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Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the Proliferation of Colorectal Cancer
BACKGROUND: LBX2 antisense RNA 1 (LBX2-AS1), a long noncoding RNA, has been identified to be closely associated with the progression of various cancers. However, the role of LBX2-AS1 in colorectal cancer (CRC) is still poorly understood. In this study, we aimed to investigate the expression and func...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983235/ https://www.ncbi.nlm.nih.gov/pubmed/33733923 http://dx.doi.org/10.1177/1533033821997829 |
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author | Li, Qing Xie, Hui Jin, Zefu Huang, Jing Wang, Shuting Zhang, Zijian |
author_facet | Li, Qing Xie, Hui Jin, Zefu Huang, Jing Wang, Shuting Zhang, Zijian |
author_sort | Li, Qing |
collection | PubMed |
description | BACKGROUND: LBX2 antisense RNA 1 (LBX2-AS1), a long noncoding RNA, has been identified to be closely associated with the progression of various cancers. However, the role of LBX2-AS1 in colorectal cancer (CRC) is still poorly understood. In this study, we aimed to investigate the expression and function of LBX2-AS1 in CRC. MATERIAL AND METHODS: Expression data from the Gene Expression Omnibus (GEO) and Gene Expression Profiling Interactive Analysis (GEPIA) databases and results obtained from clinical samples/patients were used to determine the correlation between LBX2-AS1 expression and pathological stages, overall survival (OS). Furthermore, knockdown of LBX2-AS1 in CRC cells using the short interfering RNA (siRNA) technique, and observed its biological functions using western blotting, quantitative reverse transcription-polymerase chain reaction (qRT-PCR), cell counting kit-8 (CCK-8) and flow cytometry assay in the CRC cell line. RESULTS: Our study demonstrated that the expression levels of LBX2-AS1 were higher in CRC cell lines than in normal colon mucosal cell lines. Bioinformatics analysis revealed that CRC patients with high LBX2-AS1 expression levels had poor OS. Furthermore, knockdown of LBX2-AS1 in CRC cells could attenuate the proliferative ability of CRC cells in vitro, which is associated with decreased expression of cyclin-dependent kinase (CDK) 3, CDK6, and CCND1 and enhanced expression of cyclin-dependent kinase inhibitor 1A. CONCLUSIONS: LBX2-AS1 plays a crucial role in the tumorigenesis of CRC, providing a potential therapeutic target for CRC patients. |
format | Online Article Text |
id | pubmed-7983235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79832352021-03-31 Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the Proliferation of Colorectal Cancer Li, Qing Xie, Hui Jin, Zefu Huang, Jing Wang, Shuting Zhang, Zijian Technol Cancer Res Treat Original Article BACKGROUND: LBX2 antisense RNA 1 (LBX2-AS1), a long noncoding RNA, has been identified to be closely associated with the progression of various cancers. However, the role of LBX2-AS1 in colorectal cancer (CRC) is still poorly understood. In this study, we aimed to investigate the expression and function of LBX2-AS1 in CRC. MATERIAL AND METHODS: Expression data from the Gene Expression Omnibus (GEO) and Gene Expression Profiling Interactive Analysis (GEPIA) databases and results obtained from clinical samples/patients were used to determine the correlation between LBX2-AS1 expression and pathological stages, overall survival (OS). Furthermore, knockdown of LBX2-AS1 in CRC cells using the short interfering RNA (siRNA) technique, and observed its biological functions using western blotting, quantitative reverse transcription-polymerase chain reaction (qRT-PCR), cell counting kit-8 (CCK-8) and flow cytometry assay in the CRC cell line. RESULTS: Our study demonstrated that the expression levels of LBX2-AS1 were higher in CRC cell lines than in normal colon mucosal cell lines. Bioinformatics analysis revealed that CRC patients with high LBX2-AS1 expression levels had poor OS. Furthermore, knockdown of LBX2-AS1 in CRC cells could attenuate the proliferative ability of CRC cells in vitro, which is associated with decreased expression of cyclin-dependent kinase (CDK) 3, CDK6, and CCND1 and enhanced expression of cyclin-dependent kinase inhibitor 1A. CONCLUSIONS: LBX2-AS1 plays a crucial role in the tumorigenesis of CRC, providing a potential therapeutic target for CRC patients. SAGE Publications 2021-03-18 /pmc/articles/PMC7983235/ /pubmed/33733923 http://dx.doi.org/10.1177/1533033821997829 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Li, Qing Xie, Hui Jin, Zefu Huang, Jing Wang, Shuting Zhang, Zijian Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the Proliferation of Colorectal Cancer |
title | Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the
Proliferation of Colorectal Cancer |
title_full | Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the
Proliferation of Colorectal Cancer |
title_fullStr | Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the
Proliferation of Colorectal Cancer |
title_full_unstemmed | Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the
Proliferation of Colorectal Cancer |
title_short | Overexpression of Long Noncoding RNA LBX2-AS1 Promotes the
Proliferation of Colorectal Cancer |
title_sort | overexpression of long noncoding rna lbx2-as1 promotes the
proliferation of colorectal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983235/ https://www.ncbi.nlm.nih.gov/pubmed/33733923 http://dx.doi.org/10.1177/1533033821997829 |
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