β-Thujaplicin modulates estrogen receptor signaling and inhibits proliferation of human breast cancer cells

  • Jiwon Ko
  • , Cheng Bao
  • , Hyun Chang Park
  • , Minchae Kim
  • , Hyung Kyoon Choi
  • , Young Suk Kim
  • , Hong Jin Lee

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

β-Thujaplicin, one of the major constituents in Chamaecyparis obtusa, has been demonstrated to exert different health beneficial efficacy, but the role of β-thujaplicin in regulating mammary tumorigene-sis has not been investigated. In this study, we found that β-thujaplicin significantly suppressed the proliferation through arresting the cell cycle transition from G1 to S phase as well as inhibited the expression of cell cycle-related proteins, cyclin D1, and cyclin-dependent kinase 4 (CDK4) in MCF-7 and T47D luminal subtype breast cancer cells. In addition, estrogen receptor α (ER-α) was down-regulated by β-thujaplicin via enhanced proteolysis by ubiqui-tination, which led to cell growth inhibition. These results suggest that β-thujaplicin may be considered as a potent agent regulating the hormone sensitive mammary tumorigenesis.

Original languageEnglish
Pages (from-to)1011-1017
Number of pages7
JournalBioscience, Biotechnology and Biochemistry
Volume79
Issue number6
DOIs
StatePublished - 2015

Bibliographical note

Publisher Copyright:
© 2015 Japan Society for Bioscience, Biotechnology, and Agrochemistry.

Keywords

  • Breast cancer
  • Cyclin D1
  • Estrogen receptor
  • Ubiquitination
  • β-thujaplicin

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