MGr1-Ag promotes invasion and bone metastasis of small-cell lung cancer in vitro and in vivo

Oncol Rep. 2013 Jun;29(6):2283-90. doi: 10.3892/or.2013.2396. Epub 2013 Apr 9.

Abstract

Bone metastasis of small-cell lung cancer (SCLC) usually occurs early in the progression of the disease. However, the molecular mechanism underlying bone metastasis is largely unknown. MGr1-Ag, a multifunction protein, has been suggested to play important roles in cell growth, differentiation and migration. In our present study, MGr1-Ag was found to be highly expressed in bone-metastatic SCLC cells (SBC-5 cell line) as compared with the expression in cells without bone-metastatic ability (SBC-3 cell line). Therefore, we hypothesized that MGr1-Ag is involved in bone metastasis of SCLC. Using a sense vector to upregulate MGr1-Ag expression in SBC-3 cells, we found that forced overexpression of MGr1-Ag enhanced cell invasion and migration in vitro and promoted bone metastases in vivo. Furthermore, specific siRNA-induced knockdown of MGr1-Ag expression in SBC-5 cells suppressed the potential of cell invasion and migration in vitro and dramatically decreased the number and sites of bone metastasis in vivo. We also found that MGr1-Ag induced SCLC cells to undergo epithelial-mesenchymal transition (EMT), as demonstrated by cell morphological changes, decreased expression of epithelial markers and increased expression of mesenchymal markers. Taken together, we conclude that MGr1-Ag promotes SCLC cell invasion and bone metastasis in vitro and in vivo, and that this is partially mediated via the EMT pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism*
  • Bone Neoplasms / metabolism*
  • Bone Neoplasms / secondary
  • Cadherins / metabolism
  • Cell Line, Tumor
  • Cell Movement
  • Cell Shape
  • Epithelial-Mesenchymal Transition
  • Female
  • Fibronectins / metabolism
  • Gene Expression
  • Gene Knockdown Techniques
  • Humans
  • Lung Neoplasms / metabolism*
  • Lung Neoplasms / pathology
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Neoplasm Invasiveness
  • Neoplasm Transplantation
  • RNA, Small Interfering / genetics
  • Small Cell Lung Carcinoma / metabolism*
  • Small Cell Lung Carcinoma / secondary
  • Up-Regulation

Substances

  • Antigens, CD
  • Antigens, Neoplasm
  • CDH1 protein, human
  • Cadherins
  • Fibronectins
  • MGr1-antigen, human
  • RNA, Small Interfering