The inhibitory effect of roasted licorice extract on human metastatic breast cancer cell-induced bone destruction

Sun Kyoung Lee, Kwang Kyun Park, Jung Han Yoon Park, Soon Sung Lim, Won Yoon Chung

Research output: Contribution to journalArticlepeer-review

29 Citations (Scopus)


The aim of this study was to determine whether the ethanol extract of roasted licorice (rLE) could inhibit breast cancer-mediated bone destruction. rLE treatment reduced the viability of MDA-MB-231 human metastatic breast cancer cells but did not show any cytotoxicity in hFOB1.19 human osteoblastic cells and murine bone marrow-derived macrophages (BMMs). rLE inhibited expression and secretion of receptor activator of nuclear factor κB ligand (RANKL) as well as the mRNA and protein expression of cyclooxygenase-2 in osteoblastic cells exposed to the conditioned medium of breast cancer cells. rLE dramatically inhibited RANKL-induced osteoclastogenesis in BMMs, thereby reducing osteoclast-mediated pit formation. Moreover, treatment with licochalcone A and isoliquiritigenin as the active components, whose contents are increased by the roasting process, remarkably suppressed RANKL-induced osteoclast formation in BMMs, respectively. Furthermore, orally administered rLE substantially blocked tumor growth and bone destruction in mice inoculated with breast cancer cells in the tibiae. Serum levels of tartrate-resistant acid phosphatase and C-terminal cross-linking telopeptide of type I collagen and trabecular bone morphometric parameters were reversed to almost the same levels as the control mice by the rLE treatment. In conclusion, rLE may be a beneficial agent for preventing and treating bone destruction in patients with breast cancer.

Original languageEnglish
Pages (from-to)1776-1783
Number of pages8
JournalPhytotherapy Research
Issue number12
Publication statusPublished - 2013 Dec

All Science Journal Classification (ASJC) codes

  • Pharmacology


Dive into the research topics of 'The inhibitory effect of roasted licorice extract on human metastatic breast cancer cell-induced bone destruction'. Together they form a unique fingerprint.

Cite this