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(-)-9'-O-(alpha-L-Rhamnopyranosyl) lyoniresinol from Lespedeza cuneata suppresses ovarian cancer cell proliferation through induction of apoptosis

Authors
Baek, JiwonLee, DahaeLee, Tae KyoungSong, Ji HoonLee, Ju SungLee, SeongYoo, Sang-WooKang, Ki SungMoon, EunjungLee, SanghyunKim, Ki Hyun
Issue Date
15-Jan-2018
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Lespedeza cuneata; Fabaceae; (-)-9 ' -O-(alpha-L-Rhamnopyranosyl) lyoniresinol; A2780 ovarian carcinoma cells; Apoptosis; Caspase
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.28, no.2, pp.122 - 128
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume
28
Number
2
Start Page
122
End Page
128
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4162
DOI
10.1016/j.bmcl.2017.11.045
ISSN
0960-894X
Abstract
Lespedeza cuneata (Dum. Cours.) G. Don. (Fabaceae), known as Chinese bushclover or sericea lespedeza, has been used in traditional medicine to treat diabetes, hematuria, and insomnia, and it has been reported that bioactive compounds from L. cuneata possess various pharmacological properties. However, there has been no study to determine the active compounds from L. cuneata with potential activity against ovarian cancer. This study aimed to isolate cytotoxic compounds from L. cuneata and identify the molecular mechanisms underlying the apoptosis pathway in ovarian cancer cells. Based on cytotoxic activity identified in the screening test, chemical investigation of the active fraction of L. cuneata led to the isolation of nine compounds including four lignanosides (1-4), three flavonoid glycosides (5-7), and two phenolics (8-9). Cytotoxicity and the molecular mechanism were examined by methyl thiazolyl tetrazolium (MTT) assay and Western blot analysis. Of the isolated compounds, (-)-9'-O-(alpha-L-rhamnopyranosyl) lyoniresinol (3) demonstrated the strongest effect in suppressing A2780 human ovarian carcinoma cell proliferation in a dose-dependent manner, with an IC50 value of 35.40 +/- 2.78 mu M. Control A2780 cells had normal morphology, whereas cell blebbing, shrinkage, and condensation were observed after treatment with compound 3. Western blotting analysis showed that compound 3 inhibited A2780 human ovarian cancer cell viability by activating caspase-8, caspase-3, and PARP, which contributed to apoptotic cell death. These results suggest that (-)- 9'-O-(a-L-rhamnopyranosyl) lyoniresinol (3) has potent anticancer activities against A2780 human ovarian carcinoma cells through the extrinsic apoptotic pathway. Therefore, (-)- 9'-O-(alpha-L-rhamnopyranosyl) lyoniresinol is an excellent candidate for the development of novel chemotherapeutics. (C) 2017 Elsevier Ltd. All rights reserved.
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College of Korean Medicine (Premedical course of Oriental Medicine)
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