BPIFB1 (LPLUNC1) inhibits migration and invasion of nasopharyngeal carcinoma by interacting with VTN and VIM

Br J Cancer. 2018 Jan;118(2):233-247. doi: 10.1038/bjc.2017.385. Epub 2017 Nov 9.

Abstract

Background: Bactericidal/Permeability-increasing-fold-containing family B member 1 (BPIFB1, previously termed LPLUNC1) is highly expressed in the nasopharynx, significantly downregulated in nasopharyngeal carcinoma (NPC), and associated with prognosis in NPC patients. Because metastasis represents the primary cause of NPC-related death, we explored the role of BPIFB1 in NPC migration and invasion.

Methods: The role of BPIFB1 in NPC metastasis was investigated in vitro and in vivo. A co-immunoprecipitation assay coupled with mass spectrometry was used to identify BPIFB1-binding proteins. Additionally, western blotting, immunofluorescence, and immunohistochemistry allowed assessment of the molecular mechanisms associated with BPIFB1-specific metastatic inhibition via vitronectin (VTN) and vimentin (VIM) interactions.

Results: Our results showed that BPIFB1 expression markedly inhibited NPC cell migration, invasion, and lung-metastatic abilities. Additionally, identification of two BPIFB1-interacting proteins, VTN and VIM, showed that BPIFB1 reduced VTN expression and the formation of a VTN-integrin αV complex in NPC cells, leading to inhibition of the FAK/Src/ERK signalling pathway. Moreover, BPIFB1 attenuated NPC cell migration and invasion by inhibiting VTN- or VIM-induced epithelial-mesenchymal transition.

Conclusions: This study represents the first demonstration of BPIFB1 function in NPC migration, invasion, and lung metastasis. Our findings indicate that re-expression of BPIFB1 might represent a useful strategy for preventing and treating NPC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoantigens / biosynthesis
  • Autoantigens / metabolism*
  • Cell Line, Tumor
  • Cell Movement / physiology
  • Fatty Acid-Binding Proteins
  • Focal Adhesion Kinase 1 / metabolism
  • Humans
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / secondary
  • MAP Kinase Signaling System
  • Male
  • Mice
  • Mice, Nude
  • Nasopharyngeal Carcinoma / metabolism*
  • Nasopharyngeal Carcinoma / pathology
  • Nasopharyngeal Neoplasms / metabolism*
  • Nasopharyngeal Neoplasms / pathology
  • Neoplasm Invasiveness
  • Proteins / metabolism*
  • Vimentin / antagonists & inhibitors
  • Vimentin / biosynthesis
  • Vimentin / metabolism*
  • Vitronectin / antagonists & inhibitors
  • Vitronectin / biosynthesis
  • Vitronectin / metabolism*
  • src-Family Kinases / metabolism

Substances

  • Autoantigens
  • BPIFB1 protein, human
  • Fatty Acid-Binding Proteins
  • Proteins
  • Vimentin
  • Vitronectin
  • Focal Adhesion Kinase 1
  • PTK2 protein, human
  • src-Family Kinases