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Updated: May 9, 2025

In vitro Organoid Culture of Primary Mouse Colon Tumors
Published on: May 17, 2013
SH003 Inhibits Proliferation and Induces Apoptosis in Colon Cancer Through the RTK-STAT3 Pathway
Hyun-Ha Hwang1, Ji-Sung Yoo1, Jeong-Hui Je1
1Department of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
SH003, an herbal mixture, effectively combats colon cancer by inducing apoptosis and cell cycle arrest. This promising treatment demonstrated significant tumor growth inhibition in vivo with no observed systemic toxicity.
Area of Science:
- Oncology
- Pharmacology
- Herbal Medicine
Background:
- Colon cancer presents high incidence and mortality, necessitating novel therapeutic strategies beyond chemotherapy.
- Existing treatments offer limited survival benefits for advanced colon cancer.
- SH003, a herbal mixture, shows potential anticancer properties.
Purpose of the Study:
- To investigate the anticancer effects of SH003 on colon cancer cell lines.
- To evaluate the efficacy and safety of SH003 in a colon cancer xenograft mouse model.
- To explore the molecular mechanisms underlying SH003's anti-colon cancer activity.
Main Methods:
- In vitro: Assessed cell viability, apoptosis, cell cycle progression, and RTK-STAT3 pathway disruption in human colon cancer cell lines.
- In vivo: Utilized an HCT116 xenograft mouse model to evaluate tumor growth inhibition and systemic toxicity.
- Analyzed key proteins involved in apoptosis, cell cycle regulation, and the RTK-STAT3 pathway.
Main Results:
- SH003 exhibited time-dependent cytotoxicity across multiple colon cancer cell lines.
- Confirmed apoptosis induction via increased cleaved PARP and caspase levels.
- Observed G1/S phase cell cycle arrest and disruption of the RTK-STAT3 pathway (reduced ALK and STAT3 phosphorylation).
- SH003 significantly inhibited tumor growth in vivo without significant systemic toxicity.
Conclusions:
- SH003 demonstrates potent anticancer effects against colon cancer through apoptosis induction, cell cycle arrest, and RTK-STAT3 pathway inhibition.
- In vivo studies validate SH003's efficacy and safety as a potential therapeutic agent for colon cancer.
- Further research is recommended to fully elucidate SH003's mechanisms and clinical potential.
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