Allicin Could Potentially Alleviate Oral Cancer Pain by Inhibiting "Pain Mediators" TNF-alpha, IL-8, and Endothelin

Curr Issues Mol Biol. 2021 May 23;43(1):187-196. doi: 10.3390/cimb43010016.

Abstract

To evaluate the effects of allicin on mediators of pain secreted by oral cancer cells in vitro, single-cell suspensions were prepared by enzymatic method from oral squamous cell carcinoma (OSCC). Cancer stem cells were isolated by the CD133+ selection method with magnetic cell sorting. Stemness markers were checked in both cancer cells and cancer stem cells by RT-PCR. Comparative analysis of pain mediators TNF-alpha, IL-8, and endothelin at both RNA and protein levels for normal epithelial cells, cancer cells, and cancer stem cells was carried out with and without allicin treatment. CD133 and CD44 expression levels were checked in cancer cells and cancer stem cells flow cytometrically. Allicin inhibited both gene and protein expression of TNF-alpha, IL-8, and endothelin in both cancer cells and cancer stem cells. Allicin is more likely to be a promising treatment in alleviating the levels of pain and inflammation in OSCCs.

Keywords: allicin; cancer stem cells; oral cancer; pain.

MeSH terms

  • AC133 Antigen / metabolism
  • Antioxidants / pharmacology
  • Cancer Pain / drug therapy*
  • Cancer Pain / etiology
  • Cancer Pain / metabolism
  • Cancer Pain / pathology
  • Disulfides / pharmacology*
  • Endothelins / antagonists & inhibitors*
  • Humans
  • Interleukin-8 / antagonists & inhibitors*
  • Mouth Neoplasms / drug therapy
  • Mouth Neoplasms / pathology
  • Mouth Neoplasms / physiopathology*
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Primary Cell Culture
  • Sulfinic Acids / pharmacology*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors*

Substances

  • AC133 Antigen
  • Antioxidants
  • CXCL8 protein, human
  • Disulfides
  • Endothelins
  • Interleukin-8
  • Sulfinic Acids
  • TNF protein, human
  • Tumor Necrosis Factor-alpha
  • allicin