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Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells
Dynamin 3 (DNM3) functions as a tumor suppressor in various malignancies. However, the underlying mechanism of DNM3 in cervical cancer remains to be elucidated. The present study aimed to indicate the function of DNM3 in cervical cancer. The expression of DNM3 in cervical tissues and cells was measu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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D.A. Spandidos
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130055/ https://www.ncbi.nlm.nih.gov/pubmed/34025791 http://dx.doi.org/10.3892/ol.2021.12785 |
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author | Fa, Jing |
author_facet | Fa, Jing |
author_sort | Fa, Jing |
collection | PubMed |
description | Dynamin 3 (DNM3) functions as a tumor suppressor in various malignancies. However, the underlying mechanism of DNM3 in cervical cancer remains to be elucidated. The present study aimed to indicate the function of DNM3 in cervical cancer. The expression of DNM3 in cervical tissues and cells was measured using bioinformatics analysis, immunohistochemistry and reverse transcription-quantitative PCR. The pcDNA3.1 plasmid was used to overexpress DNM3 in SiHa and C33A cells. The effects of DNM3 overexpression on cell proliferation, migration, invasion and apoptosis was detected by the CCK-8, clone formation, Transwell, flow cytometry and western blotting assays. In the present study, it was revealed that DNM3 was expressed at significantly low levels in cervical cancer tissues and cell lines compared with normal cervical tissues and cell lines. In addition, the low expression of DNM3 was significantly associated with high pathological grading of cervical cancer. The overall survival rate of patients with low DNM3 expression was significantly improved compared with patients with high DNM3 expression. In addition, the overexpression of DNM3 significantly inhibited the proliferation, migration and invasion of cervical carcinoma cells and induced cell apoptosis. The findings of the present study further revealed that the overexpression of DNM3 may inhibit cell migration and invasion by inactivating the epithelial mesenchymal transition process. In summary, the present study demonstrated that DNM3 was a tumor suppressor in cervical cancer progression and that it may serve as a potential prognostic biomarker for patients with cervical carcinoma. |
format | Online Article Text |
id | pubmed-8130055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-81300552021-05-21 Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells Fa, Jing Oncol Lett Articles Dynamin 3 (DNM3) functions as a tumor suppressor in various malignancies. However, the underlying mechanism of DNM3 in cervical cancer remains to be elucidated. The present study aimed to indicate the function of DNM3 in cervical cancer. The expression of DNM3 in cervical tissues and cells was measured using bioinformatics analysis, immunohistochemistry and reverse transcription-quantitative PCR. The pcDNA3.1 plasmid was used to overexpress DNM3 in SiHa and C33A cells. The effects of DNM3 overexpression on cell proliferation, migration, invasion and apoptosis was detected by the CCK-8, clone formation, Transwell, flow cytometry and western blotting assays. In the present study, it was revealed that DNM3 was expressed at significantly low levels in cervical cancer tissues and cell lines compared with normal cervical tissues and cell lines. In addition, the low expression of DNM3 was significantly associated with high pathological grading of cervical cancer. The overall survival rate of patients with low DNM3 expression was significantly improved compared with patients with high DNM3 expression. In addition, the overexpression of DNM3 significantly inhibited the proliferation, migration and invasion of cervical carcinoma cells and induced cell apoptosis. The findings of the present study further revealed that the overexpression of DNM3 may inhibit cell migration and invasion by inactivating the epithelial mesenchymal transition process. In summary, the present study demonstrated that DNM3 was a tumor suppressor in cervical cancer progression and that it may serve as a potential prognostic biomarker for patients with cervical carcinoma. D.A. Spandidos 2021-07 2021-05-12 /pmc/articles/PMC8130055/ /pubmed/34025791 http://dx.doi.org/10.3892/ol.2021.12785 Text en Copyright: © Fa et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Fa, Jing Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
title | Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
title_full | Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
title_fullStr | Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
title_full_unstemmed | Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
title_short | Dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
title_sort | dynamin 3 overexpression suppresses the proliferation, migration and invasion of cervical cancer cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130055/ https://www.ncbi.nlm.nih.gov/pubmed/34025791 http://dx.doi.org/10.3892/ol.2021.12785 |
work_keys_str_mv | AT fajing dynamin3overexpressionsuppressestheproliferationmigrationandinvasionofcervicalcancercells |