Tailored protein-conjugated DNA nanoplatform for synergistic cancer therapy

J Control Release. 2022 Jun:346:250-259. doi: 10.1016/j.jconrel.2022.04.022. Epub 2022 Apr 27.

Abstract

Multidrug resistance (MDR) to chemotherapeutic drugs and targeted drug delivery are recurring issues in clinical cancer treatment. Here, a multifunctional fusion protein-DNA conjugate was designed as a co-delivery vehicle for anticancer peptides and chemotherapeutic drugs to combat both drug-resistant and drug-sensitive tumor cells. The fusion protein was constructed by fusing a PsTag polypeptide, a matrix metalloproteinase 2 (MMP2)-degradable domain, and the mitochondria-targeted pro-apoptotic peptide KLAKLAKKLAKLAK. Doxorubicin was efficiently loaded into the fusion protein pre-conjugated dendrimer-like DNA nanostructure. With the incorporation of enhanced stability, tumor targeting, and controlled-release elements, the tailored nanostructure can selectively enter tumor cells and synergistically exert antitumor activity with no significant adverse effects. Thus, these protein-conjugated DNA nanocarriers could be a potential co-delivery system for protein/peptide and chemotherapeutic drugs delivery in synergistic cancer therapy.

Keywords: Cancer; DNA nanotechnology; Drug delivery; Multidrug resistance; Peptide therapeutics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents* / administration & dosage
  • Cell Line, Tumor
  • DNA
  • Doxorubicin
  • Drug Delivery Systems*
  • Drug Resistance, Neoplasm
  • Humans
  • Matrix Metalloproteinase 2
  • Nanoparticles
  • Neoplasms* / drug therapy
  • Neoplasms* / pathology
  • Peptides / chemistry

Substances

  • Antineoplastic Agents
  • Peptides
  • Doxorubicin
  • DNA
  • Matrix Metalloproteinase 2