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LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis
BACKGROUND: Long non-coding RNA (lncRNA) exhibits a crucial role in multiple human malignancies. The expression of lncRNA LINC00511, reportedly, is aberrantly up-regulated in several types of tumors. Our research was aimed at deciphering the role and mechanism of LINC00511 in the progression of cerv...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617969/ https://www.ncbi.nlm.nih.gov/pubmed/36103025 http://dx.doi.org/10.1007/s10495-022-01768-3 |
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author | Lu, Mingming Gao, Qing Wang, Yafei Ren, Jie Zhang, Tingting |
author_facet | Lu, Mingming Gao, Qing Wang, Yafei Ren, Jie Zhang, Tingting |
author_sort | Lu, Mingming |
collection | PubMed |
description | BACKGROUND: Long non-coding RNA (lncRNA) exhibits a crucial role in multiple human malignancies. The expression of lncRNA LINC00511, reportedly, is aberrantly up-regulated in several types of tumors. Our research was aimed at deciphering the role and mechanism of LINC00511 in the progression of cervical cancer (CC). METHOD: Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to quantify the expression levels of LINC00511, miR-497-5p and MAPK1 mRNA in CC tissues and cell lines. Cell counting kit-8 (CCK-8), 5-bromo-2’-deoxyuridine (BrdU) and Transwell assays were conducted for detecting the proliferation, migration and invasion of CC cells. Dual-luciferase reporter gene experiments were performed to verify the targeting relationships amongst LINC00511, miR-497-5p and MAPK1. Besides, MAPK1 expression in CC cells was detected via Western blot after LINC00511 and miR-497-5p were selectively regulated. RESULTS: Up-regulation of LINC00511 expression in CC tissues and cell lines was observed, which was in association with tumor size, clinical stage and lymph node metastasis of the patients. LINC00511 overexpression facilitated the proliferation, migration and invasion of CC cells, while opposite effects were observed after knockdown of LINC00511. Mechanistically, LINC00511 was capable of targeting miR-497-5p and up-regulating MAPK1 expression. CONCLUSION: LINC00511/miR-497-5p/MAPK1 axis regulates CC progression. |
format | Online Article Text |
id | pubmed-9617969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-96179692022-10-31 LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis Lu, Mingming Gao, Qing Wang, Yafei Ren, Jie Zhang, Tingting Apoptosis Article BACKGROUND: Long non-coding RNA (lncRNA) exhibits a crucial role in multiple human malignancies. The expression of lncRNA LINC00511, reportedly, is aberrantly up-regulated in several types of tumors. Our research was aimed at deciphering the role and mechanism of LINC00511 in the progression of cervical cancer (CC). METHOD: Quantitative real-time polymerase chain reaction (qRT-PCR) was performed to quantify the expression levels of LINC00511, miR-497-5p and MAPK1 mRNA in CC tissues and cell lines. Cell counting kit-8 (CCK-8), 5-bromo-2’-deoxyuridine (BrdU) and Transwell assays were conducted for detecting the proliferation, migration and invasion of CC cells. Dual-luciferase reporter gene experiments were performed to verify the targeting relationships amongst LINC00511, miR-497-5p and MAPK1. Besides, MAPK1 expression in CC cells was detected via Western blot after LINC00511 and miR-497-5p were selectively regulated. RESULTS: Up-regulation of LINC00511 expression in CC tissues and cell lines was observed, which was in association with tumor size, clinical stage and lymph node metastasis of the patients. LINC00511 overexpression facilitated the proliferation, migration and invasion of CC cells, while opposite effects were observed after knockdown of LINC00511. Mechanistically, LINC00511 was capable of targeting miR-497-5p and up-regulating MAPK1 expression. CONCLUSION: LINC00511/miR-497-5p/MAPK1 axis regulates CC progression. Springer US 2022-09-14 2022 /pmc/articles/PMC9617969/ /pubmed/36103025 http://dx.doi.org/10.1007/s10495-022-01768-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lu, Mingming Gao, Qing Wang, Yafei Ren, Jie Zhang, Tingting LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis |
title | LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis |
title_full | LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis |
title_fullStr | LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis |
title_full_unstemmed | LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis |
title_short | LINC00511 promotes cervical cancer progression by regulating the miR-497-5p/MAPK1 axis |
title_sort | linc00511 promotes cervical cancer progression by regulating the mir-497-5p/mapk1 axis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617969/ https://www.ncbi.nlm.nih.gov/pubmed/36103025 http://dx.doi.org/10.1007/s10495-022-01768-3 |
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