Protein-bound polysaccharide PSK inhibits tumor invasiveness by down-regulation of TGF-beta1 and MMPs

Clin Exp Metastasis. 2000;18(4):343-52. doi: 10.1023/a:1010897432244.

Abstract

Transforming growth factor beta1 (TGF-beta1) and matrix metalloproteinases (MMPs) produced by tumor cells play important roles in tumor invasion. PSK, a protein-bound polysaccharide, is widely used in Japan as an immunopotentiating biological response modifier for cancer patients. In this study, we focused on the effects of PSK on invasiveness, TGF-beta1 production, and MMPs expression in two human tumor cell lines, pancreatic cancer cell line (NOR-P1) and gastric cancer cell line (MK-1P3). PSK significantly decreased the invasiveness of both cell lines through Matrigel-coated filters but did not affect cell viability, proliferation, or adhesion. Decreased invasion was associated with the inhibition of TGF-beta1, MMP-2, and MMP-9 at both mRNA and protein levels as assessed by reverse transcriptase-polymerase chain reaction, gelatin zymography, and enzyme-linked immunosorbent assay. Antibody against TGF-beta1 neutralized the MMP activities of both cell lines. PSK also suppressed the expression of urokinase plasminogen activator (uPA) and uPA receptor but did not change plasminogen activator inhibitor-1 (PAI-1) expression. Western blot analysis showed that PSK reduced uPA protein expression but not PAI-1 expression in the both cell lines. These results indicate that PSK suppresses tumor cell invasiveness through down-regulation of several invasion-related factors including TGF-beta1, uPA, MMP-2, and MMP-9.

MeSH terms

  • Adjuvants, Immunologic / pharmacology*
  • Antibiotics, Antineoplastic / pharmacology*
  • Cell Adhesion / drug effects
  • Cell Division / drug effects
  • Collagen
  • Down-Regulation
  • Drug Combinations
  • Drug Screening Assays, Antitumor
  • Humans
  • Laminin
  • Matrix Metalloproteinases / drug effects*
  • Matrix Metalloproteinases / metabolism
  • Neoplasm Invasiveness
  • Neoplasm Proteins / drug effects*
  • Neoplasm Proteins / metabolism
  • Pancreatic Neoplasms / pathology
  • Proteoglycans / pharmacology*
  • Stomach Neoplasms / pathology
  • Transforming Growth Factor beta / drug effects*
  • Transforming Growth Factor beta / metabolism
  • Transforming Growth Factor beta1
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / pathology

Substances

  • Adjuvants, Immunologic
  • Antibiotics, Antineoplastic
  • Drug Combinations
  • Laminin
  • Neoplasm Proteins
  • Proteoglycans
  • TGFB1 protein, human
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • matrigel
  • polysaccharide-K
  • Collagen
  • Matrix Metalloproteinases