Cell adhesion molecules are glycoproteins expressed on the cell surfac
e and play an important role in inflammatory as well as neoplastic dis
eases. There are four main groups: the integrin family, the immunoglob
ulin superfamily, selectins, and cadherins. The integrin family has ei
ght subfamilies, designated as beta(1), through beta(8). The most wide
ly studied subfamilies are beta(1) (CD29, very late activation [VLA] m
embers), beta(2) (leukocyte integrins such as CDlla/CD18, CD11b/CD18,
CD11c/CD18, and alpha(d),beta(2)), beta(3) (CD61, cytoadhesions), and
beta(7) (alpha(4) beta(7) and alpha(E) beta(7)). The immunoglobulin su
perfamily includes leukocyte function antigen-2 (LFA-2 or CD2), leukoc
yte function antigen-3 (LFA-3 or CD58), intercellular adhesion molecul
es (ICAMs), vascular adhesion molecule-1 (VCAM-1), platelet-endothelia
l cell adhesion molecule-1 (PE-CAM-1), and mucosal addressin cell adhe
sion molecule-1 (MAdCAM-1). The selectin family includes E-selectin (C
D62E), P-selectin (CD62P), and L-selectin (CD62L). Cadherins are major
cell-cell adhesion molecules and include epithelial (E), placental (P
), and neural (N) subclasses. The binding sites (ligands/receptors) ar
e different for each of these cell adhesion molecules (e.g., ICAM bind
s to CD11/CD18; VCAM-1 binds to VLA-4). The specific cell adhesion mol
ecules and their ligands that may be involved in pathologic conditions
and potential therapeutic strategies by modulating the expression of
these molecules will be discussed.