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MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1

BACKGROUND: Prostate cancer (PCa) is one of the common malignant tumors worldwide. MiR-183-5p has been reported involved in the initiation of human PCa, this study aimed to investigate whether miR-183-5p affects the development of prostate cancer. METHODS: In this study, we analyzed the expression o...

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Autores principales: Feng, Yuehua, Wang, Kai, Qin, Minchao, Zhuang, Qianfeng, Chen, Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334645/
https://www.ncbi.nlm.nih.gov/pubmed/37430206
http://dx.doi.org/10.1186/s12894-023-01286-7
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author Feng, Yuehua
Wang, Kai
Qin, Minchao
Zhuang, Qianfeng
Chen, Zhen
author_facet Feng, Yuehua
Wang, Kai
Qin, Minchao
Zhuang, Qianfeng
Chen, Zhen
author_sort Feng, Yuehua
collection PubMed
description BACKGROUND: Prostate cancer (PCa) is one of the common malignant tumors worldwide. MiR-183-5p has been reported involved in the initiation of human PCa, this study aimed to investigate whether miR-183-5p affects the development of prostate cancer. METHODS: In this study, we analyzed the expression of miR-183-5p in PCa patients and its correlation with clinicopathological parameters based on TCGA data portal. CCK-8, migration assay and invasion and wound-healing assay were performed to detect proliferation, migration and invasion in PCa cells. RESULTS: We found the expression of miR-183-5p was significantly increased in PCa tissues, and high expression of miR-183 was positively associated with poor prognosis of PCa patients. Over-expression of miR-183-5p promoted the migration, invasion capacities of PCa cells, whereas knockdown of miR-183-5p showed reversed function. Furthermore, luciferase reporter assay showed TET1 was identified as a direct target of miR-183-5p, which was negatively correlation with miR-183-5p expression level. Importantly, rescue experiments demonstrated TET1 over-expression could reverse miR-183-5p mimic induced-acceleration of PCa malignant progression. CONCLUSION: Our results indicated that miR-183-5p could act as a tumor promoter in PCa and it accelerated the malignant progression of PCa by directly targeting and down-regulating TET1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12894-023-01286-7.
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spelling pubmed-103346452023-07-12 MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1 Feng, Yuehua Wang, Kai Qin, Minchao Zhuang, Qianfeng Chen, Zhen BMC Urol Research BACKGROUND: Prostate cancer (PCa) is one of the common malignant tumors worldwide. MiR-183-5p has been reported involved in the initiation of human PCa, this study aimed to investigate whether miR-183-5p affects the development of prostate cancer. METHODS: In this study, we analyzed the expression of miR-183-5p in PCa patients and its correlation with clinicopathological parameters based on TCGA data portal. CCK-8, migration assay and invasion and wound-healing assay were performed to detect proliferation, migration and invasion in PCa cells. RESULTS: We found the expression of miR-183-5p was significantly increased in PCa tissues, and high expression of miR-183 was positively associated with poor prognosis of PCa patients. Over-expression of miR-183-5p promoted the migration, invasion capacities of PCa cells, whereas knockdown of miR-183-5p showed reversed function. Furthermore, luciferase reporter assay showed TET1 was identified as a direct target of miR-183-5p, which was negatively correlation with miR-183-5p expression level. Importantly, rescue experiments demonstrated TET1 over-expression could reverse miR-183-5p mimic induced-acceleration of PCa malignant progression. CONCLUSION: Our results indicated that miR-183-5p could act as a tumor promoter in PCa and it accelerated the malignant progression of PCa by directly targeting and down-regulating TET1. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12894-023-01286-7. BioMed Central 2023-07-10 /pmc/articles/PMC10334645/ /pubmed/37430206 http://dx.doi.org/10.1186/s12894-023-01286-7 Text en © The Author(s) 2023 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 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
Feng, Yuehua
Wang, Kai
Qin, Minchao
Zhuang, Qianfeng
Chen, Zhen
MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1
title MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1
title_full MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1
title_fullStr MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1
title_full_unstemmed MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1
title_short MiR-183-5p promotes migration and invasion of prostate cancer by targeting TET1
title_sort mir-183-5p promotes migration and invasion of prostate cancer by targeting tet1
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334645/
https://www.ncbi.nlm.nih.gov/pubmed/37430206
http://dx.doi.org/10.1186/s12894-023-01286-7
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