4.7 Review

Recent developments in animal venom peptide nanotherapeutics with improved selectivity for cancer cells

Journal

BIOTECHNOLOGY ADVANCES
Volume 50, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2021.107769

Keywords

Venom peptides; Cancer; Selectivity; Nanoparticles; Nanotherapeutics; Conjugation; Delivery; Drug leads

Funding

  1. Intramural Research Program of the National Cancer Institute, National Institutes of Health, USA [ZIA BCE 012004]

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Animal venoms contain bioactive peptides that modulate cellular excitability and show potential in anticancer therapy. Strategies such as bioconjugation and nanotechnologies could enhance the selectivity and potency of venom peptides against cancer cells.
Animal venoms are a rich source of bioactive peptides that efficiently modulate key receptors and ion channels involved in cellular excitability to rapidly neutralize their prey or predators. As such, they have been a wellspring of highly useful pharmacological tools for decades. Besides targeting ion channels, some venom peptides exhibit strong cytotoxic activity and preferentially affect cancer over healthy cells. This is unlikely to be driven by an evolutionary impetus, and differences in tumor cells and the tumor microenvironment are probably behind the serendipitous selectivity shown by some venom peptides. However, strategies such as bioconjugation and nanotechnologies are showing potential to improve their selectivity and potency, thereby paving the way to efficiently harness new anticancer mechanisms offered by venom peptides. This review aims to highlight advances in nano- and chemotherapeutic tools and prospective anti-cancer drug leads derived from animal venom peptides.

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