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Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway
As a common malignant tumor among women, ovarian cancer poses a serious threat to their health. This study demonstrates that long non-coding RNA NRSN2-AS1 is over-expressed in ovarian cancer tissues using patient sample and tissue microarrays. In addition, NRSN2-AS1 is shown to promote ovarian cance...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598275/ https://www.ncbi.nlm.nih.gov/pubmed/37875515 http://dx.doi.org/10.1038/s41419-023-06214-z |
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author | Wu, Yi-Bo Li, Shen-Yi Liu, Jin-Yan Xue, Jia-Jia Xu, Jin-Fu Chen, Ting Cao, Tian-Yue Zhou, Hui Wu, Tian-Tian Dong, Chun-Lin Qian, Wei-Feng Qiao, Long-Wei Hou, Shun-Yu Wang, Ting Shen, Cong |
author_facet | Wu, Yi-Bo Li, Shen-Yi Liu, Jin-Yan Xue, Jia-Jia Xu, Jin-Fu Chen, Ting Cao, Tian-Yue Zhou, Hui Wu, Tian-Tian Dong, Chun-Lin Qian, Wei-Feng Qiao, Long-Wei Hou, Shun-Yu Wang, Ting Shen, Cong |
author_sort | Wu, Yi-Bo |
collection | PubMed |
description | As a common malignant tumor among women, ovarian cancer poses a serious threat to their health. This study demonstrates that long non-coding RNA NRSN2-AS1 is over-expressed in ovarian cancer tissues using patient sample and tissue microarrays. In addition, NRSN2-AS1 is shown to promote ovarian cancer cell proliferation and metastasis both in vitro and in vivo. Mechanistically, NRSN2-AS1 stabilizes protein tyrosine kinase 2 (PTK2) to activate the β-catenin pathway via repressing MG-53-mediated ubiquitinated degradation of PTK2, thereby facilitating ovarian cancer progression. Rescue experiments verify the function of the NRSN2-AS1/PTK2/β-catenin axis and the effects of MG53 on this axis in ovarian cancer cells. In conclusion, this study demonstrates the key role of the NRSN2-AS1/PTK2/β-catenin axis for the first time and explores its potential clinical applications in ovarian cancer. |
format | Online Article Text |
id | pubmed-10598275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105982752023-10-26 Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway Wu, Yi-Bo Li, Shen-Yi Liu, Jin-Yan Xue, Jia-Jia Xu, Jin-Fu Chen, Ting Cao, Tian-Yue Zhou, Hui Wu, Tian-Tian Dong, Chun-Lin Qian, Wei-Feng Qiao, Long-Wei Hou, Shun-Yu Wang, Ting Shen, Cong Cell Death Dis Article As a common malignant tumor among women, ovarian cancer poses a serious threat to their health. This study demonstrates that long non-coding RNA NRSN2-AS1 is over-expressed in ovarian cancer tissues using patient sample and tissue microarrays. In addition, NRSN2-AS1 is shown to promote ovarian cancer cell proliferation and metastasis both in vitro and in vivo. Mechanistically, NRSN2-AS1 stabilizes protein tyrosine kinase 2 (PTK2) to activate the β-catenin pathway via repressing MG-53-mediated ubiquitinated degradation of PTK2, thereby facilitating ovarian cancer progression. Rescue experiments verify the function of the NRSN2-AS1/PTK2/β-catenin axis and the effects of MG53 on this axis in ovarian cancer cells. In conclusion, this study demonstrates the key role of the NRSN2-AS1/PTK2/β-catenin axis for the first time and explores its potential clinical applications in ovarian cancer. Nature Publishing Group UK 2023-10-24 /pmc/articles/PMC10598275/ /pubmed/37875515 http://dx.doi.org/10.1038/s41419-023-06214-z Text en © The Author(s) 2023 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 Wu, Yi-Bo Li, Shen-Yi Liu, Jin-Yan Xue, Jia-Jia Xu, Jin-Fu Chen, Ting Cao, Tian-Yue Zhou, Hui Wu, Tian-Tian Dong, Chun-Lin Qian, Wei-Feng Qiao, Long-Wei Hou, Shun-Yu Wang, Ting Shen, Cong Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway |
title | Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway |
title_full | Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway |
title_fullStr | Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway |
title_full_unstemmed | Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway |
title_short | Long non-coding RNA NRSN2-AS1 promotes ovarian cancer progression through targeting PTK2/β-catenin pathway |
title_sort | long non-coding rna nrsn2-as1 promotes ovarian cancer progression through targeting ptk2/β-catenin pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598275/ https://www.ncbi.nlm.nih.gov/pubmed/37875515 http://dx.doi.org/10.1038/s41419-023-06214-z |
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