Ophiopogonin D suppresses TGF-β1-mediated metastatic behavior of MDA-MB-231 breast carcinoma cells via regulating ITGB1/FAK/Src/AKT/β-catenin/MMP-9 signaling axis

Toxicol In Vitro. 2020 Dec:69:104973. doi: 10.1016/j.tiv.2020.104973. Epub 2020 Aug 18.

Abstract

Ophiopogonin D, a steroidal glycoside extracted from the Traditional Chinese Medicine Ophiopogon japonicus, shows anti-tumor property in several lines of cancers; however, its effect on triple-negative breast cancer (TNBC) has not been investigated. In this study, the anti-metastatic effect of Ophiopogonin D in TNBC cells as well as the underlying mechanism in such process was explored. Ophiopogonin D dose-dependently decreased cell proliferation of MDA-MB-231 cells. Meanwhile, Ophiopogonin D significantly inhibited TGF-β1-induced metastatic behavior of MDA-MB-231 cells, including EMT, anoikis resistance as well as migration and invasion, via suppressing MMP-9 activity. Mechanically, Ophiopogonin D achieved its effect through efficiently abolishing ITGB1 expression, thus reducing the phosphorylation of FAK, Src and AKT, as well as upregulating nuclear β-catenin. ITGB1 overexpression partly recovered Ophiopogonin D's inhibitory effect on metastatic behavior via activating MMP-9. These results demonstrated that Ophiopogonin D could suppress TGF-β1-mediated metastatic behavior of MDA-MB-231 cells by regulating ITGB1/FAK/Src/AKT/β-catenin/MMP-9 signaling axis, which might provide new insight for the control of TNBC metastasis.

Keywords: ITGB1/FAK/Src/AKT/β-catenin/MMP-9 signaling axis; Metastastic behavior; Ophiopogonin D; Triple-negative breast cancer.

MeSH terms

  • Anoikis / drug effects
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Survival / drug effects
  • Female
  • Focal Adhesion Kinase 1 / metabolism
  • Humans
  • Integrin beta1 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Saponins / pharmacology*
  • Signal Transduction / drug effects
  • Spirostans / pharmacology*
  • Transforming Growth Factor beta1 / metabolism
  • Triple Negative Breast Neoplasms* / drug therapy
  • Triple Negative Breast Neoplasms* / metabolism
  • Triple Negative Breast Neoplasms* / pathology
  • Wound Healing / drug effects
  • beta Catenin / metabolism
  • src-Family Kinases / metabolism

Substances

  • Antineoplastic Agents
  • CTNNB1 protein, human
  • Integrin beta1
  • Itgb1 protein, human
  • Saponins
  • Spirostans
  • TGFB1 protein, human
  • Transforming Growth Factor beta1
  • beta Catenin
  • ophiopogonin D
  • Focal Adhesion Kinase 1
  • PTK2 protein, human
  • src-Family Kinases
  • Proto-Oncogene Proteins c-akt
  • MMP9 protein, human
  • Matrix Metalloproteinase 9