A modified arginine-depleting enzyme NEI-01 inhibits growth of pancreatic cancer cells

PLoS One. 2020 Apr 30;15(4):e0231633. doi: 10.1371/journal.pone.0231633. eCollection 2020.

Abstract

Arginine deprivation cancer therapy targets certain types of malignancies with positive result in many studies and clinical trials. NEI-01 was designed as a novel arginine-depleting enzyme comprising an albumin binding domain capable of binding to human serum albumin to lengthen its half-life. In the present work, NEI-01 is shown to bind to serum albumin from various species, including mice, rat and human. Single intraperitoneal administration of NEI-01 to mice reduced plasma arginine to undetectable level for at least 9 days. Treatment of NEI-01 specifically inhibited cell viability of MIA PaCa-2 and PANC-1 cancer cell lines, which were ASS1 negative. Using a human pancreatic mouse xenograft model, NEI-01 treatment significantly reduced tumor volume and weight. Our data provides proof of principle for a cancer treatment strategy using NEI-01.

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / therapeutic use*
  • Arginine / blood
  • Arginine / deficiency
  • Arginine / metabolism*
  • Argininosuccinate Synthase / metabolism
  • Carcinoma / drug therapy*
  • Cell Line, Tumor
  • Female
  • Humans
  • Injections, Intraperitoneal
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Pancreatic Neoplasms / drug therapy*
  • Protein Binding
  • Protein-Arginine Deiminases / administration & dosage
  • Protein-Arginine Deiminases / metabolism
  • Protein-Arginine Deiminases / therapeutic use*
  • Rats
  • Serum Albumin / metabolism

Substances

  • Antineoplastic Agents
  • Serum Albumin
  • Arginine
  • Protein-Arginine Deiminases
  • Argininosuccinate Synthase

Grants and funding

New Epsilon Innovation Limited provided support for this study in the form of salaries for authors (JPHC, YC, DTLC, SHKC, KCC, KYN, OML, RMHW, AWLL, YOL, SYK). The specific roles of these authors are articulated in the ‘author contributions’ section. Beyond employment, New Epsilon Innovation Limited had no other role in the study design, data collection and analysis, and preparation of the manuscript.