Background and Objectives: Anatomic extent is not the sole axis of classifi
cation of tumors and of tumor patients relevant to treatment planning and e
stimation of prognosis. This results in the need to demonstrate an improvem
ent in prognostic assessment and choice of therapy achieved by consideratio
n of factors other than TNM. nm23 protein does prevent tumor from metastasi
zing and may also play a role in the control of growth and development. The
purpose of this study was to elucidate the clinical significance of nm23 e
xpression in human anal canal carcinoma and to evaluate its influence on th
e outcome of patients after surgery or radiochemotherapy.
Methods: Twenty-two patients affected by anal canal carcinoma were evaluate
d. Each section was incubated with monoclonal antibody nm23 NDPK-A. Immunos
taining was considered positive when at least 10% of the tumor cells were i
mmunostained.
Results: nm23 immunoreactivity was detected in 6/22 (27.3%) tumors. No sign
ificant association was found between nm23 expression and prognosis.
Conclusions: The mechanisms causing enhanced nm23-H1 expression in anal can
al carcinoma are unknown. Although the level and expression were not correl
ated with prognosis, activation of nm23-H1 gene might be a prerequisite for
oncogenesis in this type of tumor, while an alternate possibility is the m
odification of cellular characteristics in relation to proliferation and/or
differentiation as a consequence of oncogenesis. J. Surg. Oncol. 2000;74:1
63-166. (C) 2000 Wiley-Liss, Inc.