Pharbilignan C induces apoptosis through a mitochondria-mediated intrinsic pathway in human breast cancer cells
- Authors
- Park, Yong Joo; Choi, Chang-Ik; Chung, Kyu Hyuck; Kim, Ki Hyun
- Issue Date
- 1-Oct-2016
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Keywords
- Pharbilignan C; Pharbitis nil; Antiproliferative; Apoptosis; Intrinsic pathway
- Citation
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.26, no.19, pp 4645 - 4649
- Pages
- 5
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Volume
- 26
- Number
- 19
- Start Page
- 4645
- End Page
- 4649
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/24942
- DOI
- 10.1016/j.bmcl.2016.08.054
- ISSN
- 0960-894X
1464-3405
- Abstract
- Pharbitidis Semen, the seed of Morning glory (Pharbitis nil), is a medicinal agent that has traditionally been used as a purgative in Korea. Pharbilignan C (PLC) is a dihydro[b]-benzofuran-type neolignan from Pharbitidis Semen, which reportedly exhibited the most potent cytotoxicity against human tumor cells. To further study the antiproliferative activity of PLC, its molecular mechanisms of action in two breast adenocarcinoma cells, MCF-7 and MDA-MB 231 cells were investigated. PLC inhibited the proliferation of MDA-MB 231 and MCF-7 cells, in order of sensitivity (IC50 of MDA-MB 231 cells: 7.0 +/- 2.0 mu M). PLC induced apoptosis in MDA-MB 231 cells with down regulation of Bcl-2 and up-regulation of Bax expression. It also decreased mitochondrial membrane potential accompanied with increasing initiator caspase, caspase-9 activation and executioner caspase, caspase-3 activation. This study demonstrates that PLC inhibited proliferation of MDA-MB 231 cells by inducing apoptosis via the mitochondria-mediated intrinsic pathway. (C) 2016 Elsevier Ltd. All rights reserved.
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