Bioactive properties and clinical safety of a novel milk protein peptide

Nutr J. 2011 Sep 26:10:99. doi: 10.1186/1475-2891-10-99.

Abstract

Background: Milk protein fractions and peptides have been shown to have bioactive properties. This preliminary study examined the potential mechanisms of action and clinical safety of novel milk protein peptide (MP).

Findings: A novel MP mixture inhibits the tyrosine kinase activity of epidermal growth factor receptor (EGFR), vascular endothelial growth factor receptor 2 (VEGFR2), and insulin receptor (IR) with IC50 of 9.85 μM, 7.7 μM, and 6.18 μM respectively. In vitro, this multi-kinase inhibitor causes apoptosis in HT-29 colon cancer cells, and in a C. elegans worm study, showed a weak but significant increase in lifespan. A six week double-blind, placebo-controlled study involving 73 healthy volunteers demonstrated that the MP mixture is safe to consume orally. All clinical blood markers remained within normal levels and no clinically significant side effects were reported. There was some evidence of improved insulin sensitivity, neutrophil-to-lymphocyte ratio (NLR), and quality of life assessment of role of physical function.

Conclusions: These data in combination with the observed in vitro anti-cancer properties warrant further clinical studies to investigate this MP mixture as a potential clinical nutrition intervention for improving the quality of life and clinical outcomes in cancer patients.

Trial registration: NCT01412658.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / growth & development
  • Cattle
  • Double-Blind Method
  • ErbB Receptors / antagonists & inhibitors
  • Female
  • HT29 Cells / drug effects
  • Humans
  • Inhibitory Concentration 50
  • Male
  • Middle Aged
  • Milk Proteins / pharmacology*
  • Milk Proteins / therapeutic use*
  • Protein Kinase Inhibitors / pharmacology*
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Receptor, Insulin / antagonists & inhibitors
  • Vascular Endothelial Growth Factor Receptor-2 / antagonists & inhibitors

Substances

  • Antineoplastic Agents
  • Milk Proteins
  • Protein Kinase Inhibitors
  • ErbB Receptors
  • Protein-Tyrosine Kinases
  • Receptor, Insulin
  • Vascular Endothelial Growth Factor Receptor-2

Associated data

  • ClinicalTrials.gov/NCT01412658