Comparison of S100 protein and MIA protein as serum marker for malignant melanoma

Citation
D. Djukanovic et al., Comparison of S100 protein and MIA protein as serum marker for malignant melanoma, ANTICANC R, 20(3B), 2000, pp. 2203-2207
Citations number
26
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
3B
Year of publication
2000
Pages
2203 - 2207
Database
ISI
SICI code
0250-7005(200005/06)20:3B<2203:COSPAM>2.0.ZU;2-F
Abstract
Background Detection of S100 beta in serum has been shown to be a significa nt prognostic market for malignant melanoma in earlier studies. Melanoma in hibiting activity (MIA) has recently been detected as a new serum marker fo r malignant melanoma. Materials and Methods: In the present study, serum le vels of S100 beta protein and MIA were measured over a time period of up to 18 months in 271 serum samples from 65 melanoma patients at different stag es of disease, during chemotherapy and/or immunotherapy. In addition, 46 se ra of control patients were analysed The aim of this study was to compare b oth potential markers. S100 beta was measured using the immunoluminometric assay LIA-mat(A) Sangtec(R) (Byk Sangtec Diagnostica) with a cut-off level of 0.12 mu g/l. MLA was determined by the MIA ELISA kit (Roche) using a cut -off level of 6.5 ng/ml. Results: In 53 patients a direct correlation of S- 100 values and clinical course could be observed (81.5%), whereas in 48 pat ients MIA-values and clinical course (73.8%) showed an association. S100 be ta levels were incorrectly elevated in 5 out of 25 sera, "false positive" ( 20%) and were in 8 out of 40 sera not elevated despite the detection of met astases "false negative" (20%). Assessing the MLA levels, 2 out of 25 probe s were false positive (8%) and 13 out of 40 probes false negative(32.5%). C onclusion: Our data strongly suggest that S100 and MIA represent serum tumo r markers that are valuable both in therapy-monitoring and in defection of tumour progression.