MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells

MicroRNAs are critical regulators of gene networks in normal and abnormal biological processes. Focusing on invasive ductal breast cancer (IDC), we have found dysregulated expression in tumor samples of several microRNAs, including the miR-200 family, along progression from primary tumors to distant...

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Autores: Sánchez-Cid Pérez, Lourdes, Pons, Mònica, Lozano Salvatella, Juan José, Rubio, Nuria, Guerra-Rebollo, Marta, Soriano, Aroa, Paris-Coderch, Laia, Segura, Miguel F., Fueyo, Raquel, Arguimbau, Judit, Zodda, Erika, Bermudo, Raquel, Alonso Vargas, María Inmaculada, Caparrós, Xavier, Cascante i Serratosa, Marta, Rafii, Arash, Kang, Yibin, Martínez Balbás, Marian, Weiss, Stephen J., Blanco Fernández, Jerónimo, Muñoz, Montserrat, Fernández Ruiz, Pedro Luis, Thomsom, Timothy M.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/127217
Acceso en línea:https://hdl.handle.net/2445/127217
Access Level:acceso abierto
Palabra clave:Micro RNAs
Càncer de mama
Cèl·lules epitelials
MicroRNAs
Breast cancer
Epithelial cells
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repository_id_str
spelling MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cellsSánchez-Cid Pérez, LourdesPons, MònicaLozano Salvatella, Juan JoséRubio, NuriaGuerra-Rebollo, MartaSoriano, AroaParis-Coderch, LaiaSegura, Miguel F.Fueyo, RaquelArguimbau, JuditZodda, ErikaBermudo, RaquelAlonso Vargas, María InmaculadaCaparrós, XavierCascante i Serratosa, MartaRafii, ArashKang, YibinMartínez Balbás, MarianWeiss, Stephen J.Blanco Fernández, JerónimoMuñoz, MontserratFernández Ruiz, Pedro LuisThomsom, Timothy M.Micro RNAsCàncer de mamaCèl·lules epitelialsMicroRNAsBreast cancerEpithelial cellsMicroRNAs are critical regulators of gene networks in normal and abnormal biological processes. Focusing on invasive ductal breast cancer (IDC), we have found dysregulated expression in tumor samples of several microRNAs, including the miR-200 family, along progression from primary tumors to distant metastases, further reflected in higher blood levels of miR-200b and miR-7 in IDC patients with regional or distant metastases relative to patients with primary node-negative tumors. Forced expression of miR-200s in MCF10CA1h mammary cells induced an enhanced epithelial program, aldehyde dehydrogenase (ALDH) activity, mammosphere growth and ability to form branched tubuloalveolar structures while promoting orthotopic tumor growth and lung colonization in vivo. MiR-200s also induced the constitutive activation of the PI3K-Akt signaling through downregulation of PTEN, and the enhanced mammosphere growth and ALDH activity induced in MCF10CA1h cells by miR-200s required the activation of this signaling pathway. Interestingly, the morphology of tumors formed in vivo by cells expressing miR-200s was reminiscent of metaplastic breast cancer (MBC). Indeed, the epithelial components of MBC samples expressed significantly higher levels of miR-200s than their mesenchymal components and displayed a marker profile compatible with luminal progenitor cells. We propose that microRNAs of the miR-200 family promote traits of highly proliferative breast luminal progenitor cells, thereby exacerbating the growth and metastatic properties of transformed mammary epithelial cells.Impact Journals2019201920172019info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion23 p.application/pdfapplication/pdfhttps://hdl.handle.net/2445/127217Articles publicats en revistes (Bioquímica i Biomedicina Molecular)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.18632/oncotarget.20698Oncotarget, 2017, vol. 8, num. 48https://doi.org/10.18632/oncotarget.20698cc-by (c) Sánchez-Cid Pérez, Lourdes et al., 2017http://creativecommons.org/licenses/by/3.0/esinfo:eu-repo/semantics/openAccessoai:recercat.cat:2445/1272172026-05-29T05:05:01Z
dc.title.none.fl_str_mv MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
title MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
spellingShingle MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
Sánchez-Cid Pérez, Lourdes
Micro RNAs
Càncer de mama
Cèl·lules epitelials
MicroRNAs
Breast cancer
Epithelial cells
title_short MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
title_full MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
title_fullStr MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
title_full_unstemmed MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
title_sort MicroRNA-200, associated with metastatic breast cancer, promotes traits of mammary luminal progenitor cells
dc.creator.none.fl_str_mv Sánchez-Cid Pérez, Lourdes
Pons, Mònica
Lozano Salvatella, Juan José
Rubio, Nuria
Guerra-Rebollo, Marta
Soriano, Aroa
Paris-Coderch, Laia
Segura, Miguel F.
