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A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression
BACKGROUND: Translocated in liposarcoma-CCAAT/enhancer binding protein homologous protein (TLS–CHOP) (also known as FUS-DDIT3) chimeric oncoprotein is found in the majority of human myxoid liposarcoma (MLS), but its molecular function remains unclear. METHODS: We knockdowned TLS–CHOP expression in M...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388565/ https://www.ncbi.nlm.nih.gov/pubmed/22588557 http://dx.doi.org/10.1038/bjc.2012.199 |
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author | Oikawa, K Tanaka, M Itoh, S Takanashi, M Ozaki, T Muragaki, Y Kuroda, M |
author_facet | Oikawa, K Tanaka, M Itoh, S Takanashi, M Ozaki, T Muragaki, Y Kuroda, M |
author_sort | Oikawa, K |
collection | PubMed |
description | BACKGROUND: Translocated in liposarcoma-CCAAT/enhancer binding protein homologous protein (TLS–CHOP) (also known as FUS-DDIT3) chimeric oncoprotein is found in the majority of human myxoid liposarcoma (MLS), but its molecular function remains unclear. METHODS: We knockdowned TLS–CHOP expression in MLS-derived cell lines by a specific small interfering RNA, and analysed the gene expression profiles with microarray. RESULTS: TLS-CHOP knockdown inhibited growth of MLS cells, and induced an anticancer cytokine, melanoma differentiation-associated gene 7 (MDA-7)/interleukin-24 (IL-24) expression. However, double knockdown of TLS–CHOP and MDA-7/IL-24 did not inhibit MLS cell growth. CONCLUSION: Repression of MDA-7/IL-24 expression by TLS–CHOP is required for MLS tumour growth, and TLS–CHOP may become a promising therapeutic target for MLS treatment. |
format | Online Article Text |
id | pubmed-3388565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-33885652013-06-05 A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression Oikawa, K Tanaka, M Itoh, S Takanashi, M Ozaki, T Muragaki, Y Kuroda, M Br J Cancer Short Communication BACKGROUND: Translocated in liposarcoma-CCAAT/enhancer binding protein homologous protein (TLS–CHOP) (also known as FUS-DDIT3) chimeric oncoprotein is found in the majority of human myxoid liposarcoma (MLS), but its molecular function remains unclear. METHODS: We knockdowned TLS–CHOP expression in MLS-derived cell lines by a specific small interfering RNA, and analysed the gene expression profiles with microarray. RESULTS: TLS-CHOP knockdown inhibited growth of MLS cells, and induced an anticancer cytokine, melanoma differentiation-associated gene 7 (MDA-7)/interleukin-24 (IL-24) expression. However, double knockdown of TLS–CHOP and MDA-7/IL-24 did not inhibit MLS cell growth. CONCLUSION: Repression of MDA-7/IL-24 expression by TLS–CHOP is required for MLS tumour growth, and TLS–CHOP may become a promising therapeutic target for MLS treatment. Nature Publishing Group 2012-06-05 2012-05-15 /pmc/articles/PMC3388565/ /pubmed/22588557 http://dx.doi.org/10.1038/bjc.2012.199 Text en Copyright © 2012 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 | Short Communication Oikawa, K Tanaka, M Itoh, S Takanashi, M Ozaki, T Muragaki, Y Kuroda, M A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression |
title | A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression |
title_full | A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression |
title_fullStr | A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression |
title_full_unstemmed | A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression |
title_short | A novel oncogenic pathway by TLS–CHOP involving repression of MDA-7/IL-24 expression |
title_sort | novel oncogenic pathway by tls–chop involving repression of mda-7/il-24 expression |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388565/ https://www.ncbi.nlm.nih.gov/pubmed/22588557 http://dx.doi.org/10.1038/bjc.2012.199 |
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