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PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes
Melanoma is one of the most aggressive types of cancer wherein resistance to treatment prevails. Therefore, it is important to discover novel molecular targets of melanoma progression as potential treatments. Here we show that paired-like homeodomain transcription factor 1 (PITX1) plays a crucial ro...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443576/ https://www.ncbi.nlm.nih.gov/pubmed/34526609 http://dx.doi.org/10.1038/s41598-021-97791-6 |
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author | Ohira, Takahito Nakagawa, Suguru Takeshita, Jumpei Aburatani, Hiroyuki Kugoh, Hiroyuki |
author_facet | Ohira, Takahito Nakagawa, Suguru Takeshita, Jumpei Aburatani, Hiroyuki Kugoh, Hiroyuki |
author_sort | Ohira, Takahito |
collection | PubMed |
description | Melanoma is one of the most aggressive types of cancer wherein resistance to treatment prevails. Therefore, it is important to discover novel molecular targets of melanoma progression as potential treatments. Here we show that paired-like homeodomain transcription factor 1 (PITX1) plays a crucial role in the inhibition of melanoma progression through regulation of SRY-box transcription factors (SOX) gene family mRNA transcription. Overexpression of PITX1 in melanoma cell lines resulted in a reduction in cell proliferation and an increase in apoptosis. Additionally, analysis of protein levels revealed an antagonistic cross-regulation between SOX9 and SOX10. Interestingly, PITX1 binds to the SOX9 promoter region as a positive regulatory transcription factor; PITX1 mRNA expression levels were positively correlated with SOX9 expression, and negatively correlated with SOX10 expression in melanoma tissues. Furthermore, transcription of the long noncoding RNA (lncRNA), survival-associated mitochondrial melanoma-specific oncogenic noncoding RNA (SAMMSON), was decreased in PITX1-overexpressing cells. Taken together, the findings in this study indicate that PITX1 may act as a negative regulatory factor in the development and progression of melanoma via direct targeting of the SOX signaling. |
format | Online Article Text |
id | pubmed-8443576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84435762021-09-20 PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes Ohira, Takahito Nakagawa, Suguru Takeshita, Jumpei Aburatani, Hiroyuki Kugoh, Hiroyuki Sci Rep Article Melanoma is one of the most aggressive types of cancer wherein resistance to treatment prevails. Therefore, it is important to discover novel molecular targets of melanoma progression as potential treatments. Here we show that paired-like homeodomain transcription factor 1 (PITX1) plays a crucial role in the inhibition of melanoma progression through regulation of SRY-box transcription factors (SOX) gene family mRNA transcription. Overexpression of PITX1 in melanoma cell lines resulted in a reduction in cell proliferation and an increase in apoptosis. Additionally, analysis of protein levels revealed an antagonistic cross-regulation between SOX9 and SOX10. Interestingly, PITX1 binds to the SOX9 promoter region as a positive regulatory transcription factor; PITX1 mRNA expression levels were positively correlated with SOX9 expression, and negatively correlated with SOX10 expression in melanoma tissues. Furthermore, transcription of the long noncoding RNA (lncRNA), survival-associated mitochondrial melanoma-specific oncogenic noncoding RNA (SAMMSON), was decreased in PITX1-overexpressing cells. Taken together, the findings in this study indicate that PITX1 may act as a negative regulatory factor in the development and progression of melanoma via direct targeting of the SOX signaling. Nature Publishing Group UK 2021-09-15 /pmc/articles/PMC8443576/ /pubmed/34526609 http://dx.doi.org/10.1038/s41598-021-97791-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ohira, Takahito Nakagawa, Suguru Takeshita, Jumpei Aburatani, Hiroyuki Kugoh, Hiroyuki PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes |
title | PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes |
title_full | PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes |
title_fullStr | PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes |
title_full_unstemmed | PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes |
title_short | PITX1 inhibits the growth and proliferation of melanoma cells through regulation of SOX family genes |
title_sort | pitx1 inhibits the growth and proliferation of melanoma cells through regulation of sox family genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8443576/ https://www.ncbi.nlm.nih.gov/pubmed/34526609 http://dx.doi.org/10.1038/s41598-021-97791-6 |
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