Caffeic acid inhibits the tumorigenicity of triple-negative breast cancer cells through the FOXO1/FIS pathway

Biomed Pharmacother. 2024 Sep:178:117158. doi: 10.1016/j.biopha.2024.117158. Epub 2024 Jul 22.

Abstract

Triple-negative breast cancer (TNBC) still one of the most challenging sub-type in breast cancer clinical. Caffeic acid (CA) derived from effective components of traditional Chinese herbal medicine has been show potential against TNBCs. Our research has found that CA can inhibit the proliferation of TNBC cells while also suppressing the size of cancer stem cell spheres. Additionally, it reduces reactive oxygen species (ROS) levels and disruption of mitochondrial membrane potential. Simultaneously, CA influences the stemness of TNBC cells by reducing the expression of the stem cell marker protein CD44. Furthermore, we have observed that CA can modulate the FOXO1/FIS signaling pathway, disrupting mitochondrial function, inducing mitochondrial autophagy, and exerting anti-tumor activity. Additionally, changes in the immune microenvironment were detected using a mass cytometer, we found that CA can induce M1 polarization of macrophages, enhancing anti-tumor immune responses to exert anti-tumor activity. In summary, CA can be considered as a lead compound for further research in targeting TNBC.

Keywords: Caffeic acid; FOXO1/FIS; Triple-negative breast cancer; mitochondrial autophagy; stemness; tumor microenvironment.

MeSH terms

  • Animals
  • Autophagy / drug effects
  • Caffeic Acids* / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation* / drug effects
  • Female
  • Forkhead Box Protein O1 / metabolism
  • Humans
  • Membrane Potential, Mitochondrial / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Reactive Oxygen Species / metabolism
  • Signal Transduction* / drug effects
  • Triple Negative Breast Neoplasms* / drug therapy
  • Triple Negative Breast Neoplasms* / metabolism
  • Triple Negative Breast Neoplasms* / pathology
  • Tumor Microenvironment / drug effects

Substances

  • caffeic acid
  • Caffeic Acids
  • Forkhead Box Protein O1
  • FOXO1 protein, human
  • Reactive Oxygen Species