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Cytotoxic effect of sanguiin H-6 on MCF-7 and MDA-MB-231 human breast carcinoma cells

Authors
Park, Eun-JiLee, DahaeBaek, Seon-EunKim, Ki HyunKang, Ki SungJang, Tae SuLee, Hye LimSong, Ji HoonYoo, Jeong-Eun
Issue Date
15-Sep-2017
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Sanguiin H-6; Apoptosis; Estrogen receptor; MCF-7 cells; MDA-MB-231 cells
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.27, no.18, pp.4389 - 4392
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume
27
Number
18
Start Page
4389
End Page
4392
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/5708
DOI
10.1016/j.bmcl.2017.08.019
ISSN
0960-894X
Abstract
Sanguiin H-6 is a dimer of casuarictin linked by a bond between the gallic acid residue and one of the hexahydroxydiphenic acid units. It is an effective compound extracted from Rubus coreanus. It has an anticancer effect against several human cancer cells; however, its effect on breast cancer cells has not been clearly demonstrated. Thus, we aimed to investigate the anticancer effect and mechanism of action of sanguiin H-6 against two human breast carcinoma cell lines (MCF-7 and MDA-MB-231). We found that sanguiin H-6 significantly reduced cell viability in a concentration-dependent manner. It also increased the rates at which MCF-7 and MDA-MB-231 cells underwent apoptosis. Furthermore, sanguiin H-6 induced the cleavage of caspase-8, caspase-3, and poly(ADP-ribose) polymerase, which resulted in apoptosis. However, cleavage of caspase-9 was only detectable in MCF-7 cells. In addition, sanguiin H-6 increased the ratio of Bax to Bcl-2 in both MCF-7 and MDA-MB-231 cells. These findings suggest that sanguiin H-6 is a potent therapeutic agent against breast cancer cells. In addition, it exerts its anticancer effect in an estrogen-receptor-independent manner. (C) 2017 Elsevier Ltd. All rights reserved.
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College of Korean Medicine (Premedical course of Oriental Medicine)
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