Black ginseng extract suppresses lung cancer growth in a xenograft mouse model

Hye Jin Park1, Ha Rin Namkung2, Su Bin Jung2

  • 1Truth & Ginseng Biotechnology Research Co., Ltd., Jinan, Republic of Korea.

Abstract

Insights

Black ginseng extract (BGE) effectively reduced lung cancer cell proliferation and tumor growth in mice. This natural compound demonstrated significant antitumor effects with no observable toxicity in major organs, suggesting its potential as a lung cancer therapeutic.

Area of Science:

  • Oncology
  • Natural Products Chemistry
  • Pharmacology

Background:

  • Lung cancer is a leading cause of cancer mortality, with current treatments facing limitations due to toxicity and drug resistance.
  • Ginsenosides from natural products, particularly black ginseng extract (BGE), exhibit anticancer properties, but their specific impact on lung cancer requires further investigation.
  • The study aimed to explore the preventive and therapeutic potential of BGE against human lung cancer cells and tumor growth in vivo.

Purpose of the Study:

  • To evaluate the cytotoxic and apoptotic effects of BGE on human lung cancer cell lines (Calu-3 and NCI-H1975) in vitro.
  • To assess the efficacy of BGE in inhibiting the growth of lung cancer xenografts in mice.
  • To determine the safety profile of BGE by examining its effects on major organs.

Main Methods:

  • In vitro cytotoxicity and apoptosis assays were performed on Calu-3 and NCI-H1975 lung cancer cells treated with BGE.
  • In vivo studies involved administering BGE orally to athymic mice bearing Calu-3 lung tumor xenografts.
  • Tumor volume, body weight, and organ histology (liver, spleen) were analyzed to assess efficacy and toxicity.

Main Results:

  • BGE induced significant apoptosis-associated cytotoxicity in both Calu-3 (10 mg/mL) and NCI-H1975 (0.5 mg/mL) cells.
  • In vivo, BGE treatment significantly reduced lung tumor weight and size without affecting body weight.
  • Histopathological examination revealed no BGE-induced abnormalities in the liver or spleen, indicating a lack of organ toxicity.

Conclusions:

  • BGE exhibits potent antitumor activity against lung cancer cells in vitro and inhibits tumor growth in vivo.
  • BGE demonstrates a favorable safety profile, with no detectable toxicity in key organs.
  • These findings support the potential of BGE as a safe and effective agent for lung cancer prevention or therapy.

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