Evaluation on anticancer effect against HL-60 cells and toxicity in vitro and in vivo of the phenethyl acetate isolated from a marine bacterium Streptomyces griseusopen access
- Authors
- Lee, Ji-Hyeok; Zhang, Chao; Ko, Ju-Young; Lee, Jung-Suck; Jeon, You-Jin
- Issue Date
- Mar-2015
- Publisher
- Korean Fisheries Society
- Keywords
- Anti-cancer activity; Marine bacteria; Secondary metabolite; Streptomyces griseus; Toxicity
- Citation
- Fisheries and Aquatic Sciences, v.18, no.1, pp 35 - 44
- Pages
- 10
- Indexed
- SCOPUS
KCI
- Journal Title
- Fisheries and Aquatic Sciences
- Volume
- 18
- Number
- 1
- Start Page
- 35
- End Page
- 44
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/77443
- DOI
- 10.5657/FAS.2015.0035
- ISSN
- 2234-1749
2234-1757
- Abstract
- We previously identified Streptomyces griseus as an anti-cancer agent (Kim et al., 2014). In this study, we isolated compounds from S. griseus and evaluated their anticancer effect and toxicity in vitro and in vivo. Preparative centrifugal partition chromatography (CPC) was used to obtain three compounds, cyclo(L-[4-hydroxyprolinyl]- L –leucine], cyclo(L-Phe-trans-4-hydroxy-L-Pro) and phenethyl acetate (PA). We chose PA, which had the highest anticancer activity, as a target compound for further experiments. PA induced the formation of apoptotic bodies, DNA fragmentation, DNA accumulation in G0/G1 phase, and reactive oxygen species (ROS) formation. Furthermore, PA treatment increased Bax/Bcl-xL expression, activated caspase-3, and cleaved poly-ADP-ribose polymerase (PARP) in HL-60 cells. Simultaneous evaluation in vitro and in vivo, revealed that PA exhibited no toxicity in Vero cells and zebrafish embryos. We revealed, for the first time, that PA generates ROS, and that this ROS accumulation induced the Bcl signaling pathway. © 2015 The Korean Society of Fisheries and Aquatic Science.
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