Overexpression of KAI1 suppresses in vitro invasiveness and in vivo metastasis in breast cancer cells

Cancer Res. 2001 Jul 1;61(13):5284-8.

Abstract

KAI1 is a metastasis suppressor gene for human prostate cancer and is also involved in the progression of a variety of other human cancers. Previously, we have demonstrated that KAI1 expression was down-regulated in metastatic breast cancer cell lines as well as in highly aggressive breast cancer specimens. To determine whether KAI1 expression is responsible for the metastasis suppression in breast cancer, we transfected the human KAI1 cDNA into two highly malignant breast cancer cell lines, LCC6 and MDA-MB-231, which both have low levels of endogenous KAI1 expression. Parental, vector-only transfectants and KAI1 transfectant clones were injected into the mammary fat pads and tail veins, respectively, of athymic nude mice and assessed for both spontaneous and experimental lung metastasis. High KAI1 expression significantly suppressed the metastatic potential of KAI1-transfected LCC6 cells. Metastasis suppression correlated with the reduced rate of tumor growth and a decreased clonogenicity in soft agar. Furthermore, KAI1 expression significantly suppressed the in vitro cell invasion in KAI1-transfected MDA-MB-231 cells. Our results suggested that KAI1 may function as a negative regulator of breast cancer metastasis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD / biosynthesis
  • Antigens, CD / genetics
  • Antigens, CD / physiology*
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / immunology
  • Breast Neoplasms / pathology*
  • Cell Adhesion / physiology
  • Cell Division / physiology
  • DNA, Complementary / genetics
  • Female
  • Genes, Tumor Suppressor
  • Humans
  • Kangai-1 Protein
  • Lung Neoplasms / secondary
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / physiology*
  • Mice
  • Mice, Nude
  • Proto-Oncogene Proteins*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Antigens, CD
  • CD82 protein, human
  • Cd82 antigen, mouse
  • DNA, Complementary
  • Kangai-1 Protein
  • Membrane Glycoproteins
  • Proto-Oncogene Proteins