The NM23 gene has been proposed as a metastasis-suppressor gene, and i
ts use has been suggested as prognostic factor. NM23 was identified in
a system of murine melanoma cell lines, in which an inverse relations
hip was found between NM23 expression and metastatic ability. In a hum
an malignant melanoma study NM23 expression was found to be significan
tly lower in metastases that developed less than 24 months after diagn
osis of the primary tumours. The present paper studies the expression
of the NM23.H1 gene in cell lines which derive from primary or metasta
tic human malignant melanomas in relation to staging, infiltration deg
ree, lymphocytic infiltration, cell morphology, cell pigmentation, kar
yotype, and disease-free survival. The level of mRNA expression of the
NM23 gene is significantly lower in cell lines that derive from more
infiltrating primary melanomas than in cell lines obtained from less i
nfiltrating tumours. Moreover, cell lines derived from tumours of pati
ents with a disease-free survival of more than 24 months (24-58 months
) express the NM23 gene at higher levels than cell lines obtained from
melanomas of patients with a disease-free survival of less than 24 mo
nths (6-15 months).