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Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications

Stem cell factor (SCF), the ligand for c-Kit, is known to regulate developmental and functional processes of haematopoietic stem cells, mast cells and melanocytes. Two different splice variants form predominantly soluble (sSCF or SCF-1) and in addition some membrane-bound SCF (mSCF or SCF-2). In ord...

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Autores principales: Welker, P, Schadendorf, D, Artuc, M, Grabbe, J, Henz, B M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363371/
https://www.ncbi.nlm.nih.gov/pubmed/10780526
http://dx.doi.org/10.1054/bjoc.1999.1076
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author Welker, P
Schadendorf, D
Artuc, M
Grabbe, J
Henz, B M
author_facet Welker, P
Schadendorf, D
Artuc, M
Grabbe, J
Henz, B M
author_sort Welker, P
collection PubMed
description Stem cell factor (SCF), the ligand for c-Kit, is known to regulate developmental and functional processes of haematopoietic stem cells, mast cells and melanocytes. Two different splice variants form predominantly soluble (sSCF or SCF-1) and in addition some membrane-bound SCF (mSCF or SCF-2). In order to explore the prognostic significance of these molecules in melanoma, total SCF, SCF splice variants and c-Kit expression were studied in normal skin melanocytes and in 11 different melanoma cell lines, using reverse transcription polymerase chain reaction, immunocytochemistry and enzyme-linked immunosorbent assay. Nine of the 11 melanoma cell lines expressed SCF-1 mRNA, only two of them SCF-2, and these two also SCF-1. Coexpression of both SCF-1 and c-Kit was noted in five cell lines, and only one cell line as well as normal melanocytes expressed both SCF-1 and SCF-2 as well as c-Kit. Corresponding results were obtained on immunocytochemical staining. Of three exemplary melanoma cell lines studied, two expressing SCF mRNA also released SCF spontaneously and on stimulation, whereas the line lacking SCF and c-kit mRNA (SK-Mel-23) failed to do so. These data demonstrate thus that melanoma cell lines, particularly those known to metastasize in vivo, lose the ability to express SCF-2 mRNA, suggesting that this molecule may serve, next to c-Kit, as a prognostic marker for malignant melanoma. © 2000 Cancer Research Campaign
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spelling pubmed-23633712009-09-10 Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications Welker, P Schadendorf, D Artuc, M Grabbe, J Henz, B M Br J Cancer Regular Article Stem cell factor (SCF), the ligand for c-Kit, is known to regulate developmental and functional processes of haematopoietic stem cells, mast cells and melanocytes. Two different splice variants form predominantly soluble (sSCF or SCF-1) and in addition some membrane-bound SCF (mSCF or SCF-2). In order to explore the prognostic significance of these molecules in melanoma, total SCF, SCF splice variants and c-Kit expression were studied in normal skin melanocytes and in 11 different melanoma cell lines, using reverse transcription polymerase chain reaction, immunocytochemistry and enzyme-linked immunosorbent assay. Nine of the 11 melanoma cell lines expressed SCF-1 mRNA, only two of them SCF-2, and these two also SCF-1. Coexpression of both SCF-1 and c-Kit was noted in five cell lines, and only one cell line as well as normal melanocytes expressed both SCF-1 and SCF-2 as well as c-Kit. Corresponding results were obtained on immunocytochemical staining. Of three exemplary melanoma cell lines studied, two expressing SCF mRNA also released SCF spontaneously and on stimulation, whereas the line lacking SCF and c-kit mRNA (SK-Mel-23) failed to do so. These data demonstrate thus that melanoma cell lines, particularly those known to metastasize in vivo, lose the ability to express SCF-2 mRNA, suggesting that this molecule may serve, next to c-Kit, as a prognostic marker for malignant melanoma. © 2000 Cancer Research Campaign Nature Publishing Group 2000-04 2000-03-21 /pmc/articles/PMC2363371/ /pubmed/10780526 http://dx.doi.org/10.1054/bjoc.1999.1076 Text en Copyright © 2000 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Welker, P
Schadendorf, D
Artuc, M
Grabbe, J
Henz, B M
Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
title Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
title_full Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
title_fullStr Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
title_full_unstemmed Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
title_short Expression of SCF splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
title_sort expression of scf splice variants in human melanocytes and melanoma cell lines: potential prognostic implications
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363371/
https://www.ncbi.nlm.nih.gov/pubmed/10780526
http://dx.doi.org/10.1054/bjoc.1999.1076
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