P>Background There is continued interest in markers indicative of circulating melanoma cells. Nestin is a neuroepithelial intermediate filament protein that was found to be expressed in melanoma and in various cancer stem cells. Objectives We investigated expression of nestin in peripheral blood of patients with melanoma. Methods We analysed nestin expression by flow cytometry and by quantitative reverse transcription-polymerase chain reaction both in tissues (n = 23) and in blood samples (n = 102) from patients with American Joint Committee on Cancer stage III-IV melanoma. Forty-six negative controls were also added. Results Flow cytometry did not reveal nestin-expressing cells in peripheral blood of healthy volunteers. In patients with melanoma, however, nestin protein was expressed in a proportion of melanoma cells enriched from peripheral blood by immunomagnetic sorting. In melanoma tissue samples a significant correlation was found between mRNAs coding for nestin and tyrosinase (P = 0 center dot 001) and melan-A (P = 0 center dot 002), whereas in blood a significant correlation was observed only for tyrosinase (P = 0 center dot 015), but not for melan-A (P = 0 center dot 53). Nestin expression was higher in stage IV patients compared with stage III/IV with no evidence of disease, in patients with high tumour burden, and was positively correlated to expression of tyrosinase and melan-A. Conclusions Nestin was found to be an additional marker of interest for circulating melanoma cells. Prospective studies should investigate its potential added informative value in comparison with markers already in use for melanoma cell detection.
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Department of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Tajik P.
Barin A.
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Department of Clinical Pathology, Faculty of Veterinary Medicine, University of Tehran, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Barin A.
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Movahedin M.
Zarnani A.H.
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Nanobiotechnology Research Center, Avicenna Research Institute, ACECR, Tehran
Immunology Research Center, Iran University of Medical Sciences, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Zarnani A.H.
Hadavi R.
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Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Hadavi R.
Moghaddam G.
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Department of Animal Science, Faculty of Agriculture, University of Tabriz, TabrizDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Moghaddam G.
Shoja J.
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Department of Animal Science, Faculty of Agriculture, University of Tabriz, TabrizDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Shoja J.
Jeddi-Tehrani M.
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Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Jeddi-Tehrani M.
Ashrafi-Helan J.
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Department of Pathobiology, Faculty of Veterinary Medicine, University of Tabriz, TabrizDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Ashrafi-Helan J.
Heidari-Vala H.
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Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Heidari-Vala H.
Torkabadi E.
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Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran
Torkabadi E.
Qasemi-Panahi B.
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Department of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, TehranDepartment of Theriogenology, Faculty of Veterinary Medicine, University of Tehran, Tehran