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Lychee Seed Extract Targets Proliferation, Differentiation, and Cell Cycle Proteins to Suppress Human Colorectal
Szu-Nian Yang1,2, Yi-Ping Chang3,4, Oscar C Y Yang5
1Department of Psychiatry, Taipei Veterans General Hospital, Taoyuan Branch, Taoyuan 330023, Taiwan.
Abstract:
Colorectal cancer (CRC) remains a leading global health challenge, and natural products are increasingly explored for their multi-targeted therapeutic potential. Litchi chinensis seed extract (LCSE) has shown promising anti-cancer activity in vitro, though its in vivo effects remain underexplored. LCSE was analyzed by colorimetric assays and HPLC to quantify the phytochemical composition. Nude mice bearing HT-29 or SW480 xenografts were orally administered LCSE (0.1 or 0.6 g/kg) daily for 14 days. Tumor volume was measured, and immunohistochemistry was used to assess EGFR, p21, p53, Ki-67, CEA, CK20, CDX2, and Bax expression. Phytochemical profiling demonstrated LCSE contains abundant phenolics and flavonoids, with gallic acid as a predominant constituent, underscoring the potential bioactive properties. LCSE significantly inhibited tumor growth in HT-29 xenografts and dose-dependently reduced EGFR, p21, p53, cell cycle proteins and proliferation/differentiation markers. In SW480 tumors, inhibitory effects were evident primarily at the higher dose, with limited reduction in p53 expression. Bax levels remained unchanged in both models, indicating a non-apoptotic mechanism. No systemic toxicity was observed in treated mice. LCSE exhibits dose-dependent anti-tumor activity in CRC xenografts, likely mediated through suppression of proliferation and modulation of key regulatory proteins rather than apoptosis. These findings support LCSE as a safe, multi-target botanical candidate for CRC intervention and justify further mechanistic and translational studies.
Insights
Litchi chinensis seed extract (LCSE) shows anti-cancer effects against colorectal cancer (CRC) in vivo. LCSE inhibits tumor growth by reducing cell proliferation and modulating key proteins, offering a safe botanical option for CRC intervention.
Area of Science:
- Oncology
- Pharmacology
- Natural Products Chemistry
Background:
- Colorectal cancer (CRC) is a major global health concern.
- Natural products are being investigated for their multi-targeted anti-cancer properties.
- Litchi chinensis seed extract (LCSE) demonstrates in vitro anti-cancer activity, but in vivo efficacy is largely unexplored.
Purpose of the Study:
- To evaluate the in vivo anti-tumor effects of LCSE in colorectal cancer xenograft models.
- To investigate the phytochemical composition of LCSE.
- To assess the impact of LCSE on tumor growth, proliferation, and key protein expression.
Main Methods:
- Phytochemical analysis of LCSE using colorimetric assays and HPLC.
- Administration of LCSE to nude mice with HT-29 or SW480 xenografts.
- Measurement of tumor volume and analysis of protein expression (EGFR, p21, p53, Ki-67, Bax) via immunohistochemistry.
Main Results:
- LCSE contains significant amounts of phenolics and flavonoids, with gallic acid as a primary component.
- LCSE significantly inhibited tumor growth in HT-29 xenografts and dose-dependently reduced EGFR, p21, p53, and proliferation markers.
- In SW480 xenografts, inhibition was observed at higher doses, with minimal impact on p53 and no change in Bax, suggesting a non-apoptotic mechanism. No toxicity was noted.
Conclusions:
- LCSE exhibits dose-dependent anti-tumor activity in CRC xenografts, primarily by suppressing proliferation and modulating regulatory proteins.
- The mechanism appears to involve pathways other than apoptosis.
- LCSE is a safe, multi-target botanical agent with potential for CRC intervention, warranting further research.
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