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LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression
Recently studies found that APEX1 was abnormally expressed in melanoma, indicating that it might be involved in the development of melanoma. However, the underlying mechanism and the interaction between APEX1 and LINC00470 in melanoma are not clear. Therefore, we aimed to investigate the role of LIN...
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/PMC8055894/ https://www.ncbi.nlm.nih.gov/pubmed/33875645 http://dx.doi.org/10.1038/s41419-021-03612-z |
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author | Huang, Ting Wang, Yong-Jie Huang, Mi-Tao Guo, Yu Yang, Li-Chang Liu, Xiao-Jin Tan, Wu-Yuan Long, Jian-Hong |
author_facet | Huang, Ting Wang, Yong-Jie Huang, Mi-Tao Guo, Yu Yang, Li-Chang Liu, Xiao-Jin Tan, Wu-Yuan Long, Jian-Hong |
author_sort | Huang, Ting |
collection | PubMed |
description | Recently studies found that APEX1 was abnormally expressed in melanoma, indicating that it might be involved in the development of melanoma. However, the underlying mechanism and the interaction between APEX1 and LINC00470 in melanoma are not clear. Therefore, we aimed to investigate the role of LINC00470 in the development of melanoma in this work. We discovered that LINC00470 was overexpressed in melanoma tissues and cells compared with the adjacent normal tissues and cells by qPCR. The overexpression of LINC00470 promoted the proliferation and migration of melanoma cells. The functional investigation demonstrated that LINC00470 activated the transcription factor, ZNF131, to regulate the APEX1 expression, which finally promoted cell proliferation and migration. In contrast, knockdown of LINC00470 could significantly inhibit the melanoma cell proliferation and migration, and suppress the growth of tumor in vivo. Overexpression of APEX1 could reverse the impact of the silence of LINC00470 in melanoma cells. In summary, our studies revealed that LINC00470 promoted melanoma proliferation and migration by enhancing the expression of APEX1, which indicated that LINC00470 might be a therapeutic target for the treatment of melanoma. |
format | Online Article Text |
id | pubmed-8055894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80558942021-05-05 LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression Huang, Ting Wang, Yong-Jie Huang, Mi-Tao Guo, Yu Yang, Li-Chang Liu, Xiao-Jin Tan, Wu-Yuan Long, Jian-Hong Cell Death Dis Article Recently studies found that APEX1 was abnormally expressed in melanoma, indicating that it might be involved in the development of melanoma. However, the underlying mechanism and the interaction between APEX1 and LINC00470 in melanoma are not clear. Therefore, we aimed to investigate the role of LINC00470 in the development of melanoma in this work. We discovered that LINC00470 was overexpressed in melanoma tissues and cells compared with the adjacent normal tissues and cells by qPCR. The overexpression of LINC00470 promoted the proliferation and migration of melanoma cells. The functional investigation demonstrated that LINC00470 activated the transcription factor, ZNF131, to regulate the APEX1 expression, which finally promoted cell proliferation and migration. In contrast, knockdown of LINC00470 could significantly inhibit the melanoma cell proliferation and migration, and suppress the growth of tumor in vivo. Overexpression of APEX1 could reverse the impact of the silence of LINC00470 in melanoma cells. In summary, our studies revealed that LINC00470 promoted melanoma proliferation and migration by enhancing the expression of APEX1, which indicated that LINC00470 might be a therapeutic target for the treatment of melanoma. Nature Publishing Group UK 2021-04-19 /pmc/articles/PMC8055894/ /pubmed/33875645 http://dx.doi.org/10.1038/s41419-021-03612-z 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 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 http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Huang, Ting Wang, Yong-Jie Huang, Mi-Tao Guo, Yu Yang, Li-Chang Liu, Xiao-Jin Tan, Wu-Yuan Long, Jian-Hong LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression |
title | LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression |
title_full | LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression |
title_fullStr | LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression |
title_full_unstemmed | LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression |
title_short | LINC00470 accelerates the proliferation and metastasis of melanoma through promoting APEX1 expression |
title_sort | linc00470 accelerates the proliferation and metastasis of melanoma through promoting apex1 expression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8055894/ https://www.ncbi.nlm.nih.gov/pubmed/33875645 http://dx.doi.org/10.1038/s41419-021-03612-z |
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