Effects of Oplopanax horridus on human colorectal cancer cells

Xiao-Li Li1, Shi Sun, Guang-Jian Du

  • 1Tang Center for Herbal Medicine Research, and Department of Anesthesia & Critical Care, Pritzker School of Medicine, University of Chicago, Chicago, IL 60637, USA.

Anticancer Research
|March 25, 2010
PubMed
Abstract

Insights

Oplopanax horridus extract (OhE) and its fractions OhF4 and OhF5 show antiproliferative effects against human colorectal cancer cells. These compounds induce apoptosis and regulate cell cycle transition, suggesting potential as anticancer agents.

Area of Science:

  • Pharmacology
  • Cancer Biology
  • Natural Products Chemistry

Background:

  • Colorectal cancer (CRC) remains a leading cause of cancer-related mortality worldwide.
  • There is a continuous need for novel therapeutic strategies, including those derived from natural sources.
  • Oplopanax horridus (devil's club) is a plant with traditional medicinal uses.

Purpose of the Study:

  • To investigate the antiproliferative effects of Oplopanax horridus extract (OhE) and its fractions (OhF1-OhF5) on human colorectal cancer cell lines.
  • To elucidate the underlying mechanisms of action, including induction of apoptosis and cell cycle regulation.

Main Methods:

  • Human colorectal cancer cell lines (HCT-116, SW-480, HT-29) were treated with OhE and its fractions.
  • Cell proliferation was assessed using the MTS assay.
  • Apoptosis and cell cycle distribution were analyzed by flow cytometry.

Main Results:

  • OhE, OhF4, and OhF5 significantly inhibited the proliferation of HCT-116, SW-480, and HT-29 cells.
  • OhF4 demonstrated the most potent growth inhibition.
  • OhE, OhF4, and OhF5 induced apoptosis and caused a G2/M phase cell cycle arrest in a dose- and time-dependent manner.

Conclusions:

  • Oplopanax horridus extract possesses significant antiproliferative activity against human colorectal cancer cells.
  • The active compounds are concentrated in the OhF4 and OhF5 fractions.
  • The anticancer effects are mediated through the induction of apoptosis and regulation of cell cycle progression.

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