Controlled release strategy of paclitaxel by conjugating to matrix metalloproteinases-2 sensitive peptide

Oncotarget. 2016 Aug 9;7(32):52230-52238. doi: 10.18632/oncotarget.10735.

Abstract

Peptide drug conjugates offer a novel strategy to achieve controlled drug release. This approach avoids the clinical obstacles of non-specific toxicity and overall drug resistance of conventional cytotoxic agents, such as paclitaxel. MMP2 plays important functions in tumour proliferation and metastasis. Herein, we conjugated the paclitaxel with a hexapeptide which is specific recognized by MMP2 protein. The conjugate is dissociated upon the MMP2 specific proteolysis at COOH terminal of hexapeptide, PVGLIG.The results clearly indicated that the PVGLIG-paclitaxel conjugate significantly enhanced the tumor specificity against HT-1080 and U87-MG tumour cells. Our finding suggested that the hexapeptide PVGLIG is capable to act as a controlled and sustained drug carrier of paclitaxel for the treatment against tumour proliferation and metastasis with high MMP2 expression.

Keywords: drug conjugate; matrix metalloproteinase; paclitaxel; tumor metastasis; tumor targeting peptide.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / chemical synthesis
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Cell Line, Tumor
  • Delayed-Action Preparations / chemical synthesis
  • Delayed-Action Preparations / pharmacology
  • Drug Carriers / chemical synthesis
  • Drug Carriers / pharmacology*
  • Humans
  • Matrix Metalloproteinase 2 / metabolism*
  • Mice
  • Paclitaxel / administration & dosage*
  • Peptides / chemical synthesis
  • Peptides / pharmacology
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents, Phytogenic
  • Delayed-Action Preparations
  • Drug Carriers
  • Peptides
  • Matrix Metalloproteinase 2
  • Paclitaxel