Effects of Antarctic krill docosahexaenoic acid on MCF-7 cell migration and invasion induced by the interaction of CD95 with caveolin-1

Life Sci. 2018 Jan 1:192:270-277. doi: 10.1016/j.lfs.2017.11.011. Epub 2017 Nov 9.

Abstract

Tumor metastasis leads to a poor prognosis in breast cancer, yet the mechanisms remain unclear. Docosahexaenoic acid (DHA) extracted from Antarctic krill is an optical isomer of common DHA and has a much stronger anti-neoplastic effect. In this work, the migration and invasion abilities of MCF-7 cells treated with low concentrations of Antarctic krill DHA were evaluated. Low concentrations of Antarctic krill DHA significantly reduced the numbers of migrating and invasive MCF-7 cells, whereas the cell numbers decreased slowly in the CD95-silenced MCF-7 cells, which implies that CD95 might be involved in cell migration and invasion. Additionally, co-immunoprecipitation and Western blotting demonstrated that Antarctic krill DHA induced the accumulation of CD95 and caveolin-1 interaction, resulting in the down-regulation of MMP2 expression through the FAK/SRC/PI3K/AKT signaling pathway. In conclusion, Antarctic krill DHA enhanced the interaction between CD95 and caveolin-1, which may led to an inhibitory effect on cell migration and invasion via the FAK/SRC/PI3K/AKT signaling pathway. Our study indicates that Antarctic krill DHA has great potential for tumor therapy and has revealed a new metastatic mechanism mediated by the interaction of CD95 with caveolin-1.

Keywords: Antarctic krill; CD95; Caveolin-1; DHA; Invasion; Migration.

MeSH terms

  • Animals
  • Antarctic Regions
  • Caveolin 1 / drug effects*
  • Cell Count
  • Cell Movement / drug effects*
  • Cell Survival
  • Docosahexaenoic Acids / pharmacology*
  • Euphausiacea / chemistry*
  • Female
  • Humans
  • MCF-7 Cells
  • Matrix Metalloproteinase 2 / biosynthesis
  • Matrix Metalloproteinase 2 / genetics
  • Neoplasm Invasiveness*
  • Neoplasm Metastasis
  • Signal Transduction / drug effects
  • fas Receptor / drug effects*

Substances

  • CAV1 protein, human
  • Caveolin 1
  • FAS protein, human
  • fas Receptor
  • Docosahexaenoic Acids
  • MMP2 protein, human
  • Matrix Metalloproteinase 2