Abstract

We showed recently that nerve growth factor (NGF) from cobra venom inhibited the growth of Ehrlich ascites carcinoma (EAC) inoculated subcutaneously in mice. Here, we studied the influence of anti-complementary cobra venom factor (CVF) and the non-steroidal anti-inflammatory drug ketoprofen on the antitumor NGF effect, as well as on NGF-induced changes in EAC histological patterns, the activity of lactate and succinate dehydrogenases in tumor cells and the serum level of some cytokines. NGF, CVF and ketoprofen reduced the tumor volume by approximately 72%, 68% and 30%, respectively. The antitumor effect of NGF was accompanied by an increase in the lymphocytic infiltration of the tumor tissue, the level of interleukin 1β and tumor necrosis factor α in the serum, as well as the activity of lactate and succinate dehydrogenases in tumor cells. Simultaneous administration of NGF with either CVF or ketoprofen abolished the antitumor effect and reduced all other effects of NGF, whereas NGF itself significantly decreased the antitumor action of both CVF and ketoprofen. Thus, the antitumor effect of NGF critically depended on the status of the immune system and was abolished by the disturbance of the complement system; the disturbance of the inflammatory response canceled the antitumor effect as well.

Highlights

  • Nerve growth factor (NGF) belongs to a protein family of neurotrophins, which are important agents affecting the cell cycle

  • cobra venom factor (CVF) and ketoprofen, through various mechanisms, counteract the development of an inflammatory tumor microenvironment. To check if these drugs act synergistically with nerve growth factor (NGF), we have studied the influence of CVF and ketoprofen on the antitumor effects of cobra venom NGF in vivo

  • NGF inhibited the tumor growth by about 72%, which was in accordance with our thepreviously tumor growth by about

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Summary

Introduction

Nerve growth factor (NGF) belongs to a protein family of neurotrophins, which are important agents affecting the cell cycle. They are mitogens; mammalian NGF has evident regenerative (primarily neuroprotective) functions. NGF can bind to two classes of receptors on the cell surface: the TrkA receptor, a tyrosine kinase with high specificity and high affinity to NGF, and p75, a low-affinity neurotrophin receptor which can Toxins 2017, 9, 274; doi:10.3390/toxins9090274 www.mdpi.com/journal/toxins. Toxins 2017, 9, 274 bind to all members of the neurotrophin family with approximately equal affinity.

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