CEACAM6 promotes tumor migration, invasion, and metastasis in gastric cancer

Acta Biochim Biophys Sin (Shanghai). 2014 Apr;46(4):283-90. doi: 10.1093/abbs/gmu001. Epub 2014 Feb 3.

Abstract

Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) shows increased expression in a wide variety of human cancers, and its over-expression is associated with enhanced migration, invasion, and in vivo metastasis. Here, we reported that CEACAM6 was up-regulated in gastric cancer (GC) cell lines and tumor tissues. Over-expression of CEACAM6 in MKN-45 and SGC-7901 GC cells promoted migration and invasion in vitro and metastasis in athymic mice, whereas migration and invasion of MKN-28 and SNU-16 GC cells were suppressed by knockdown of CEACAM6. We also observed that steroid receptor coactivator (C-SRC) phosphorylation was increased when CEACAM6 was over-expressed in SGC-7901 cells. Taken together, these results suggested that CEACAM6 functions as an oncoprotein in GC and may be an important metastatic biomarker and therapeutic target.

Keywords: C-SRC; CEACAM6; gastric cancer; invasion; metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / physiology*
  • Base Sequence
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / physiology*
  • Female
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / physiology
  • Gene Knockdown Techniques
  • Humans
  • Male
  • Mice
  • Middle Aged
  • Neoplasm Invasiveness / physiopathology*
  • Neoplasm Metastasis / physiopathology*
  • Phosphorylation
  • RNA, Small Interfering
  • Stomach Neoplasms / pathology*
  • Up-Regulation

Substances

  • Antigens, CD
  • CEACAM6 protein, human
  • Cell Adhesion Molecules
  • GPI-Linked Proteins
  • RNA, Small Interfering