Novel anticancer activity of phloroglucinol against breast cancer stem-like cells
- Authors
- Kim, Rae-Kwon; Uddin, Nizam; Hyun, Jin-Won; Kim, Changil; Suh, Yongjoon; Lee, Su-Jae
- Issue Date
- Aug-2015
- Publisher
- Academic Press
- Keywords
- Phloroglucinol; Breast cancer stem-like cells; Relapse; Resistance to anticancer treatment; KRAS; Anticancer activity
- Citation
- Toxicology and Applied Pharmacology, v.286, no.3, pp 143 - 150
- Pages
- 8
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Toxicology and Applied Pharmacology
- Volume
- 286
- Number
- 3
- Start Page
- 143
- End Page
- 150
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/24905
- DOI
- 10.1016/j.taap.2015.03.026
- ISSN
- 0041-008X
1096-0333
- Abstract
- Poor prognosis of breast cancer patients is closely associated with metastasis and relapse. There is substantial evidence supporting that cancer stem-like cells (CSCs) are primarily responsible for relapse in breast cancer after anticancer treatment. However, there is a lack of suitable drugs that target breast cancer stem-like cells (BCSCs). Here, we report that phloroglucinol (PG), a natural phlorotannin component of brown algae, suppresses sphere formation, anchorage-independent colony formation and in vivo tumorigenicity. In line with these observations, treatment with PG also decreased CD44(+) cancer cell population as well as expression of CSC regulators such as Sox2, CD44, Oct4, Notch2 and beta-catenin. Also, treatment with PG sensitized breast cancer cells to anticancer drugs such as cisplatin, etoposide, and taxol as well as to ionizing radiation. Importantly, PG inhibited KRAS and its downstream PI3K/AKT and RAF-1/ERK signaling pathways that regulate the maintenance of CSCs. Taken together, our findings implicate PG as a good candidate to target BCSCs and to prevent the disease relapse. (C) 2015 Elsevier Inc. All rights reserved.
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