Effect of N-CAM on in vitro invasion of human adenoid cystic carcinoma cells

Oral Oncol. 2001 Dec;37(8):638-42. doi: 10.1016/s1368-8375(01)00007-0.

Abstract

Adenoid cystic carcinoma of salivary glands is characterised by aggressive behaviour, high rate of local recurrences, neurotropism and late metastasis. In a previous work we demonstrated that adenoid cystic carcinoma cultured cells (CAC2 cells) expressed N-CAM. It was suggested that this expression, modulated by extracellular matrix, would be correlated to cell movement. The aim of our study was to verify whether CAC2 cells presented invasion capacity. Moreover, we tested whether the neural adhesion molecule (N-CAM) would participate in this process. CAC2 cells were either previously treated, or not (control), with a monoclonal antibody against N-CAM. Invasion assays were carried out using a modified Boyden chamber (Transwell chamber). CAC2 cells (10(5)) were dispensed into Transwell upper chamber on the top of Matrigel coated filter. The cells that invaded the filters in the first 8 h were counted under light microscopy, yielding data for the invasion rates (%). Control CAC2 cells presented an invasion rate of 5.28+/-0.04%. The invasion rate raised to 6.53+/-0.2% when N-CAM was blocked with monoclonal antibody. N-CAM impaired the adenoid cystic carcinoma cell invasion in vitro. Therefore, we suggest an anti-invasive role for N-CAM in adenoid cystic carcinoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Antibodies, Monoclonal / immunology
  • Carcinoma, Adenoid Cystic / pathology*
  • Cell Count
  • Fluorescent Antibody Technique
  • Humans
  • Microscopy, Fluorescence
  • Neoplasm Invasiveness
  • Neural Cell Adhesion Molecules / physiology*
  • Parotid Neoplasms / pathology*
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Neural Cell Adhesion Molecules