MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib

Detalhes bibliográficos
Autor(a) principal: Bordinhão, A. L. R.
Data de Publicação: 2016
Outros Autores: Evangelista, Adriane F., Oliveira, R. J. S., Macedo, Taciane, Silveira, Henrique C. S., Reis, R. M., Marques, Marcia M. C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/45040
Resumo: Cediranib, a pan-tyrosine kinase inhibitor is showing promising results for the treatment of several solid tumours. In breast cancer, its effects remain unclear, and there are no predictive biomarkers. Several studies have examined the expression profiles of microRNAs (miRNAs) in response to different chemotherapy treatments and found that the expression patterns may be associated with the treatment response. Therefore, our aim was to evaluate the cellular behaviour and differential expression profiles of miRNAs in breast cancer cell lines exposed to cediranib. The biological effect of this drug was measured by viability, migration, invasion and cell death in in vitro assays. Signaling pathways were assessed using a human phospho-receptor tyrosine kinase array. Furthermore, using a miRNA array and quantitative real-time PCR (qRT-PCR), we assessed the relative expression of miRNAs following cediranib treatment. The breast cancer cell lines exhibited a distinct cytotoxic response to cediranib treatment. Cediranib exposure resulted in a decrease in the cell migration and invasion of all the breast cancer cell lines. Treatment with cediranib appeared to be able to modulate the activation of several RTKs that are targets of cediranib such as EGFR and a new potential target ROR2. Furthermore, this drug was able to modulate the expression profile of different microRNAs such as miR-494, miR-923, miR-449a, miR-449b and miR-886-3 in breast cancer cell lines. These miRNAs are reported to regulate genes involved in important molecular processes, according to bioinformatics prediction tools.
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spelling MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranibBreast cancer cell linesXediranibCellular behaviourMicroRNA expressionMicroarrayscediranibScience & TechnologyCediranib, a pan-tyrosine kinase inhibitor is showing promising results for the treatment of several solid tumours. In breast cancer, its effects remain unclear, and there are no predictive biomarkers. Several studies have examined the expression profiles of microRNAs (miRNAs) in response to different chemotherapy treatments and found that the expression patterns may be associated with the treatment response. Therefore, our aim was to evaluate the cellular behaviour and differential expression profiles of miRNAs in breast cancer cell lines exposed to cediranib. The biological effect of this drug was measured by viability, migration, invasion and cell death in in vitro assays. Signaling pathways were assessed using a human phospho-receptor tyrosine kinase array. Furthermore, using a miRNA array and quantitative real-time PCR (qRT-PCR), we assessed the relative expression of miRNAs following cediranib treatment. The breast cancer cell lines exhibited a distinct cytotoxic response to cediranib treatment. Cediranib exposure resulted in a decrease in the cell migration and invasion of all the breast cancer cell lines. Treatment with cediranib appeared to be able to modulate the activation of several RTKs that are targets of cediranib such as EGFR and a new potential target ROR2. Furthermore, this drug was able to modulate the expression profile of different microRNAs such as miR-494, miR-923, miR-449a, miR-449b and miR-886-3 in breast cancer cell lines. These miRNAs are reported to regulate genes involved in important molecular processes, according to bioinformatics prediction tools.We would like to thank Olga Martinho and Celine Pinheiro for assisting in the cellular experiments. This study received financial support from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP Proc. no. 2010/16796-0, São Paulo, brazil).Spandidos PublicationsUniversidade do MinhoBordinhão, A. L. R.Evangelista, Adriane F.Oliveira, R. J. S.Macedo, TacianeSilveira, Henrique C. S.Reis, R. M.Marques, Marcia M. C.20162016-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/45040engBordinhao, A. L. R., Evangelist, A. F., Oliveira, R. J. S., MacEdo, T., Silveir, H. C., Rei, R. M., & Marques, M. M. (2016). MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib. Oncology Reports, 36(6), 3197-3206. doi: 10.3892/or.2016.51531021-335X1791-243110.3892/or.2016.515327748845https://www.spandidos-publications.com/or/36/6/3197info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:52:29Zoai:repositorium.sdum.uminho.pt:1822/45040Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:51:37.851634Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
title MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
spellingShingle MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
Bordinhão, A. L. R.
Breast cancer cell lines
Xediranib
Cellular behaviour
MicroRNA expression
Microarrays
cediranib
Science & Technology
title_short MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
title_full MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
title_fullStr MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
title_full_unstemmed MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
title_sort MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib
author Bordinhão, A. L. R.
author_facet Bordinhão, A. L. R.
Evangelista, Adriane F.
Oliveira, R. J. S.
Macedo, Taciane
Silveira, Henrique C. S.
Reis, R. M.
Marques, Marcia M. C.
author_role author
author2 Evangelista, Adriane F.
Oliveira, R. J. S.
Macedo, Taciane
Silveira, Henrique C. S.
Reis, R. M.
Marques, Marcia M. C.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Bordinhão, A. L. R.
Evangelista, Adriane F.
Oliveira, R. J. S.
Macedo, Taciane
Silveira, Henrique C. S.
Reis, R. M.
Marques, Marcia M. C.
dc.subject.por.fl_str_mv Breast cancer cell lines
Xediranib
Cellular behaviour
MicroRNA expression
Microarrays
cediranib
Science & Technology
topic Breast cancer cell lines
Xediranib
Cellular behaviour
MicroRNA expression
Microarrays
cediranib
Science & Technology
description Cediranib, a pan-tyrosine kinase inhibitor is showing promising results for the treatment of several solid tumours. In breast cancer, its effects remain unclear, and there are no predictive biomarkers. Several studies have examined the expression profiles of microRNAs (miRNAs) in response to different chemotherapy treatments and found that the expression patterns may be associated with the treatment response. Therefore, our aim was to evaluate the cellular behaviour and differential expression profiles of miRNAs in breast cancer cell lines exposed to cediranib. The biological effect of this drug was measured by viability, migration, invasion and cell death in in vitro assays. Signaling pathways were assessed using a human phospho-receptor tyrosine kinase array. Furthermore, using a miRNA array and quantitative real-time PCR (qRT-PCR), we assessed the relative expression of miRNAs following cediranib treatment. The breast cancer cell lines exhibited a distinct cytotoxic response to cediranib treatment. Cediranib exposure resulted in a decrease in the cell migration and invasion of all the breast cancer cell lines. Treatment with cediranib appeared to be able to modulate the activation of several RTKs that are targets of cediranib such as EGFR and a new potential target ROR2. Furthermore, this drug was able to modulate the expression profile of different microRNAs such as miR-494, miR-923, miR-449a, miR-449b and miR-886-3 in breast cancer cell lines. These miRNAs are reported to regulate genes involved in important molecular processes, according to bioinformatics prediction tools.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-01-01T00:00:00Z
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://hdl.handle.net/1822/45040
url http://hdl.handle.net/1822/45040
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Bordinhao, A. L. R., Evangelist, A. F., Oliveira, R. J. S., MacEdo, T., Silveir, H. C., Rei, R. M., & Marques, M. M. (2016). MicroRNA profiling in human breast cancer cell lines exposed to the anti-neoplastic drug cediranib. Oncology Reports, 36(6), 3197-3206. doi: 10.3892/or.2016.5153
1021-335X
1791-2431
10.3892/or.2016.5153
27748845
https://www.spandidos-publications.com/or/36/6/3197
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Spandidos Publications
publisher.none.fl_str_mv Spandidos Publications
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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