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One-shot dual gene editing for drug-resistant pancreatic cancer therapy

  • Eun Jeong Won
  • , Hyeji Park
  • , Seung Hee Chang
  • , Jin Hyun Kim
  • , Hojeong Kwon
  • , Young Seok Cho
  • , Tae Jong Yoon
  • Ajou University
  • Catholic Univ. of Korea Coll. Med.
  • Moogene Medi Institute
  • New York University

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

Abstract

It is challenging to diagnose patients with pancreatic ductal adenocarcinoma (PDAC) early on, and their treatment is often complex. Gemcitabine (GEM) is the first-line treatment for PDAC, but its efficacy is limited in most patients due to the GEM resistance from KRAS and P53 gene mutations. We describe the correction of a double gene mutation and therapeutic effect for the GEM resistant PDAC. Bio-available nanoliposomes (NL) possessing Cas9-ribonucleoproteins and adenine-base editors were developed to conduct KRAS and P53 mutation gene editing directly. NLs were conjugated with EGFR antibodies to tumor-specific delivery, and the anti-cancer effect was verified in vitro and in vivo Model. Our GEM-combinatorial therapeutic strategies using double gene editing systems with one-shot may be a potent therapy for PDAC, overcoming chemoresistance.

Original languageEnglish
Article number121252
JournalBiomaterials
Volume279
DOIs
StatePublished - Dec 2021

Bibliographical note

Publisher Copyright:
© 2021 Elsevier Ltd

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

  • Drug-resistance
  • Gene editing
  • Nanoliposome
  • Pancreatic cancer
  • Protein delivery

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