Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Cytotoxic dammarane glycosides from processed ginseng.

Il Ho Park1, Long Zhu Piao, Sung Won Kwon

  • 1College of Pharmacy, Seoul National University, South Korea.

Chemical & Pharmaceutical Bulletin
|April 20, 2002
PubMed
Summary

High-temperature steamed ginseng exhibits enhanced cytotoxicity against hepatoma cancer cells. Specific ginsenosides were identified as active compounds, showing greater potency than cisplatin.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Extracellular vesicles from steatotic hepatocytes promote endothelial dysfunction and atherogenesis via miR-30b-5p/ELOVL5 axis.

Molecular therapy : the journal of the American Society of Gene Therapy·2026
Same author

Neuroprotective effects of quercetin in animal models of neurodegenerative diseases: A systematic review and meta-analysis.

Journal of the science of food and agriculture·2026
Same author

Lipidomic analysis of bile from patients with extrahepatic cholangiocarcinoma.

PloS one·2026
Same author

LncRNA Wee1-AS coordinates oxidative fatty acid metabolism through the activation of mitochondrial CDK1/CYCLIN B1.

Signal transduction and targeted therapy·2026
Same author

Neuroeconomic adaptation to norm shifts is preserved in borderline personality disorder.

Acta neuropsychiatrica·2026
Same author

TMEM120A maintains adipose tissue lipid homeostasis through ER CoA channeling.

Nature communications·2025

Area of Science:

  • Pharmacology
  • Natural Products Chemistry
  • Cancer Biology

Background:

  • Ginseng (Panax ginseng) is a traditional medicinal herb with known therapeutic properties.
  • High-temperature processing, such as steaming, can alter the chemical composition and biological activity of ginseng.
  • Hepatocellular carcinoma (HCC) remains a significant global health challenge, necessitating novel therapeutic strategies.

Purpose of the Study:

  • To investigate the effect of high-temperature steaming on the cytotoxicity of ginseng.
  • To identify the specific active ginsenosides responsible for the enhanced anti-cancer effects.
  • To compare the efficacy of these active compounds with a standard chemotherapeutic agent, cisplatin.

Main Methods:

  • High-temperature steaming of ginseng followed by extraction.

Related Experiment Videos

  • High-Performance Liquid Chromatography (HPLC) for separation and fractionation of ginseng extracts.
  • Methyl Thiazolyl Tetrazolium (MTT) assay to determine cytotoxicity against SK-Hep-1 hepatoma cancer cells.
  • Main Results:

    • High-temperature steamed ginseng demonstrated increased cytotoxicity towards SK-Hep-1 cells compared to unsteamed ginseng.
    • HPLC analysis identified ginsenosides Rg3, Rg5, Rk1, Rs5, and Rs4 as the primary active compounds.
    • The 50% growth inhibition (GI50) values for these ginsenosides ranged from 11 to 41 microM.
    • Cisplatin, a control drug, exhibited a GI50 of 84 microM under the same experimental conditions, indicating higher potency of the identified ginsenosides.

    Conclusions:

    • High-temperature steaming significantly enhances the cytotoxic activity of ginseng against hepatoma cancer cells.
    • Specific ginsenosides (Rg3, Rg5, Rk1, Rs5, Rs4) are key contributors to this enhanced anti-cancer effect.
    • These identified ginsenosides represent promising natural compounds for further development as potential therapeutic agents for hepatocellular carcinoma, showing superior efficacy to cisplatin in this model.