Cellular reprogramming and signaling control by kaempferol in colorectal cancer

Bo Wu1, Li-Li Qiu2, Yuan Bu3

  • 1Health College, Binzhou Polytechnic University, Binzhou, 256603, Shandong, China.

Discover Oncology
|July 13, 2026
PubMed

Insights

Kaempferol (KMP), a natural compound, shows promise in treating colorectal cancer (CRC) by inhibiting tumor growth and proliferation. However, its clinical use is limited by poor bioavailability, suggesting nano-delivery systems could enhance its therapeutic potential.

Area of Science:

  • Oncology
  • Pharmacology
  • Natural Products Chemistry

Background:

  • Colorectal cancer (CRC) presents significant therapeutic challenges due to drug resistance and toxicity.
  • Kaempferol (KMP), a natural flavonoid, exhibits low toxicity and diverse biological activities, including anti-inflammatory, antioxidant, anti-angiogenic, and apoptosis-inducing effects.
  • KMP has demonstrated potential in preclinical studies for various diseases, including cancer therapy.

Purpose of the Study:

  • To review the anticancer effects and mechanisms of Kaempferol (KMP) in colorectal cancer (CRC) therapy.
  • To explore the potential of KMP as a therapeutic agent and sensitizer in CRC treatment.
  • To discuss the limitations of KMP, such as poor bioavailability, and the potential of nano-based delivery systems.

Main Methods:

  • Literature review of studies investigating Kaempferol's role in colorectal cancer.
  • Analysis of KMP's effects on CRC cell proliferation, tumor growth, and colitis-CRC progression.
  • Examination of signaling pathways modulated by KMP, including MMPs, VEGF/VEGFR, Wnt/β-catenin, and PI3K/Akt/mTOR.

Main Results:

  • KMP inhibits CRC cell proliferation and tumor growth.
  • KMP can prevent the progression of colitis to CRC.
  • KMP modulates multiple cancer-related signaling pathways, acting as a multi-targeted inhibitor.

Conclusions:

  • Kaempferol (KMP) is a promising natural compound for colorectal cancer (CRC) therapy due to its multi-targeted anticancer effects.
  • KMP's clinical application is hindered by poor stability, absorption, and bioavailability.
  • Nano-based delivery systems offer a potential strategy to overcome KMP's limitations and enhance its therapeutic efficacy in CRC treatment.

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