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Updated: Jan 20, 2026

Orthotopic Mouse Model of Colorectal Cancer
Published on: December 4, 2007
Korean Red Ginseng Extract Increases Apoptosis by Activation of the Noxa Pathway in Colorectal Cancer
Yoon A Jeong1, Bo Ram Kim2, Dae Young Kim1
1Graduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Background:
Although the anticancer activity of Korean Red Ginseng (KRG) has been known in various cancers, the mechanism of KRG-induced apoptosis is unknown in colorectal cancer (CRC). In our study, we examined whether KRG induces apoptosis in CRC cells.
Methods:
In the cell viability assay, the concentration of the appropriate KRG extracts was fixed at 2.5 mg/mL in numerous CRC cells. This fixed concentration was in other experiments, and it was confirmed that the KRG extracts induce apoptosis in CRC cells.
Results:
We found that KRG induced Noxa activation and apoptosis and increased endoplasmic reticulum stress via reactive oxygen species production. This indicated that KRG efficiently enhanced cell death in CRC cells.
Conclusion:
Our results show that KRG can be used as a possible anticancer drug for patients with CRC.
Insights
Korean Red Ginseng (KRG) effectively triggers apoptosis and endoplasmic reticulum stress in colorectal cancer (CRC) cells. These findings suggest KRG holds potential as an anticancer drug for CRC patients.
Area of Science:
- Oncology
- Pharmacology
- Cell Biology
Background:
- The anticancer properties of Korean Red Ginseng (KRG) are documented across several cancer types.
- The specific mechanisms underlying KRG-induced apoptosis in colorectal cancer (CRC) remain largely uncharacterized.
Purpose of the Study:
- This study aimed to investigate whether KRG can induce apoptosis in colorectal cancer (CRC) cells.
- To elucidate the molecular pathways involved in KRG's effect on CRC.
Main Methods:
- Cell viability assays were performed on multiple CRC cell lines.
- KRG extracts were used at a fixed concentration of 2.5 mg/mL.
- Apoptosis induction by KRG in CRC cells was confirmed through various experimental assays.
Main Results:
- KRG treatment led to the activation of Noxa, a key protein in apoptosis.
- Increased endoplasmic reticulum stress was observed, mediated by reactive oxygen species (ROS) production.
- KRG demonstrated efficient enhancement of cell death in CRC cells.
Conclusions:
- The findings indicate that KRG effectively induces apoptosis and endoplasmic reticulum stress in CRC cells.
- KRG shows promise as a potential therapeutic agent for colorectal cancer.
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