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The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma

Clear cell sarcoma (CCS) is associated with the EWS/ATF1 oncogene that is created by chromosomal fusion of the Ewings Sarcoma oncogene (EWS) and the cellular transcription factor ATF1. The melanocytic character of CCS suggests that the microphthalmia-associated transcription factor (Mitf), a major i...

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Autores principales: Li, K K C, Goodall, J, Goding, C R, Liao, S-K, Wang, C-H, Lin, Y-C, Hiraga, H, Nojima, T, Nagashima, K, Schaefer, K-L, Lee, K A W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376962/
https://www.ncbi.nlm.nih.gov/pubmed/12966428
http://dx.doi.org/10.1038/sj.bjc.6601212
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author Li, K K C
Goodall, J
Goding, C R
Liao, S-K
Wang, C-H
Lin, Y-C
Hiraga, H
Nojima, T
Nagashima, K
Schaefer, K-L
Lee, K A W
author_facet Li, K K C
Goodall, J
Goding, C R
Liao, S-K
Wang, C-H
Lin, Y-C
Hiraga, H
Nojima, T
Nagashima, K
Schaefer, K-L
Lee, K A W
author_sort Li, K K C
collection PubMed
description Clear cell sarcoma (CCS) is associated with the EWS/ATF1 oncogene that is created by chromosomal fusion of the Ewings Sarcoma oncogene (EWS) and the cellular transcription factor ATF1. The melanocytic character of CCS suggests that the microphthalmia-associated transcription factor (Mitf), a major inducer of melanocytic differentiation, may be miss-expressed in CCS. Accordingly, we show that the mRNA and protein of the melanocyte-specific isoform of Mitf (Mitf-M) are present in several cultured CCS cell lines (Su-ccs-1, DTC1, Kao, MST-1, MST-2 and MST-3). The above cell lines thus provide a valuable experimental resource for examining the role of Mitf-M in both CCS and melanocyte differentiation. Melanocyte-specific expression of Mitf-M is achieved via an ATF-dependent melanocyte-specific cAMP-response element in the Mitf-M promoter, and expression of Mitf-M in CCS cells suggests that EWS/ATF1 (a potent and promiscuous activator of cAMP-inducible promoters) may activate the Mitf-M promoter. Surprisingly, however, the Mitf-M promoter is not activated by EWS/ATF1 in transient assays employing CCS cells, melanocytes or nonmelanocytic cells. Thus, our results indicate that Mitf-M promoter activation may require an appropriate chromosomal context in CCS cells or alternatively that the Mitf-M promoter is not directly activated by EWS/ATF1.
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spelling pubmed-23769622009-09-10 The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma Li, K K C Goodall, J Goding, C R Liao, S-K Wang, C-H Lin, Y-C Hiraga, H Nojima, T Nagashima, K Schaefer, K-L Lee, K A W Br J Cancer Molecular and Cellular Pathology Clear cell sarcoma (CCS) is associated with the EWS/ATF1 oncogene that is created by chromosomal fusion of the Ewings Sarcoma oncogene (EWS) and the cellular transcription factor ATF1. The melanocytic character of CCS suggests that the microphthalmia-associated transcription factor (Mitf), a major inducer of melanocytic differentiation, may be miss-expressed in CCS. Accordingly, we show that the mRNA and protein of the melanocyte-specific isoform of Mitf (Mitf-M) are present in several cultured CCS cell lines (Su-ccs-1, DTC1, Kao, MST-1, MST-2 and MST-3). The above cell lines thus provide a valuable experimental resource for examining the role of Mitf-M in both CCS and melanocyte differentiation. Melanocyte-specific expression of Mitf-M is achieved via an ATF-dependent melanocyte-specific cAMP-response element in the Mitf-M promoter, and expression of Mitf-M in CCS cells suggests that EWS/ATF1 (a potent and promiscuous activator of cAMP-inducible promoters) may activate the Mitf-M promoter. Surprisingly, however, the Mitf-M promoter is not activated by EWS/ATF1 in transient assays employing CCS cells, melanocytes or nonmelanocytic cells. Thus, our results indicate that Mitf-M promoter activation may require an appropriate chromosomal context in CCS cells or alternatively that the Mitf-M promoter is not directly activated by EWS/ATF1. Nature Publishing Group 2003-09-15 2003-09-09 /pmc/articles/PMC2376962/ /pubmed/12966428 http://dx.doi.org/10.1038/sj.bjc.6601212 Text en Copyright © 2003 Cancer Research UK 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 Molecular and Cellular Pathology
Li, K K C
Goodall, J
Goding, C R
Liao, S-K
Wang, C-H
Lin, Y-C
Hiraga, H
Nojima, T
Nagashima, K
Schaefer, K-L
Lee, K A W
The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma
title The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma
title_full The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma
title_fullStr The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma
title_full_unstemmed The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma
title_short The melanocyte inducing factor MITF is stably expressed in cell lines from human clear cell sarcoma
title_sort melanocyte inducing factor mitf is stably expressed in cell lines from human clear cell sarcoma
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376962/
https://www.ncbi.nlm.nih.gov/pubmed/12966428
http://dx.doi.org/10.1038/sj.bjc.6601212
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