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Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis
Gastric cancer (GC) is a global health problem and further studies of its molecular mechanisms are needed to identify effective therapeutic targets. Although some long noncoding RNAs (lncRNAs) have been found to be involved in the progression of GC, the molecular mechanisms of many GC-related lncRNA...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752798/ https://www.ncbi.nlm.nih.gov/pubmed/35017465 http://dx.doi.org/10.1038/s41420-021-00809-1 |
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author | Ma, Xiang Wang, Gang Fan, Hao Li, Zengliang Chen, Wangwang Xiao, Jian Ni, Peidong Liu, Kanghui Shen, Kuan Wang, Yuanhang Xu, Zekuan Yang, Li |
author_facet | Ma, Xiang Wang, Gang Fan, Hao Li, Zengliang Chen, Wangwang Xiao, Jian Ni, Peidong Liu, Kanghui Shen, Kuan Wang, Yuanhang Xu, Zekuan Yang, Li |
author_sort | Ma, Xiang |
collection | PubMed |
description | Gastric cancer (GC) is a global health problem and further studies of its molecular mechanisms are needed to identify effective therapeutic targets. Although some long noncoding RNAs (lncRNAs) have been found to be involved in the progression of GC, the molecular mechanisms of many GC-related lncRNAs remain unclear. In this study, a series of in vivo and in vitro assays were performed to study the relationship between FAM225A and GC, which showed that FAM225A levels were correlated with poor prognosis in GC. Higher FAM225A expression tended to be correlated with a more profound lymphatic metastasis rate, larger tumor size, and more advanced tumor stage. FAM225A also promoted gastric cell proliferation, invasion, and migration. Further mechanistic investigation showed that FAM225A acted as a miR-326 sponge to upregulate its direct target PADI2 in GC. Overall, our findings indicated that FAM225A promoted GC development and progression via a competitive endogenous RNA network of FAM225A/miR-326/PADI2 in GC, providing insight into possible therapeutic targets and prognosis of GC. |
format | Online Article Text |
id | pubmed-8752798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87527982022-01-20 Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis Ma, Xiang Wang, Gang Fan, Hao Li, Zengliang Chen, Wangwang Xiao, Jian Ni, Peidong Liu, Kanghui Shen, Kuan Wang, Yuanhang Xu, Zekuan Yang, Li Cell Death Discov Article Gastric cancer (GC) is a global health problem and further studies of its molecular mechanisms are needed to identify effective therapeutic targets. Although some long noncoding RNAs (lncRNAs) have been found to be involved in the progression of GC, the molecular mechanisms of many GC-related lncRNAs remain unclear. In this study, a series of in vivo and in vitro assays were performed to study the relationship between FAM225A and GC, which showed that FAM225A levels were correlated with poor prognosis in GC. Higher FAM225A expression tended to be correlated with a more profound lymphatic metastasis rate, larger tumor size, and more advanced tumor stage. FAM225A also promoted gastric cell proliferation, invasion, and migration. Further mechanistic investigation showed that FAM225A acted as a miR-326 sponge to upregulate its direct target PADI2 in GC. Overall, our findings indicated that FAM225A promoted GC development and progression via a competitive endogenous RNA network of FAM225A/miR-326/PADI2 in GC, providing insight into possible therapeutic targets and prognosis of GC. Nature Publishing Group UK 2022-01-11 /pmc/articles/PMC8752798/ /pubmed/35017465 http://dx.doi.org/10.1038/s41420-021-00809-1 Text en © The Author(s) 2022 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 Ma, Xiang Wang, Gang Fan, Hao Li, Zengliang Chen, Wangwang Xiao, Jian Ni, Peidong Liu, Kanghui Shen, Kuan Wang, Yuanhang Xu, Zekuan Yang, Li Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis |
title | Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis |
title_full | Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis |
title_fullStr | Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis |
title_full_unstemmed | Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis |
title_short | Long noncoding RNA FAM225A promotes the malignant progression of gastric cancer through the miR-326/PADI2 axis |
title_sort | long noncoding rna fam225a promotes the malignant progression of gastric cancer through the mir-326/padi2 axis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8752798/ https://www.ncbi.nlm.nih.gov/pubmed/35017465 http://dx.doi.org/10.1038/s41420-021-00809-1 |
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