Lymphoma cells express patterns of adhesion molecules that impart inte
raction potential with other cells and extracellular matrix components
. The expression of these molecules can be controlled in a tissue-spec
ific fashion by developmentally programmed or inducible genetic regula
tory mechanisms, while at the single-cell level, adhesion receptor fun
ction can be regulated by induction of intracellular biochemical chang
es that influence receptor avidity. Ligation of adhesion molecules can
lead to secondary signaling events and the positive or negative regul
ation of gene expression. Thus adhesion not only provides points for s
tatic contact, but can change the phenotype of the adhering cell. Sinc
e the adhesive personality of lymphoma cells can be predicted by pheno
typic determinations, a systematic evaluation of lymphoma surface adhe
sion receptors may provide valuable clues to dissecting the origins of
this disease, and promises to provide valuable prognostic indices for
predicting lymphoma metastatic patterns.