S100B PROTEIN, 5-S-CYSTEINYLDOPA AND 6-HYDROXY-5-METHOXYINDOLE-2-CARBOXYLIC ACID AS BIOCHEMICAL MARKERS FOR SURVIVAL PROGNOSIS IN PATIENTS WITH MALIGNANT-MELANOMA
R. Karnell et al., S100B PROTEIN, 5-S-CYSTEINYLDOPA AND 6-HYDROXY-5-METHOXYINDOLE-2-CARBOXYLIC ACID AS BIOCHEMICAL MARKERS FOR SURVIVAL PROGNOSIS IN PATIENTS WITH MALIGNANT-MELANOMA, Melanoma research, 7(5), 1997, pp. 393-399
Citations number
39
Categorie Soggetti
Medicine, Research & Experimental",Oncology,"Dermatology & Venereal Diseases
Elevated levels of the phaeomelanin metabolite 5-S-cysteinyldopa and t
he eumelanin metabolite 6-hydroxy-5-methoxyindole-2-carboxylic acid in
urine and serum have been shown in previous studies to correlate with
disseminated malignant melanoma. Immunohistochemical detection of S10
0B protein is an acknowledged method for the diagnosis of malignant me
lanoma, and it has been suggested that rising serum levels of S100B pr
otein are associated with the survival rate of patients with malignant
melanoma. In the present study serum levels of S100B protein and urin
ary concentrations of 5-S-cysteinyldopa and 6-hydroxy-5-methoxyindole-
2-carboxylic acid were measured in 91 patients with histopathologicall
y verified malignant melanoma. At the time of sampling 13 patients wer
e in clinical stage I, 13 in stage II and 65 in stage III. The urinary
levels of the melanin metabolites were determined by automated high p
erformance liquid chromatography, and the serum levels of S100B protei
n by an immunoradiometric assay with two monoclonal antibodies. The ov
erall survival rate was most strongly associated with the serum levels
of S100B protein (P < 0.001), but there was also a significant correl
ation to urinary levels of 5-S-cysteinyldopa (P < 0.001). A correspond
ing association with urinary levels of 6-hydroxy-5-methoxyindole-2-car
boxylic acid was found in only a very few patients with extremely high
urinary concentrations. A statistically significant increase in relat
ive hazard was found for S100B protein levels exceeding 0.6 mu g/l (P
< 0.001), and predictably for patients in clinical stage III (P < 0.00
1). An analysis of S100B protein levels in patients in clinical stage
III showed a significant correlation to survival (P = 0.005). Our stud
y suggests that of the three biochemical tumour markers, S100B and to
a lesser extent 5-S-cysteinyldopa have the greatest potential to be us
ed as predictors of survival prognosis in patients with malignant mela
noma.