Abstract
Animal venoms possess variety of toxins/proteins/peptides which act as ionic channel inhibitors and target vital physiological processes. Toxin peptides isolated from honey bee, wasp and scorpion show membrane binding, growth inhibition and strong cytolytic properties. These also inhibit angiogenesis and induce caspase-dependent apoptosis in melanoma cells through the intrinsic mitochondrial pathway protecting the experimental animals against tumor development. These toxin peptides exert cytotoxic effects on human oral cancer cells by inducting apoptosis via a p53-dependent intrinsic apoptotic pathway. These can be used as cancer therapeutic agents by loading them in liposomes. This lead to increase in their target specificity against cancer cells, shorten cell survival, and produce higher reactive oxygen species (ROS), and does enhancement in the number of apoptotic cells. In addition, toxins enhance G0/G1 enrichment upon treatment of cancer cells. Further, encapsulated honey bee, wasp and scorpion venoms exert much potent anti-cancer effect on many cancer cells lines.