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miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9

Previous studies have revealed that miRNAs participate in the pathogenesis of ovarian cancer; however, whether miR-600 is also involved remains unclear. In this study, we aimed to investigated the role of miR-600 in ovarian cancer progression. Here, miR-600 expression was significantly upregulated i...

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Autores principales: Shan, Lili, Song, Pingping, Zhao, Yangyang, An, Na, Xia, Yanqiu, Qi, Yue, Zhao, Hongyan, Ge, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063371/
https://www.ncbi.nlm.nih.gov/pubmed/35501825
http://dx.doi.org/10.1186/s13048-022-00981-7
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author Shan, Lili
Song, Pingping
Zhao, Yangyang
An, Na
Xia, Yanqiu
Qi, Yue
Zhao, Hongyan
Ge, Jing
author_facet Shan, Lili
Song, Pingping
Zhao, Yangyang
An, Na
Xia, Yanqiu
Qi, Yue
Zhao, Hongyan
Ge, Jing
author_sort Shan, Lili
collection PubMed
description Previous studies have revealed that miRNAs participate in the pathogenesis of ovarian cancer; however, whether miR-600 is also involved remains unclear. In this study, we aimed to investigated the role of miR-600 in ovarian cancer progression. Here, miR-600 expression was significantly upregulated in ovarian cancer tissues and stem cells. Functional studies showed that miR-600 promoted ovarian cancer cell stemness, proliferation and metastasis. Mechanistic studies revealed that Kruppel like factor 9 (KLF9) was indicated as the target of miR-600. The luciferase reporter assay suggested that miR-600 directly bound to the 3′-untranslated region of KLF9. Additionally, miR-600 expression was negatively associated with KLF9 expression in human ovarian cancer tissues. Si-KLF9 partially abolished the discrepancy of self-renewal, growth and metastasis capacity between miR-600 knockdown ovarian cancer cells and control cells. In conclusion, our results suggest that miR-600 promotes ovarian cancer cell stemness, proliferation and metastasis via directly downregulating KLF9, and impairing miR-600 levels may be a new treatment strategy for ovarian cancer in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13048-022-00981-7.
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spelling pubmed-90633712022-05-04 miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9 Shan, Lili Song, Pingping Zhao, Yangyang An, Na Xia, Yanqiu Qi, Yue Zhao, Hongyan Ge, Jing J Ovarian Res Research Previous studies have revealed that miRNAs participate in the pathogenesis of ovarian cancer; however, whether miR-600 is also involved remains unclear. In this study, we aimed to investigated the role of miR-600 in ovarian cancer progression. Here, miR-600 expression was significantly upregulated in ovarian cancer tissues and stem cells. Functional studies showed that miR-600 promoted ovarian cancer cell stemness, proliferation and metastasis. Mechanistic studies revealed that Kruppel like factor 9 (KLF9) was indicated as the target of miR-600. The luciferase reporter assay suggested that miR-600 directly bound to the 3′-untranslated region of KLF9. Additionally, miR-600 expression was negatively associated with KLF9 expression in human ovarian cancer tissues. Si-KLF9 partially abolished the discrepancy of self-renewal, growth and metastasis capacity between miR-600 knockdown ovarian cancer cells and control cells. In conclusion, our results suggest that miR-600 promotes ovarian cancer cell stemness, proliferation and metastasis via directly downregulating KLF9, and impairing miR-600 levels may be a new treatment strategy for ovarian cancer in the future. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13048-022-00981-7. BioMed Central 2022-05-03 /pmc/articles/PMC9063371/ /pubmed/35501825 http://dx.doi.org/10.1186/s13048-022-00981-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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, visithttp://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
Shan, Lili
Song, Pingping
Zhao, Yangyang
An, Na
Xia, Yanqiu
Qi, Yue
Zhao, Hongyan
Ge, Jing
miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9
title miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9
title_full miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9
title_fullStr miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9
title_full_unstemmed miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9
title_short miR-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting KLF9
title_sort mir-600 promotes ovarian cancer cells stemness, proliferation and metastasis via targeting klf9
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063371/
https://www.ncbi.nlm.nih.gov/pubmed/35501825
http://dx.doi.org/10.1186/s13048-022-00981-7
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