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Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression
PURPOSE: miRNAs can act as oncogenes or tumor suppressors and participate in the development and progression of tumors, thus affecting the prognosis and survival of cancer patients. In this paper, we mainly studied the role of miR-1826 in prostate cancer. PATIENTS AND METHODS: The expression of miR-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370600/ https://www.ncbi.nlm.nih.gov/pubmed/34413652 http://dx.doi.org/10.2147/OTT.S295125 |
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author | Liu, Yongguo Liu, Jing Han, Xiancheng Mou, Linkai |
author_facet | Liu, Yongguo Liu, Jing Han, Xiancheng Mou, Linkai |
author_sort | Liu, Yongguo |
collection | PubMed |
description | PURPOSE: miRNAs can act as oncogenes or tumor suppressors and participate in the development and progression of tumors, thus affecting the prognosis and survival of cancer patients. In this paper, we mainly studied the role of miR-1826 in prostate cancer. PATIENTS AND METHODS: The expression of miR-1826 was studied by quantitative real-time PCR (qRT-PCR). Kaplan–Meier curves were used to analyze the relationship between the expression of miR-1826 and the survival rate of PC patients. Cox regression analysis was used to study the risk factors affecting the prognosis of PC patients. PC cells were transfected with miR-1826 mimic, mimic negative control (mimic NC), miR-1826 inhibitor, or inhibitor NC. The effect of miR-1826 on the proliferation of PC cells was studied by the CCK-8 method and colony formation assay. Transwell assays were used to detect the effect of miR-1826 on the migratory and invasive abilities of tumor cells. RESULTS: The expression of miR-1826 in PC tissues was lower than that in adjacent normal tissues, and that the expression levels of miR-1826 in four PC cell lines were all lower than normal human prostate epithelial cell lines. Patients with low expression of miR-1826 had shorter overall survival compared with those with high expression. The downregulation of miR-1826 promoted PC cell proliferation, migration, and invasion. CONCLUSION: In summary, the low expression of miR-1826 may promote the progression of PC, and the low expression of miR-1826 is also associated with a poor prognosis in PC patients. |
format | Online Article Text |
id | pubmed-8370600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-83706002021-08-18 Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression Liu, Yongguo Liu, Jing Han, Xiancheng Mou, Linkai Onco Targets Ther Original Research PURPOSE: miRNAs can act as oncogenes or tumor suppressors and participate in the development and progression of tumors, thus affecting the prognosis and survival of cancer patients. In this paper, we mainly studied the role of miR-1826 in prostate cancer. PATIENTS AND METHODS: The expression of miR-1826 was studied by quantitative real-time PCR (qRT-PCR). Kaplan–Meier curves were used to analyze the relationship between the expression of miR-1826 and the survival rate of PC patients. Cox regression analysis was used to study the risk factors affecting the prognosis of PC patients. PC cells were transfected with miR-1826 mimic, mimic negative control (mimic NC), miR-1826 inhibitor, or inhibitor NC. The effect of miR-1826 on the proliferation of PC cells was studied by the CCK-8 method and colony formation assay. Transwell assays were used to detect the effect of miR-1826 on the migratory and invasive abilities of tumor cells. RESULTS: The expression of miR-1826 in PC tissues was lower than that in adjacent normal tissues, and that the expression levels of miR-1826 in four PC cell lines were all lower than normal human prostate epithelial cell lines. Patients with low expression of miR-1826 had shorter overall survival compared with those with high expression. The downregulation of miR-1826 promoted PC cell proliferation, migration, and invasion. CONCLUSION: In summary, the low expression of miR-1826 may promote the progression of PC, and the low expression of miR-1826 is also associated with a poor prognosis in PC patients. Dove 2021-08-13 /pmc/articles/PMC8370600/ /pubmed/34413652 http://dx.doi.org/10.2147/OTT.S295125 Text en © 2021 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Liu, Yongguo Liu, Jing Han, Xiancheng Mou, Linkai Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression |
title | Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression |
title_full | Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression |
title_fullStr | Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression |
title_full_unstemmed | Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression |
title_short | Prognostic Value of miR-1826 in Prostate Cancer and Its Regulatory Effect on Tumor Progression |
title_sort | prognostic value of mir-1826 in prostate cancer and its regulatory effect on tumor progression |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370600/ https://www.ncbi.nlm.nih.gov/pubmed/34413652 http://dx.doi.org/10.2147/OTT.S295125 |
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