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Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis
BACKGROUND: X inactivation-specific transcript (XIST) is the long non-coding RNA (lncRNA) related to cancer, which is involved in the development and progression of various types of tumor. However, up to now, the exact role and molecular mechanism of XIST in the progression of ovarian cancer are not...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180121/ https://www.ncbi.nlm.nih.gov/pubmed/34090463 http://dx.doi.org/10.1186/s12957-021-02274-7 |
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author | Meng, Qingjuan Wang, Ningning Duan, Guanglan |
author_facet | Meng, Qingjuan Wang, Ningning Duan, Guanglan |
author_sort | Meng, Qingjuan |
collection | PubMed |
description | BACKGROUND: X inactivation-specific transcript (XIST) is the long non-coding RNA (lncRNA) related to cancer, which is involved in the development and progression of various types of tumor. However, up to now, the exact role and molecular mechanism of XIST in the progression of ovarian cancer are not clear. We studied the function of XIST in ovarian cancer cells and clinical tumor specimens. METHODS: RT-qPCR was performed to detect the expression levels of miR-335 and BCL2L2 in ovarian cancer cells and tissues. MTT and transwell assays were carried out to detect cell proliferation, migration, and invasion abilities. Western blot was performed to analyze the expression level of BCL2L2. The interaction between miR-335 and XIST/BCL2L2 was confirmed using a luciferase reporter assay. RESULTS: The inhibition of XIST can inhibit the proliferation invasion and migration of human ovarian cancer cells. In addition, the miR-335/BCL2L2 axis was involved in the functions of XIST in ovarian cancer cells. These results suggested that XIST could regulate tumor proliferation and invasion and migration via modulating miR-335/BCL2L2. CONCLUSION: XIST might be a carcinogenic lncRNA in ovarian cancer by regulating miR-335, and it can serve as a therapeutic target in human ovarian cancer. |
format | Online Article Text |
id | pubmed-8180121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81801212021-06-07 Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis Meng, Qingjuan Wang, Ningning Duan, Guanglan World J Surg Oncol Research BACKGROUND: X inactivation-specific transcript (XIST) is the long non-coding RNA (lncRNA) related to cancer, which is involved in the development and progression of various types of tumor. However, up to now, the exact role and molecular mechanism of XIST in the progression of ovarian cancer are not clear. We studied the function of XIST in ovarian cancer cells and clinical tumor specimens. METHODS: RT-qPCR was performed to detect the expression levels of miR-335 and BCL2L2 in ovarian cancer cells and tissues. MTT and transwell assays were carried out to detect cell proliferation, migration, and invasion abilities. Western blot was performed to analyze the expression level of BCL2L2. The interaction between miR-335 and XIST/BCL2L2 was confirmed using a luciferase reporter assay. RESULTS: The inhibition of XIST can inhibit the proliferation invasion and migration of human ovarian cancer cells. In addition, the miR-335/BCL2L2 axis was involved in the functions of XIST in ovarian cancer cells. These results suggested that XIST could regulate tumor proliferation and invasion and migration via modulating miR-335/BCL2L2. CONCLUSION: XIST might be a carcinogenic lncRNA in ovarian cancer by regulating miR-335, and it can serve as a therapeutic target in human ovarian cancer. BioMed Central 2021-06-05 /pmc/articles/PMC8180121/ /pubmed/34090463 http://dx.doi.org/10.1186/s12957-021-02274-7 Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Meng, Qingjuan Wang, Ningning Duan, Guanglan Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis |
title | Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis |
title_full | Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis |
title_fullStr | Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis |
title_full_unstemmed | Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis |
title_short | Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis |
title_sort | long non-coding rna xist regulates ovarian cancer progression via modulating mir-335/bcl2l2 axis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180121/ https://www.ncbi.nlm.nih.gov/pubmed/34090463 http://dx.doi.org/10.1186/s12957-021-02274-7 |
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