A modified arginine-depleting enzyme NEI-01 inhibits growth of pancreatic cancer cells.
Jeremy P H ChowYijun CaiDaniel T L ChowSteven H K ChungKa-Chun ChauKa-Ying NgOscar M LeungRaymond M H WongAlan W L LawYu-On LeungSui-Yi KwokYun-Chung LeungPublished in: PloS one (2020)
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.
Keyphrases
- nitric oxide
- endothelial cells
- clinical trial
- cancer therapy
- human serum albumin
- oxidative stress
- drug delivery
- body mass index
- randomized controlled trial
- metabolic syndrome
- squamous cell carcinoma
- type diabetes
- pluripotent stem cells
- weight gain
- papillary thyroid
- young adults
- electronic health record
- adipose tissue
- skeletal muscle
- transcription factor
- phase ii
- data analysis
- wild type