4.7 Article

Lucidin 3-methyl ether from Rubia philippinensis suppresses the proliferation of multiple myeloma cells through the promotion of β-catenin degradation

Journal

PHYTOMEDICINE
Volume 99, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.phymed.2022.153971

Keywords

Rubia philippinensis; Lucidin 3-methyl ether; Wnt/beta-catenin signaling; Multiple myeloma

Funding

  1. Fundamental Technology Program through the National Research Foundation of Korea (NRF) - Korean Government [NRF-2018R1D1A1B07048208, NRF-2020R1A2B5B01002415]
  2. Korea Environmental Industry and Technology Institute (KEITI) - Ministry of Environment of Korea

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Rubia philippinensis and its active metabolite lucidin 3-methyl ether prevent cell proliferation in multiple myeloma by suppressing the Wnt/beta-catenin pathway, making them potential chemopreventive agents for the treatment of MM.
Background: Constitutive accumulation of beta-catenin has been frequently observed in multiple myeloma. Extracts from genus Rubia plants exhibit cytotoxic activity against several types of cancer cells; however, little is known about their chemopreventive mechanisms and bioactive metabolites. Purpose: Purpose: The study aimed to identify the underlying antiproliferative mechanisms of Rubia philippinensis extract in multiple myeloma cells and the major active metabolites responsible for cytotoxic activity of R. philippinensis. Methods: The effects of R. philippinensis extracts and lucidin 3-methyl ether on the Wnt/beta-catenin pathway were determined by cell-based reporter assay, Western blot analysis, and RT-PCR. The antiproliferative activity was evaluated by cell viability assay and apoptosis analysis in RPMI8226 and MM.1S multiple myeloma cells. Results: R. philippinensis extracts inhibited Wnt/beta-catenin signaling and lucidin 3-methyl ether, an anthraquinone derivative, was identified as the major active metabolite responsible for the inhibition of Wnt/beta-catenin signaling. Lucidin 3-methyl ether induced beta-catenin phosphorylation at Ser33/Ser37/Thr41 residues and promoted proteasomal degradation of beta-catenin via a GSK-313-independent mechanism, thereby downregulating Wnt3a-induced beta-catenin response transcription (CRT). Moreover, lucidin 3-methyl ether repressed the expression of beta-catenin/T-cell factor (TCF)-dependent genes, such as cyclin D1, c-myc, and axin-2, thus inhibiting MM cell proliferation. Apoptosis was also elicited by lucidin 3-methyl ether, as indicated by the increase in the population of annexin V-FITC positive cells and caspase-3/7 activity in MM cells. Conclusion: These findings indicate that R. philippinensis and its active metabolite lucidin 3-methyl ether prevent cell proliferation through the suppression of the Wnt/beta-catenin pathway and exhibit potential as chemopreventive agents for the treatment of MM.

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