A chimeric antibody targeting CD147 inhibits hepatocellular carcinoma cell motility via FAK-PI3K-Akt-Girdin signaling pathway

Clin Exp Metastasis. 2015 Jan;32(1):39-53. doi: 10.1007/s10585-014-9689-7. Epub 2014 Nov 26.

Abstract

CD147 is expressed at low levels in normal tissues but frequently highly expressed in a wide range of tumor types such as lung, breast, and liver and therefore it is a potentially unique therapeutic target for these diverse tumor types. We previously generated a murine antibody HAb18 which suppresses matrix met al.loproteinase-2 and matrix metalloproteinase-9 secretion, attenuates cell invasion by blocking the CD147 molecule in tumor cells. Here, we generated a chimeric antibody containing the variable heavy and variable light chains of murine HAb18 and the constant regions of human IgG1γ1 and human κ chain as a potential therapeutic agent (designated cHAb18). Quantitative measurement of cHAb18 antibody affinity for antigen CD147 with surface plasmon resonance showed the equilibrium dissociation constant KD was 2.66 × 10(-10) mol/L, similar to that of KD 2.73 × 10(-10) mol/L for murine HAb18. cHAb18 induced antibody-dependent cell-mediated cytotoxicity in two hepatocellular carcinoma cell lines, SMMC-7721 and Huh-7 cells. It inhibited cancer invasion and migration in hepatocellular carcinoma cells by specifically blocking CD147. Except for the depression of matrix metalloproteinase-2 and matrix metalloproteinase-9 expressions, cHAb18 antibody suppressed cell motility by rearrangement of actin cytoskeleton, which was probably induced by decreasing the phosphorylation of focal adhesion kinase, phosphatidylinositide-3 kinase (PI3K), Akt, and Girdin in the integrin signaling pathway. In an orthotopic model of hepatocellular carcinoma in BALB/c nude mice, cHAb18 treatment effectively reduced the tumor metastasis in liver and prolonged the survival. These findings reveal new therapeutic potential for cHAb18 antibody targeting CD147 on tumor therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies / genetics
  • Antibodies / therapeutic use*
  • Antibody-Dependent Cell Cytotoxicity / immunology
  • Basigin / immunology*
  • CHO Cells
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / secondary
  • Cell Line, Tumor
  • Cell Movement / drug effects*
  • Cricetulus
  • Female
  • Focal Adhesion Kinase 1 / metabolism
  • Hep G2 Cells
  • Humans
  • Hydroxamic Acids / pharmacology
  • Immunoglobulin G / immunology
  • Immunoglobulin kappa-Chains / immunology
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / pathology
  • Matrix Metalloproteinase 2 / immunology
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / immunology
  • Matrix Metalloproteinase 9 / metabolism
  • Matrix Metalloproteinase Inhibitors / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Microfilament Proteins / metabolism
  • Neoplasm Invasiveness
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-akt / metabolism
  • Pseudopodia / immunology
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / therapeutic use*
  • Signal Transduction
  • Single-Chain Antibodies / immunology
  • Stress Fibers / immunology
  • Vesicular Transport Proteins / metabolism

Substances

  • Antibodies
  • Bsg protein, mouse
  • Hydroxamic Acids
  • Immunoglobulin G
  • Immunoglobulin kappa-Chains
  • Matrix Metalloproteinase Inhibitors
  • Microfilament Proteins
  • Recombinant Fusion Proteins
  • Single-Chain Antibodies
  • Vesicular Transport Proteins
  • girdin protein, mouse
  • Basigin
  • marimastat
  • Phosphatidylinositol 3-Kinases
  • Focal Adhesion Kinase 1
  • Ptk2 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • Matrix Metalloproteinase 2
  • Mmp2 protein, mouse
  • Matrix Metalloproteinase 9
  • Mmp9 protein, mouse