The Novel Nutraceutical KJS018A Prevents Hepatocarcinogenesis Promoted by Inflammation

Do Luong Huynh1, Nisansala Chandimali1, Jiao Jiao Zhang1

  • 1Laboratory of Animal Genetic Engineering and Stem Cell Biology, Advanced Convergence Technology & Science, Jeju National University, Jeju 63243, Republic of Korea.

Insights

This study shows the herbal mixture KJS018A inhibits liver cancer development and inflammation. KJS018A reduces cancer cell growth, metastasis, and key inflammatory markers like Interleukin-6 (IL-6) and Cyclooxygenase-2 (Cox-2).

Area of Science:

  • Oncology
  • Inflammation research
  • Pharmacology

Background:

  • Inflammation is linked to cancer initiation and progression.
  • Cyclooxygenase-2 (Cox-2) plays a significant role in inflammation and tumor development.
  • The herbal mixture KJS018A is derived from plants with known anti-cancer and anti-inflammatory properties.

Purpose of the Study:

  • To investigate the inhibitory effects of KJS018A on liver cancer (hepatocarcinogenesis) and inflammation.
  • To understand the molecular mechanisms underlying KJS018A's action.

Main Methods:

  • Assessing KJS018A's impact on hepatic malignant cell proliferation.
  • Measuring levels of Interleukin-6 (IL-6) and Cyclooxygenase-2 (Cox-2).
  • Evaluating the modulation of the IL-6/STAT3/Cox-2 pathway and epithelial-mesenchymal transition markers (Twist, N-cadherin, MMP-9, E-cadherin).
  • Utilizing immunohistochemistry to analyze tumor growth and marker expression in vivo.

Main Results:

  • KJS018A significantly inhibited hepatic malignant cell proliferation.
  • KJS018A downregulated IL-6 and Cox-2 levels, and diminished the inflammatory effects of PMA.
  • The mixture suppressed cancer cell metastasis by altering key protein expressions and reduced tumor growth.
  • KJS018A also reduced IL-6 and Cox-2 levels in tumor tissues.

Conclusions:

  • KJS018A demonstrates significant anti-cancer and anti-inflammatory effects.
  • The herbal mixture acts through the IL-6/STAT3/Cox-2 pathway and influences epithelial-mesenchymal transition.
  • KJS018A shows potential for preventing inflammation-driven liver cancer.

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