The value of tyrosinase messenger RNA (mRNA) detection by reverse-transcrip
tase polymerase chain reaction (RT-PCA) as a maker for circulating melanoma
cells remains controversial. However it has been suggested that detection
of melanoma cell mRNA may be used to evaluate prognosis and disease progres
sion in patients with advanced malignant melanoma. We used a highly sensiti
ve tyrosinase RT-PCR detection assay to test peripheral blood specimens of
80 patients with metastatic malignant melanoma. Moreover; we developed a mu
ltiple marker RT-PCR assay detecting a variety of additional melanocyte/tum
our specific markers addressing the potential heterogeneity of gene express
ion of circulating melanoma cells, Thus subgroups of 32 and 12 out of all t
he 80 patients weve also analysed for multimaker gene expression in their p
eripheral blood and bone marrow specimens, respectively. Altogether; 15 out
of 80 patients tested positive for one or move molecular markers with hete
rogeneous melanocyte/tumour gene expression patterns. All RT- PCR positive
patients presented with progressive and widely disseminated disease. We con
cluded that the detection of melanoma cell mRNA occurs in a stage of massiv
e tumour progression and may predict poor clinical outcome in advanced mali
gnant melanoma patients (p<0.001). In addition, the multiple maker RT-PCR a
nalysis was more reliable and sensitive than a single molecular marker assa
y for the detection of melanoma cells.