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MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells
OBJECTIVE: The activity of NEK6 is enhanced in several cancer cells, including colon adenocarcinoma (COAD) cells. However, there are few reports on the microRNA (miRNA/miR) regulation of NEK6. In this study, we aimed to investigate the effects of miRNAs targeting NEK6 in COAD cells. METHODS: Public...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791743/ https://www.ncbi.nlm.nih.gov/pubmed/35096064 http://dx.doi.org/10.1155/2022/7007718 |
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author | Hong, Zhongshi Chen, Zhichuan Pan, Jianpeng Shi, Zesheng Wang, Chunxiao Qiu, Chengzhi |
author_facet | Hong, Zhongshi Chen, Zhichuan Pan, Jianpeng Shi, Zesheng Wang, Chunxiao Qiu, Chengzhi |
author_sort | Hong, Zhongshi |
collection | PubMed |
description | OBJECTIVE: The activity of NEK6 is enhanced in several cancer cells, including colon adenocarcinoma (COAD) cells. However, there are few reports on the microRNA (miRNA/miR) regulation of NEK6. In this study, we aimed to investigate the effects of miRNAs targeting NEK6 in COAD cells. METHODS: Public data and online analysis sites were used to analyze the expression levels of NEK6 and miR-323a-3p in COAD tissues as well as the relationship between NEK6 or miR-323a-3p levels and survival in patients with COAD and to predict miRNAs targeting NEK6. Real-time polymerase chain reaction and western blotting were performed to determine the levels of NEK6 and miR-323a-3p in COAD cells. The targeting of NEK6 by miR-323a-3p was verified using a dual-luciferase reporter assay. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, 5-ethynyl-2′-deoxyuridine assay, propidium iodide (PI) staining, annexin V-fluorescein isothiocyanate/PI staining, and transwell assay were employed to test the proliferation, apoptosis, migration ability, and invasiveness of COAD cells. RESULTS: In COAD cells, NEK6 was highly expressed, whereas miR-323a-3p was expressed at low levels and negatively regulated NEK6. Upregulating the level of miR-323a-3p impaired the proliferation, migration, and invasion of COAD cells and promoted apoptosis, whereas supplementing NEK6 alleviated the damage of the proliferation, migration, and invasion of COAD cells caused by miR-323a-3p and inhibited miR-323a-3p-induced apoptosis. These findings indicate that miR-323a-3p regulates the proliferation, migration, invasion, and apoptosis of COAD cells by targeting NEK6. CONCLUSION: miR-323a-3p downregulates NEK6 in COAD cells; this provides a novel basis for further understanding the occurrence and development of COAD. |
format | Online Article Text |
id | pubmed-8791743 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-87917432022-01-27 MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells Hong, Zhongshi Chen, Zhichuan Pan, Jianpeng Shi, Zesheng Wang, Chunxiao Qiu, Chengzhi J Oncol Research Article OBJECTIVE: The activity of NEK6 is enhanced in several cancer cells, including colon adenocarcinoma (COAD) cells. However, there are few reports on the microRNA (miRNA/miR) regulation of NEK6. In this study, we aimed to investigate the effects of miRNAs targeting NEK6 in COAD cells. METHODS: Public data and online analysis sites were used to analyze the expression levels of NEK6 and miR-323a-3p in COAD tissues as well as the relationship between NEK6 or miR-323a-3p levels and survival in patients with COAD and to predict miRNAs targeting NEK6. Real-time polymerase chain reaction and western blotting were performed to determine the levels of NEK6 and miR-323a-3p in COAD cells. The targeting of NEK6 by miR-323a-3p was verified using a dual-luciferase reporter assay. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, 5-ethynyl-2′-deoxyuridine assay, propidium iodide (PI) staining, annexin V-fluorescein isothiocyanate/PI staining, and transwell assay were employed to test the proliferation, apoptosis, migration ability, and invasiveness of COAD cells. RESULTS: In COAD cells, NEK6 was highly expressed, whereas miR-323a-3p was expressed at low levels and negatively regulated NEK6. Upregulating the level of miR-323a-3p impaired the proliferation, migration, and invasion of COAD cells and promoted apoptosis, whereas supplementing NEK6 alleviated the damage of the proliferation, migration, and invasion of COAD cells caused by miR-323a-3p and inhibited miR-323a-3p-induced apoptosis. These findings indicate that miR-323a-3p regulates the proliferation, migration, invasion, and apoptosis of COAD cells by targeting NEK6. CONCLUSION: miR-323a-3p downregulates NEK6 in COAD cells; this provides a novel basis for further understanding the occurrence and development of COAD. Hindawi 2022-01-19 /pmc/articles/PMC8791743/ /pubmed/35096064 http://dx.doi.org/10.1155/2022/7007718 Text en Copyright © 2022 Zhongshi Hong et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hong, Zhongshi Chen, Zhichuan Pan, Jianpeng Shi, Zesheng Wang, Chunxiao Qiu, Chengzhi MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells |
title | MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells |
title_full | MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells |
title_fullStr | MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells |
title_full_unstemmed | MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells |
title_short | MicroRNA-323a-3p Negatively Regulates NEK6 in Colon Adenocarcinoma Cells |
title_sort | microrna-323a-3p negatively regulates nek6 in colon adenocarcinoma cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791743/ https://www.ncbi.nlm.nih.gov/pubmed/35096064 http://dx.doi.org/10.1155/2022/7007718 |
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