Antiproliferative and apoptotic activity of Chamaecyparis obtusa leaf extract against the HCT116 human colorectal cancer cell line and investigation of the bioactive compound by gas chromatography-mass spectrometry-based metabolomics

Hye Youn Kim, Seul Gi Lee, Taek Joo Oh, Sa Rang Lim, So Hyun Kim, Hong Jin Lee, Young Suk Kim, Hyung Kyoon Choi

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Chamaecyparis obtusa (CO) belongs to the Cupressaceae family, and it is found widely distributed in Japan and Korea. In this study, the anti-proliferative activities of the methanol and water extracts of CO leaves against a human colorectal cancer cell line (HCT116) were investigated. The methanol extract of CO leaves, at a concentration of 1.25 μg/mL, exhibited anti-proliferative activity against HCT116 cells, while displaying no cytotoxicity against Chang liver cells. Comparative global metabolite profiling was performed using gas chromatography-mass spectrometry coupled with multivariate statistical analysis, and it was revealed that anthricin was the major compound contributing to the anti-proliferative activity. The activation of c-Jun N-terminal kinases played a key role in the apoptotic effect of the methanol extract of CO leaves in HCT116 human colon cancer cells. These results suggest that the methanol extract and anthricin derived from CO leaves might be useful in the development of medicines with anti-colorectal cancer activity.

Original languageEnglish
Pages (from-to)18066-18082
Number of pages17
JournalMolecules
Volume20
Issue number10
DOIs
StatePublished - 2 Oct 2015

Bibliographical note

Publisher Copyright:
© 2015 by the authors; licensee MDPI, Basel, Switzerland.

Keywords

  • Anthricin
  • Chamaecyparis obtusa
  • Gas chromatography-mass spectrometry
  • Human colorectal cancer
  • Metabolite profiling

Fingerprint

Dive into the research topics of 'Antiproliferative and apoptotic activity of Chamaecyparis obtusa leaf extract against the HCT116 human colorectal cancer cell line and investigation of the bioactive compound by gas chromatography-mass spectrometry-based metabolomics'. Together they form a unique fingerprint.

Cite this