miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma

Detalhes bibliográficos
Autor(a) principal: Lopes, Beatriz C. [UNESP]
Data de Publicação: 2021
Outros Autores: Braga, Cristine Z., Ventura, Fabricio V., Oliveira, Jessica G. de, Kato-Junior, Edson M., Bordin-Junior, Newton A., Zuccari, Debora A. P. C. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.3390/jpm11010031
http://hdl.handle.net/11449/209128
Resumo: Detecting circulating microRNAs (miRNAs; miRs) by means of liquid biopsy is an important tool for the early diagnosis and prognosis of breast cancer (BC). We aimed to identify and validate miR-210 and miR-152 as non-invasive circulating biomarkers, for the diagnosis and staging of BC patients, confirming their involvement in tumor angiogenesis. Methods: RT-qPCR was performed and MiRNA expression analysis was obtained from plasma and fragments of BC and benign breast condition (BBC) women patients, plus healthy subjects. Additionally, the immunohistochemistry technique was carried out to analyze the expression of target proteins. Results: Tumor fragments showed increased expression of oncomiR-210 and decreased expression of miR-152 tumoral suppressor. Both miRNAs were increased in plasma samples from BC patients. The receiver operating characteristic (ROC) curve analysis revealed that only the expression of oncomiR-210 in tissue samples and only the expression of the miR-152 suppressor in plasma have the appropriate sensitivity and specificity for use as differential biomarkers between early/intermediate and advanced stages of BC patients. In addition, there was an increase in the expression of hypoxia-inducible factor 1-alpha (HIF-1 alpha), insulin-like growth factor 1 receptor (IGF-1R), and vascular endothelial growth factor (VEGF) in BC patients. On the contrary, a decrease in Von Hippel-Lindau (VHL) protein expression was observed. Conclusions: This study showed that increased levels of miR-210 and decreased levels of miR152, in addition to the expressions of their target proteins, could indicate, respectively, the oncogenic and tumor suppressive role of these miRNAs in fragments. Both miRNAs are potential diagnostic biomarkers for BC by liquid biopsy. In addition, miR-152 proved to be a promising biomarker for disease staging.
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spelling miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinomabreast cancermiRNAsliquid biopsyangiogenesisbiomarkersearly diagnosisDetecting circulating microRNAs (miRNAs; miRs) by means of liquid biopsy is an important tool for the early diagnosis and prognosis of breast cancer (BC). We aimed to identify and validate miR-210 and miR-152 as non-invasive circulating biomarkers, for the diagnosis and staging of BC patients, confirming their involvement in tumor angiogenesis. Methods: RT-qPCR was performed and MiRNA expression analysis was obtained from plasma and fragments of BC and benign breast condition (BBC) women patients, plus healthy subjects. Additionally, the immunohistochemistry technique was carried out to analyze the expression of target proteins. Results: Tumor fragments showed increased expression of oncomiR-210 and decreased expression of miR-152 tumoral suppressor. Both miRNAs were increased in plasma samples from BC patients. The receiver operating characteristic (ROC) curve analysis revealed that only the expression of oncomiR-210 in tissue samples and only the expression of the miR-152 suppressor in plasma have the appropriate sensitivity and specificity for use as differential biomarkers between early/intermediate and advanced stages of BC patients. In addition, there was an increase in the expression of hypoxia-inducible factor 1-alpha (HIF-1 alpha), insulin-like growth factor 1 receptor (IGF-1R), and vascular endothelial growth factor (VEGF) in BC patients. On the contrary, a decrease in Von Hippel-Lindau (VHL) protein expression was observed. Conclusions: This study showed that increased levels of miR-210 and decreased levels of miR152, in addition to the expressions of their target proteins, could indicate, respectively, the oncogenic and tumor suppressive role of these miRNAs in fragments. Both miRNAs are potential diagnostic biomarkers for BC by liquid biopsy. In addition, miR-152 proved to be a promising biomarker for disease staging.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fundacao de Apoio a Pesquisa e Extensao de Sao Jose do Rio Preto (FAPERP)Inst Biosci Letters & Exact Sci IBILCE, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilFac Med Sao Jose do Rio Preto FAMERP, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilHosp Base Sao Jose do Rio Preto, BR-15090000 Sao Jose Do Rio Preto, SP, BrazilLab Mol Invest Canc LIMC, Ave Brigadeiro Faria Lima 5416, BR-15090000 Sao Jose Do Rio Preto, SP, BrazilInst Biosci Letters & Exact Sci IBILCE, BR-15054000 Sao Jose Do Rio Preto, SP, BrazilFAPESP: 2017/11807-3FAPESP: 2017/15006-5Fundacao de Apoio a Pesquisa e Extensao de Sao Jose do Rio Preto (FAPERP): 028/2018MdpiUniversidade Estadual Paulista (Unesp)Fac Med Sao Jose do Rio Preto FAMERPHosp Base Sao Jose do Rio PretoLab Mol Invest Canc LIMCLopes, Beatriz C. [UNESP]Braga, Cristine Z.Ventura, Fabricio V.Oliveira, Jessica G. deKato-Junior, Edson M.Bordin-Junior, Newton A.Zuccari, Debora A. P. C. [UNESP]2021-06-25T11:49:22Z2021-06-25T11:49:22Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article17http://dx.doi.org/10.3390/jpm11010031Journal Of Personalized Medicine. Basel: Mdpi, v. 11, n. 1, 17 p., 2021.http://hdl.handle.net/11449/20912810.3390/jpm11010031WOS:000610348300001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Personalized Medicineinfo:eu-repo/semantics/openAccess2021-10-23T19:23:33Zoai:repositorio.unesp.br:11449/209128Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:31:58.180317Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
title miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
spellingShingle miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
Lopes, Beatriz C. [UNESP]
breast cancer
miRNAs
liquid biopsy
angiogenesis
biomarkers
early diagnosis
title_short miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
title_full miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
title_fullStr miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
title_full_unstemmed miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
title_sort miR-210 and miR-152 as Biomarkers by Liquid Biopsy in Invasive Ductal Carcinoma
author Lopes, Beatriz C. [UNESP]
author_facet Lopes, Beatriz C. [UNESP]
Braga, Cristine Z.