Fueyo, Raquel
Arguimbau, Judit
Zodda, Erika
Bermudo, Raquel
Alonso Vargas, María Inmaculada
Caparrós, Xavier
Cascante i Serratosa, Marta
Rafii, Arash
Kang, Yibin
Martínez Balbás, Marian
Weiss, Stephen J.
Blanco Fernández, Jerónimo
Muñoz, Montserrat
Fernández Ruiz, Pedro Luis
Thomsom, Timothy M.
author Sánchez-Cid Pérez, Lourdes
author_facet Sánchez-Cid Pérez, Lourdes
Pons, Mònica
Lozano Salvatella, Juan José
Rubio, Nuria
Guerra-Rebollo, Marta
Soriano, Aroa
Paris-Coderch, Laia
Segura, Miguel F.
Fueyo, Raquel
Arguimbau, Judit
Zodda, Erika
Bermudo, Raquel
Alonso Vargas, María Inmaculada
Caparrós, Xavier
Cascante i Serratosa, Marta
Rafii, Arash
Kang, Yibin
Martínez Balbás, Marian
Weiss, Stephen J.
Blanco Fernández, Jerónimo
Muñoz, Montserrat
Fernández Ruiz, Pedro Luis
Thomsom, Timothy M.
author_role author
author2 Pons, Mònica
Lozano Salvatella, Juan José
Rubio, Nuria
Guerra-Rebollo, Marta
Soriano, Aroa
Paris-Coderch, Laia
Segura, Miguel F.
Fueyo, Raquel
Arguimbau, Judit
Zodda, Erika
Bermudo, Raquel
Alonso Vargas, María Inmaculada
Caparrós, Xavier
Cascante i Serratosa, Marta
Rafii, Arash
Kang, Yibin
Martínez Balbás, Marian
Weiss, Stephen J.
Blanco Fernández, Jerónimo
Muñoz, Montserrat
Fernández Ruiz, Pedro Luis
Thomsom, Timothy M.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Micro RNAs
Càncer de mama
Cèl·lules epitelials
MicroRNAs
Breast cancer
Epithelial cells
topic Micro RNAs
Càncer de mama
Cèl·lules epitelials
MicroRNAs
Breast cancer
Epithelial cells
description MicroRNAs are critical regulators of gene networks in normal and abnormal biological processes. Focusing on invasive ductal breast cancer (IDC), we have found dysregulated expression in tumor samples of several microRNAs, including the miR-200 family, along progression from primary tumors to distant metastases, further reflected in higher blood levels of miR-200b and miR-7 in IDC patients with regional or distant metastases relative to patients with primary node-negative tumors. Forced expression of miR-200s in MCF10CA1h mammary cells induced an enhanced epithelial program, aldehyde dehydrogenase (ALDH) activity, mammosphere growth and ability to form branched tubuloalveolar structures while promoting orthotopic tumor growth and lung colonization in vivo. MiR-200s also induced the constitutive activation of the PI3K-Akt signaling through downregulation of PTEN, and the enhanced mammosphere growth and ALDH activity induced in MCF10CA1h cells by miR-200s required the activation of this signaling pathway. Interestingly, the morphology of tumors formed in vivo by cells expressing miR-200s was reminiscent of metaplastic breast cancer (MBC). Indeed, the epithelial components of MBC samples expressed significantly higher levels of miR-200s than their mesenchymal components and displayed a marker profile compatible with luminal progenitor cells. We propose that microRNAs of the miR-200 family promote traits of highly proliferative breast luminal progenitor cells, thereby exacerbating the growth and metastatic properties of transformed mammary epithelial cells.
publishDate 2017
dc.date.none.fl_str_mv 2017
2019
2019
2019
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/2445/127217
url https://hdl.handle.net/2445/127217
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Reproducció del document publicat a: https://doi.org/10.18632/oncotarget.20698
Oncotarget, 2017, vol. 8, num. 48
https://doi.org/10.18632/oncotarget.20698
dc.rights.none.fl_str_mv cc-by (c) Sánchez-Cid Pérez, Lourdes et al., 2017
http://creativecommons.org/licenses/by/3.0/es
info:eu-repo/semantics/openAccess
rights_invalid_str_mv cc-by (c) Sánchez-Cid Pérez, Lourdes et al., 2017
http://creativecommons.org/licenses/by/3.0/es
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 23 p.
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Impact Journals
publisher.none.fl_str_mv Impact Journals
dc.source.none.fl_str_mv Articles publicats en revistes (Bioquímica i Biomedicina Molecular)
reponame:Recercat. Dipósit de la Recerca de Catalunya
instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
reponame_str Recercat. Dipósit de la Recerca de Catalunya
collection Recercat. Dipósit de la Recerca de Catalunya
repository.name.fl_str_mv
repository.mail.fl_str_mv
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