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MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55

This study evaluated microRNA-148a-3p in esophageal carcinoma cells. The prediction of bioinformatics analysis revealed that microRNA-148a-3p may target CEP55. qRT-PCR and western blot showed that CEP55 level in esophageal carcinoma cells and tissue was dramatically higher than that of normal cells...

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Autores principales: Lin, Yong, Chen, Yushan, Shen, Rongqiang, Chen, Dingzhu, Lin, Yimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903601/
https://www.ncbi.nlm.nih.gov/pubmed/34952571
http://dx.doi.org/10.1186/s11658-021-00298-1
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author Lin, Yong
Chen, Yushan
Shen, Rongqiang
Chen, Dingzhu
Lin, Yimin
author_facet Lin, Yong
Chen, Yushan
Shen, Rongqiang
Chen, Dingzhu
Lin, Yimin
author_sort Lin, Yong
collection PubMed
description This study evaluated microRNA-148a-3p in esophageal carcinoma cells. The prediction of bioinformatics analysis revealed that microRNA-148a-3p may target CEP55. qRT-PCR and western blot showed that CEP55 level in esophageal carcinoma cells and tissue was dramatically higher than that of normal cells and tissue, while microRNA-148a-3p was the opposite. Forced expression of microRNA-148a-3p restrained cell malignant behaviors of esophageal carcinoma, and repression of microRNA-148a-3p resulted in the converse results in terms of cell function. Dual-luciferase assay confirmed that microRNA-148a-3p targeted CEP55. CEP55 attenuated the suppressive effect of microRNA-148a-3p on proliferation and migration of esophageal carcinoma cells, demonstrating that microRNA-148a-3p regulated function of esophageal carcinoma cells via decreasing CEP55 level. Microscopy observation indicated that cell morphology was also affected by the microRNA-148a-3p/CEP55 axis. Furthermore, western blot analysis revealed that the PI3K/AKT signaling pathway could be suppressed by activating the microRNA-148a-3p/CEP55 axis. Finally, in vivo experiments confirmed the effects of microRNA-148a-3p on tumorigenesis. Thus, microRNA-148a-3p could act as a repressor in esophageal carcinoma via binding to CEP55. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11658-021-00298-1.
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spelling pubmed-89036012022-03-23 MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55 Lin, Yong Chen, Yushan Shen, Rongqiang Chen, Dingzhu Lin, Yimin Cell Mol Biol Lett Research Letter This study evaluated microRNA-148a-3p in esophageal carcinoma cells. The prediction of bioinformatics analysis revealed that microRNA-148a-3p may target CEP55. qRT-PCR and western blot showed that CEP55 level in esophageal carcinoma cells and tissue was dramatically higher than that of normal cells and tissue, while microRNA-148a-3p was the opposite. Forced expression of microRNA-148a-3p restrained cell malignant behaviors of esophageal carcinoma, and repression of microRNA-148a-3p resulted in the converse results in terms of cell function. Dual-luciferase assay confirmed that microRNA-148a-3p targeted CEP55. CEP55 attenuated the suppressive effect of microRNA-148a-3p on proliferation and migration of esophageal carcinoma cells, demonstrating that microRNA-148a-3p regulated function of esophageal carcinoma cells via decreasing CEP55 level. Microscopy observation indicated that cell morphology was also affected by the microRNA-148a-3p/CEP55 axis. Furthermore, western blot analysis revealed that the PI3K/AKT signaling pathway could be suppressed by activating the microRNA-148a-3p/CEP55 axis. Finally, in vivo experiments confirmed the effects of microRNA-148a-3p on tumorigenesis. Thus, microRNA-148a-3p could act as a repressor in esophageal carcinoma via binding to CEP55. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s11658-021-00298-1. BioMed Central 2021-12-24 /pmc/articles/PMC8903601/ /pubmed/34952571 http://dx.doi.org/10.1186/s11658-021-00298-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) .
spellingShingle Research Letter
Lin, Yong
Chen, Yushan
Shen, Rongqiang
Chen, Dingzhu
Lin, Yimin
MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55
title MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55
title_full MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55
title_fullStr MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55
title_full_unstemmed MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55
title_short MicroRNA-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting CEP55
title_sort microrna-148a-3p suppresses cell proliferation and migration of esophageal carcinoma by targeting cep55
topic Research Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903601/
https://www.ncbi.nlm.nih.gov/pubmed/34952571
http://dx.doi.org/10.1186/s11658-021-00298-1
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