Nm23-H1 suppresses tumor cell motility by down-regulating the lysophosphatidic acid receptor EDG2

Cancer Res. 2007 Aug 1;67(15):7238-46. doi: 10.1158/0008-5472.CAN-07-0962.

Abstract

Exogenous overexpression of the metastasis suppressor gene Nm23-H1 reduces the metastatic potential of multiple types of cancer cells and suppresses in vitro tumor cell motility and invasion. Mutational analysis of Nm23-H1 revealed that substitution mutants P96S and S120G did not inhibit motility and invasion. To elucidate the molecular mechanism of Nm23-H1 motility suppression, expression microarray analysis of an MDA-MB-435 cancer cell line overexpressing wild-type Nm23-H1 was done and cross-compared with expression profiles from lines expressing the P96S and S120G mutants. Nine genes, MET, PTN, SMO, FZD1, L1CAM, MMP2, NETO2, CTGF, and EDG2, were down-regulated by wild-type but not by mutant Nm23-H1 expression. Reduced expression of these genes coincident with elevated Nm23-H1 expression was observed in human breast tumor cohorts, a panel of breast carcinoma cell lines, and hepatocellular carcinomas from control versus Nm23-M1 knockout mice. The functional significance of the down-regulated genes was assessed by transfection and in vitro motility assays. Only EDG2 overexpression significantly restored motility to Nm23-H1-suppressed cancer cells, enhancing motility by 60-fold in these cells. In addition, silencing EDG2 expression with small interfering RNA reduced the motile phenotype of metastatic breast cancer cells. These data suggest that Nm23-H1 suppresses metastasis, at least in part, through down-regulation of EDG2 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • Cell Movement
  • Cohort Studies
  • Collagen / metabolism
  • Down-Regulation
  • Drug Combinations
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic / physiology*
  • Gene Silencing
  • Humans
  • Immunoblotting
  • Immunoenzyme Techniques
  • Laminin / metabolism
  • Mice
  • Mice, Knockout
  • NM23 Nucleoside Diphosphate Kinases
  • Nucleoside-Diphosphate Kinase / physiology*
  • Oligonucleotide Array Sequence Analysis
  • Proteoglycans / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Lysophosphatidic Acid / genetics
  • Receptors, Lysophosphatidic Acid / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Cells, Cultured

Substances

  • Drug Combinations
  • Laminin
  • NM23 Nucleoside Diphosphate Kinases
  • Proteoglycans
  • RNA, Messenger
  • Receptors, Lysophosphatidic Acid
  • matrigel
  • Collagen
  • NME1 protein, human
  • Nme1 protein, mouse
  • Nucleoside-Diphosphate Kinase