Papers

Peer-reviewed
Sep, 2017

Identification of a novel component leading to anti-tumor activity besides the major ingredient cordycepin in Cordyceps militaris extract

JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
  • Takeharu Wada
  • ,
  • I. Wayan Sumardika
  • ,
  • Shingo Saito
  • ,
  • I. Made Winarsa Ruma
  • ,
  • Eisaku Kondo
  • ,
  • Masami Shibukawa
  • ,
  • Masakiyo Sakaguchi

Volume
1061
Number
First page
209
Last page
219
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1016/j.jchromb.2017.07.022
Publisher
ELSEVIER SCIENCE BV

In accordance with our previous study that was carried out to identify novel anti-tumor ingredients, chromatographic separation in combination with an anti-tumor activity assay was used for analysis of Cordyceps militaris extract in this study. Various modes of chromatography including reversed-phase, cation-exchange and anion exchange were used to separate components of Cordyceps militaris, which showed various chemical properties. Anti-tumor activity of each fraction was assessed by a Hoechst staining-based apoptosis assay using malignant melanoma MeWo cells. By these repeated approaches through chromatographic segregation and cell biological assay, we finally succeeded in identifying the target substance from a certain fraction that included neutral hydrophilic components using a pre-column and post-column chlorine adduct ionization LC APCI MS method. The target substance was a mono-carbohydrate, xylitol, that induced apoptotic cell death in MeWo cells but not in normal human OUMS-24 fibroblasts. This is the first study showing that Cordyceps militaris extract contains a large amount of xylitol. Thus, our results will contribute greatly to uncovering the mysterious multifunctional herbal drug Cordyceps militaris as an anti-tumor agent.

Link information
DOI
https://doi.org/10.1016/j.jchromb.2017.07.022
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28750234
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000411542000029&DestApp=WOS_CPL
ID information
  • DOI : 10.1016/j.jchromb.2017.07.022
  • ISSN : 1570-0232
  • eISSN : 1873-376X
  • Pubmed ID : 28750234
  • Web of Science ID : WOS:000411542000029

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