Ganoderma lucidum Extract Reduces the Motility of Breast Cancer Cells Mediated by the RAC⁻Lamellipodin Axis

Nutrients. 2019 May 19;11(5):1116. doi: 10.3390/nu11051116.

Abstract

Breast cancer (BC) is the second leading cause of cancer death among women worldwide. The main cause of BC morbidity and mortality is the invasiveness capacity of cancer cells that may lead to metastasis. Here, we aimed to investigate the therapeutic efficacy of Ganoderma lucidum extract (GLE)-a medicinal mushroom with anticancer properties-on BC motility via the Rac/Lamellipodin pathway. GLE treatment effects were tested on MDA-MB-231 breast cancer cells. The effects were tested on cell viability, migration and invasion. Pulldowns, immunoblotting, and immunofluorescence were used to measure Rac activity and the expression of proteins involved in cell migration and in lamellipodia formation, respectively. As a result, GLE suppressed BC cell viability, migration, and invasion capacity. GLE impaired Rac activity, as well as downregulated Lamellipodin, ENA/VASP, p-FAK (Tyr925), Cdc42, and c-Myc expression. Lamellipodia formation was significantly reduced by GLE. In conclusion, we demonstrate that GLE reduces Rac activity and downregulates signaling molecules involved in lamellipodia formation. These novel findings serve as basis for further studies to elucidate the potential of GLE as a therapeutic agent regulating the Rac/Lamellipodin pathway in BC metastasis.

Keywords: Ganoderma lucidum; Rac; breast cancer; cancer cell migration; lamellipodin.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Biological Products / pharmacology
  • Biological Products / therapeutic use*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / therapy*
  • Carrier Proteins / metabolism*
  • Cell Line, Tumor
  • Cell Movement / drug effects*
  • Cell Survival / drug effects
  • DNA-Binding Proteins / metabolism
  • Down-Regulation
  • Female
  • Humans
  • Membrane Proteins / metabolism*
  • Neoplasm Invasiveness / prevention & control
  • Proto-Oncogene Proteins c-myc / metabolism
  • Pseudopodia / drug effects
  • Reishi*
  • Signal Transduction
  • rac GTP-Binding Proteins / metabolism*

Substances

  • Antineoplastic Agents
  • Biological Products
  • Carrier Proteins
  • DNA-Binding Proteins
  • ENA-VASP proteins
  • MYC protein, human
  • Membrane Proteins
  • Proto-Oncogene Proteins c-myc
  • RAPH1 protein, human
  • rac GTP-Binding Proteins