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Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B
GPNCA is a long non-coding RNA with unknown functions. In this study, using data from 9 cancers obtained from The Cancer Genome Atlas (TCGA), GPNCA was identified as overexpressed in cancer vs. normal tissues. The upregulation of GPNCA was associated with poor overall prognosis in colon, liver, rena...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004998/ https://www.ncbi.nlm.nih.gov/pubmed/32029792 http://dx.doi.org/10.1038/s41598-020-58729-6 |
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author | Liao, Weijie Liu, Fuhai Zhang, Haowei Liao, Weifang Xu, Naihan Xie, Weidong Zhang, Yaou |
author_facet | Liao, Weijie Liu, Fuhai Zhang, Haowei Liao, Weifang Xu, Naihan Xie, Weidong Zhang, Yaou |
author_sort | Liao, Weijie |
collection | PubMed |
description | GPNCA is a long non-coding RNA with unknown functions. In this study, using data from 9 cancers obtained from The Cancer Genome Atlas (TCGA), GPNCA was identified as overexpressed in cancer vs. normal tissues. The upregulation of GPNCA was associated with poor overall prognosis in colon, liver, renal clear cell and breast cancers. The upregulation of GPNCA was partly due to enhanced H3K27ac occupancy on its promoter region via EP300 and KAT2A/GCN5. The overexpression of GPNCA was positively related to tumor metastasis in colon cancer and poor disease-free and recurrence-free survival in colon and liver cancer. Both gene ontology (GO) enrichment and Kyoto encyclopedia of genes and genomes (KEGG) pathway enrichment analysis indicated that GPNCA was closely linked to regulation of gene transcription and post-transcriptional modifications, which was further supported by in vitro cell cytoplasmic and nuclear RNA purification assessments. Furthermore, GPNCA was associated with cell growth. Our in vitro experiments demonstrated that GPNCA silencing inhibited tumor growth via inhibiting its nearby gene GSK3B. Taken together, these findings highlight GPNCA as a biomarker for cancer diagnosis and a potential target for future cancer drug development. |
format | Online Article Text |
id | pubmed-7004998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70049982020-02-14 Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B Liao, Weijie Liu, Fuhai Zhang, Haowei Liao, Weifang Xu, Naihan Xie, Weidong Zhang, Yaou Sci Rep Article GPNCA is a long non-coding RNA with unknown functions. In this study, using data from 9 cancers obtained from The Cancer Genome Atlas (TCGA), GPNCA was identified as overexpressed in cancer vs. normal tissues. The upregulation of GPNCA was associated with poor overall prognosis in colon, liver, renal clear cell and breast cancers. The upregulation of GPNCA was partly due to enhanced H3K27ac occupancy on its promoter region via EP300 and KAT2A/GCN5. The overexpression of GPNCA was positively related to tumor metastasis in colon cancer and poor disease-free and recurrence-free survival in colon and liver cancer. Both gene ontology (GO) enrichment and Kyoto encyclopedia of genes and genomes (KEGG) pathway enrichment analysis indicated that GPNCA was closely linked to regulation of gene transcription and post-transcriptional modifications, which was further supported by in vitro cell cytoplasmic and nuclear RNA purification assessments. Furthermore, GPNCA was associated with cell growth. Our in vitro experiments demonstrated that GPNCA silencing inhibited tumor growth via inhibiting its nearby gene GSK3B. Taken together, these findings highlight GPNCA as a biomarker for cancer diagnosis and a potential target for future cancer drug development. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7004998/ /pubmed/32029792 http://dx.doi.org/10.1038/s41598-020-58729-6 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Liao, Weijie Liu, Fuhai Zhang, Haowei Liao, Weifang Xu, Naihan Xie, Weidong Zhang, Yaou Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B |
title | Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B |
title_full | Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B |
title_fullStr | Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B |
title_full_unstemmed | Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B |
title_short | Upregulation of GPNCA is associated with poor prognosis through enhancement of tumor growth via regulating GSK3B |
title_sort | upregulation of gpnca is associated with poor prognosis through enhancement of tumor growth via regulating gsk3b |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004998/ https://www.ncbi.nlm.nih.gov/pubmed/32029792 http://dx.doi.org/10.1038/s41598-020-58729-6 |
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