Ventura, Fabricio V.
Oliveira, Jessica G. de
Kato-Junior, Edson M.
Bordin-Junior, Newton A.
Zuccari, Debora A. P. C. [UNESP]
author_role author
author2 Braga, Cristine Z.
Ventura, Fabricio V.
Oliveira, Jessica G. de
Kato-Junior, Edson M.
Bordin-Junior, Newton A.
Zuccari, Debora A. P. C. [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Fac Med Sao Jose do Rio Preto FAMERP
Hosp Base Sao Jose do Rio Preto
Lab Mol Invest Canc LIMC
dc.contributor.author.fl_str_mv Lopes, Beatriz C. [UNESP]
Braga, Cristine Z.
Ventura, Fabricio V.
Oliveira, Jessica G. de
Kato-Junior, Edson M.
Bordin-Junior, Newton A.
Zuccari, Debora A. P. C. [UNESP]
dc.subject.por.fl_str_mv breast cancer
miRNAs
liquid biopsy
angiogenesis
biomarkers
early diagnosis
topic breast cancer
miRNAs
liquid biopsy
angiogenesis
biomarkers
early diagnosis
description Detecting circulating microRNAs (miRNAs; miRs) by means of liquid biopsy is an important tool for the early diagnosis and prognosis of breast cancer (BC). We aimed to identify and validate miR-210 and miR-152 as non-invasive circulating biomarkers, for the diagnosis and staging of BC patients, confirming their involvement in tumor angiogenesis. Methods: RT-qPCR was performed and MiRNA expression analysis was obtained from plasma and fragments of BC and benign breast condition (BBC) women patients, plus healthy subjects. Additionally, the immunohistochemistry technique was carried out to analyze the expression of target proteins. Results: Tumor fragments showed increased expression of oncomiR-210 and decreased expression of miR-152 tumoral suppressor. Both miRNAs were increased in plasma samples from BC patients. The receiver operating characteristic (ROC) curve analysis revealed that only the expression of oncomiR-210 in tissue samples and only the expression of the miR-152 suppressor in plasma have the appropriate sensitivity and specificity for use as differential biomarkers between early/intermediate and advanced stages of BC patients. In addition, there was an increase in the expression of hypoxia-inducible factor 1-alpha (HIF-1 alpha), insulin-like growth factor 1 receptor (IGF-1R), and vascular endothelial growth factor (VEGF) in BC patients. On the contrary, a decrease in Von Hippel-Lindau (VHL) protein expression was observed. Conclusions: This study showed that increased levels of miR-210 and decreased levels of miR152, in addition to the expressions of their target proteins, could indicate, respectively, the oncogenic and tumor suppressive role of these miRNAs in fragments. Both miRNAs are potential diagnostic biomarkers for BC by liquid biopsy. In addition, miR-152 proved to be a promising biomarker for disease staging.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T11:49:22Z
2021-06-25T11:49:22Z
2021-01-01
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/10.3390/jpm11010031
Journal Of Personalized Medicine. Basel: Mdpi, v. 11, n. 1, 17 p., 2021.
http://hdl.handle.net/11449/209128
10.3390/jpm11010031
WOS:000610348300001
url http://dx.doi.org/10.3390/jpm11010031
http://hdl.handle.net/11449/209128
identifier_str_mv Journal Of Personalized Medicine. Basel: Mdpi, v. 11, n. 1, 17 p., 2021.
10.3390/jpm11010031
WOS:000610348300001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Personalized Medicine
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 17
dc.publisher.none.fl_str_mv Mdpi
publisher.none.fl_str_mv Mdpi
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
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