The presence of the neural cell adhesion molecule, NCAM, is indicative
for a poor prognosis in lung-cancer patients. Using MAb 735, we have
investigated the expression of polysialic acid, PSA, on NCAM in a spec
trum of neuro-endocrine lung tumors, ranging from the slowly growing t
ypical carcinoids via the atypical carcinoids with clinically unpredic
table behavior to the highly aggressive small-cell lung carcinomas. Ou
r immunohistochemical findings indicate a significant association betw
een the presence of PSA on the tumor cells and an aggressive and immat
ure sub-type of the tumor. This might be related to impairment of cell
-cell and cell-matrix interactions by the presence of PSA, as we demon
strated in vitro, since detachment is one of the first steps in the me
tastatic process. The NCAM-MAb 123C3 used in these studies appeared ex
tremely useful in immunoscintigraphy and immunotherapy of SCLC xenogra
fts in nude mice, and for immunoscintigraphy of a SCLC patient. This m
ay be explained by internalization of the 123C3 antibody, which we dem
onstrated in vitro. 123C3 is the only Cluster-1 SCLC Mab studied thus
fat that becomes internalized. (C) 1994 Wiley-Liss, Inc.