The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration

Detalhes bibliográficos
Autor(a) principal: Silveira, Marina Bonfogo da [UNESP]
Data de Publicação: 2021
Outros Autores: Pansa, Camila Cristiane [UNESP], Malaspina, Osmar [UNESP], Moraes, Karen C. M. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s11033-021-06364-3
http://hdl.handle.net/11449/210278
Resumo: Hepatocellular carcinoma is one of the most common types of cancer in the world with high mortality rate and new therapies that control of fatty acid metabolism may limit the proliferation of cancer cells. In the last two decades, the non-coding RNAs have been considered as promising molecular tools to treat diseases, because they are able to modulate gene expression and the metabolic routes; however, deep investigation of their mechanistic behavior in pathologies must be performed. Thus, our aim was to evaluate the modulatory effect of the miR-1914-5p in controlling lipid metabolism in HepG2, a widely used human hepatocarcinoma cell line. The molecular and cellular analyses demonstrated that the functional inhibition of the investigated microRNA completely changed the cellular metabolism and behavior, compared to control groups. The in vitro inhibition of the miR-1914-5p increased the energy expenditure pointed in different analyses, decreasing cell doubling time and migration rate verified in wound healing and in the classical transwell chambers invasion assays, which makes the miR-1914-5p a candidate for further translational and preclinical studies to validate its function in controlling metastasis in liver cancer or even treat those diseases.
id UNSP_b8dd91427c10a75368b19a7585f092f4
oai_identifier_str oai:repositorio.unesp.br:11449/210278
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migrationCell migrationCellular mechanismsHepatic diseaseLipid metabolismNon-coding RNAsSystems biologyHepatocellular carcinoma is one of the most common types of cancer in the world with high mortality rate and new therapies that control of fatty acid metabolism may limit the proliferation of cancer cells. In the last two decades, the non-coding RNAs have been considered as promising molecular tools to treat diseases, because they are able to modulate gene expression and the metabolic routes; however, deep investigation of their mechanistic behavior in pathologies must be performed. Thus, our aim was to evaluate the modulatory effect of the miR-1914-5p in controlling lipid metabolism in HepG2, a widely used human hepatocarcinoma cell line. The molecular and cellular analyses demonstrated that the functional inhibition of the investigated microRNA completely changed the cellular metabolism and behavior, compared to control groups. The in vitro inhibition of the miR-1914-5p increased the energy expenditure pointed in different analyses, decreasing cell doubling time and migration rate verified in wound healing and in the classical transwell chambers invasion assays, which makes the miR-1914-5p a candidate for further translational and preclinical studies to validate its function in controlling metastasis in liver cancer or even treat those diseases.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Estadual Paulista, Dept Biol Geral & Aplicada, Inst Biociencias, Lab Biol Mol, Campus Rio Claro, BR-13506900 Rio Claro, SP, BrazilUniv Estadual Paulista, Ctr Estudos Insetos Sociais, Inst Biociencia, Rio Claro, SP, BrazilUniv Estadual Paulista, Dept Biol Geral & Aplicada, Inst Biociencias, Lab Biol Mol, Campus Rio Claro, BR-13506900 Rio Claro, SP, BrazilUniv Estadual Paulista, Ctr Estudos Insetos Sociais, Inst Biociencia, Rio Claro, SP, BrazilFAPESP: FAPESP-2013/21186-5FAPESP: 2018/05286-3SpringerUniversidade Estadual Paulista (Unesp)Silveira, Marina Bonfogo da [UNESP]Pansa, Camila Cristiane [UNESP]Malaspina, Osmar [UNESP]Moraes, Karen C. M. [UNESP]2021-06-25T15:03:31Z2021-06-25T15:03:31Z2021-04-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article12http://dx.doi.org/10.1007/s11033-021-06364-3Molecular Biology Reports. Dordrecht: Springer, 12 p., 2021.0301-4851http://hdl.handle.net/11449/21027810.1007/s11033-021-06364-3WOS:000644750500001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMolecular Biology Reportsinfo:eu-repo/semantics/openAccess2021-10-23T20:17:26Zoai:repositorio.unesp.br:11449/210278Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:09:19.475386Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
title The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
spellingShingle The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
Silveira, Marina Bonfogo da [UNESP]
Cell migration
Cellular mechanisms
Hepatic disease
Lipid metabolism
Non-coding RNAs
Systems biology
title_short The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
title_full The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
title_fullStr The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
title_full_unstemmed The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
title_sort The functional activity of the miR-1914-5p in lipid metabolism of the hepatocarcinoma cell line HepG2: a potential molecular tool for controlling hepatic cellular migration
author Silveira, Marina Bonfogo da [UNESP]
author_facet Silveira, Marina Bonfogo da [UNESP]
Pansa, Camila Cristiane [UNESP]
Malaspina, Osmar [UNESP]
Moraes, Karen C. M. [UNESP]
author_role author
author2 Pansa, Camila Cristiane [UNESP]
Malaspina, Osmar [UNESP]
Moraes, Karen C. M. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Silveira, Marina Bonfogo da [UNESP]
Pansa, Camila Cristiane [UNESP]
Malaspina, Osmar [UNESP]
Moraes, Karen C. M. [UNESP]
dc.subject.por.fl_str_mv Cell migration
Cellular mechanisms
Hepatic disease
Lipid metabolism
Non-coding RNAs
Systems biology
topic Cell migration
Cellular mechanisms
Hepatic disease
Lipid metabolism
Non-coding RNAs
Systems biology
description Hepatocellular carcinoma is one of the most common types of cancer in the world with high mortality rate and new therapies that control of fatty acid metabolism may limit the proliferation of cancer cells. In the last two decades, the non-coding RNAs have been considered as promising molecular tools to treat diseases, because they are able to modulate gene expression and the metabolic routes; however, deep investigation of their mechanistic behavior in pathologies must be performed. Thus, our aim was to evaluate the modulatory effect of the miR-1914-5p in controlling lipid metabolism in HepG2, a widely used human hepatocarcinoma cell line. The molecular and cellular analyses demonstrated that the functional inhibition of the investigated microRNA completely changed the cellular metabolism and behavior, compared to control groups. The in vitro inhibition of the miR-1914-5p increased the energy expenditure pointed in different analyses, decreasing cell doubling time and migration rate verified in wound healing and in the classical transwell chambers invasion assays, which makes the miR-1914-5p a candidate for further translational and preclinical studies to validate its function in controlling metastasis in liver cancer or even treat those diseases.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T15:03:31Z
2021-06-25T15:03:31Z
2021-04-28
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s11033-021-06364-3
Molecular Biology Reports. Dordrecht: Springer, 12 p., 2021.
0301-4851
http://hdl.handle.net/11449/210278
10.1007/s11033-021-06364-3
WOS:000644750500001
url http://dx.doi.org/10.1007/s11033-021-06364-3
http://hdl.handle.net/11449/210278
identifier_str_mv Molecular Biology Reports. Dordrecht: Springer, 12 p., 2021.
0301-4851
10.1007/s11033-021-06364-3
WOS:000644750500001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Molecular Biology Reports
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 12
dc.publisher.none.fl_str_mv Springer
publisher.none.fl_str_mv Springer
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808128323199434752