Ki, J-S., Hwang, D-S., Shin, K., Yoon, W. D., Lim, D., Kang, Y. S., Lee, Y., and Lee, J-S. 2008. Recent moon jelly (Aurelia sp.1) blooms in Korean coastal waters suggest global expansion: examples inferred from mitochondrial COI and nuclear ITS-5.8S rDNA sequences. – ICES Journal of Marine Science, 65: 443–452. The moon jelly Aurelia was found recently in Korean coastal environments, and its dense blooms caused economic losses for fisheries and power plants. The species is tentatively recognized as Aurelia aurita; yet, its identity and origin remain elusive. To find reliable molecular evidence for its identity, we determined the DNA sequence of the mitochondrial cytochrome c oxidase subunit I gene and nuclear ITS-5.8S rDNA of specimens collected from different Korean locations. We compared the nuclear and mitochondrial DNA data among specimens and demonstrated that all Korean Aurelia have an identical genotype. BLAST searches demonstrated that the Korean Aurelia matched the previously designated Aurelia sp.1. Parsimony and relevant phylogenetic analyses of the genus Aurelia demonstrated that the genotypes of Korean, Japanese, and Californian Aurelia sp.1 were nearly identical (>99.6% similarity), whereas they were significantly different (<84.1% similarity) from other Aurelia. This suggests that Aurelia sp.1, which occur in the three regions, are descendants of a single population and may have dispersed from one location. However, the dispersal time and origin of Aurelia sp.1 still remain uncertain.

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Various kinds of animal venoms and their components have been widely studied for potential therapeutic applications. This study evaluated whether Nemopilema nomurai jellyfish venom (NnV) has anticancer activity. NnV strongly induced cytotoxicity of HepG2 cells through apoptotic cell death, as demonstrated by alterations of chromatic morphology, activation of procaspase-3, and an increase in the Bax/Bcl-2 ratio. Furthermore, NnV inhibited the phosphorylation of PI3K, PDK1, Akt, mTOR, p70S6K, and 4EBP1, whereas it enhanced the expression of p-PTEN. Interestingly, NnV also inactivated the negative feedback loops associated with Akt activation, as demonstrated by downregulation of Akt at Ser473 and mTOR at Ser2481. The anticancer effect of NnV was significant in a HepG2 xenograft mouse model, with no obvious toxicity. HepG2 cell death by NnV was inhibited by tetracycline, metalloprotease inhibitor, suggesting that metalloprotease component in NnV is closely related to the anticancer effects. This study demonstrates, for the first time, that NnV exerts highly selective cytotoxicity in HepG2 cells via dual inhibition of the Akt and mTOR signaling pathways, but not in normal cells.