vivo and adhere to several liver-tumor cells in vitro. FAM-labeled A54 peptides were localized on the membrane surface of liver-tumor cells. Conclusion: Synthesized A54 peptide obtained from in vivo phage display technology still kept special ability to adhere liver-tumor cell in vivo and in vitro. The A54 peptide could be a candidate carrier for hepatocarcinoma targeting therapy.

Original languageEnglish
Pages (from-to)241-245
Number of pages5
JournalChinese Journal of Cancer Research
Volume18
Issue number4
DOIs
StatePublished - Dec 2006

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • A54 peptide
  • Identification
  • Localization
  • Medicine carrier

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