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Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression

Cancer stem cells (CSC) exhibit high tumorigenic capacity in several tumor models. We have now determined an extended phenotype for cervical cancer stem cells. Our results showed increased CK-17, p63(+), AII(+), CD49f(+) expression in these cells, together with higher Aldehyde dehydrogenase (ALDH(br...

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Autores principales: Ortiz-Sánchez, Elizabeth, Santiago-López, Luz, Cruz-Domínguez, Verónica B., Toledo-Guzmán, Mariel E., Hernández-Cueto, Daniel, Muñiz-Hernández, Saé, Garrido, Efraín, De León, David Cantú, García-Carrancá, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077987/
https://www.ncbi.nlm.nih.gov/pubmed/27008711
http://dx.doi.org/10.18632/oncotarget.8218
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author Ortiz-Sánchez, Elizabeth
Santiago-López, Luz
Cruz-Domínguez, Verónica B.
Toledo-Guzmán, Mariel E.
Hernández-Cueto, Daniel
Muñiz-Hernández, Saé
Garrido, Efraín
De León, David Cantú
García-Carrancá, Alejandro
author_facet Ortiz-Sánchez, Elizabeth
Santiago-López, Luz
Cruz-Domínguez, Verónica B.
Toledo-Guzmán, Mariel E.
Hernández-Cueto, Daniel
Muñiz-Hernández, Saé
Garrido, Efraín
De León, David Cantú
García-Carrancá, Alejandro
author_sort Ortiz-Sánchez, Elizabeth
collection PubMed
description Cancer stem cells (CSC) exhibit high tumorigenic capacity in several tumor models. We have now determined an extended phenotype for cervical cancer stem cells. Our results showed increased CK-17, p63(+), AII(+), CD49f(+) expression in these cells, together with higher Aldehyde dehydrogenase (ALDH(bright))activity in Cervical CSC (CCSC) enriched in cervospheres. An increase in stem cell markers, represented by OCT-4, Nanog, and β-catenin proteins, was also observed, indicating that under our culture conditions, CCSC are enriched in cervospheres, as compared to monolayer cultures. In addition, we were able to show that an increased ALDH(bright) activity correlated with higher tumorigenic activity. Flow cytometry and immunflorescence assays demonstrated that CCSC in cervosphere cultures contain a sub-population of cells that contain Annexin II, a Human papillomavirus (HPV) co-receptor. Taken together, under our conditions there is an increase in the number of CCSC in cervosphere cultures which exhibit the following phenotype: CK-17, p63(+), AII(+), CD49f(+) and high ALDH activity, which in turn correlates with higher tumorigenicity. The presence of Annexin II and CD49f in CCSC opens the possibility that normal cervical stem cells could be the initial target of infection by high risk HPV.
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spelling pubmed-50779872016-10-28 Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression Ortiz-Sánchez, Elizabeth Santiago-López, Luz Cruz-Domínguez, Verónica B. Toledo-Guzmán, Mariel E. Hernández-Cueto, Daniel Muñiz-Hernández, Saé Garrido, Efraín De León, David Cantú García-Carrancá, Alejandro Oncotarget Research Paper Cancer stem cells (CSC) exhibit high tumorigenic capacity in several tumor models. We have now determined an extended phenotype for cervical cancer stem cells. Our results showed increased CK-17, p63(+), AII(+), CD49f(+) expression in these cells, together with higher Aldehyde dehydrogenase (ALDH(bright))activity in Cervical CSC (CCSC) enriched in cervospheres. An increase in stem cell markers, represented by OCT-4, Nanog, and β-catenin proteins, was also observed, indicating that under our culture conditions, CCSC are enriched in cervospheres, as compared to monolayer cultures. In addition, we were able to show that an increased ALDH(bright) activity correlated with higher tumorigenic activity. Flow cytometry and immunflorescence assays demonstrated that CCSC in cervosphere cultures contain a sub-population of cells that contain Annexin II, a Human papillomavirus (HPV) co-receptor. Taken together, under our conditions there is an increase in the number of CCSC in cervosphere cultures which exhibit the following phenotype: CK-17, p63(+), AII(+), CD49f(+) and high ALDH activity, which in turn correlates with higher tumorigenicity. The presence of Annexin II and CD49f in CCSC opens the possibility that normal cervical stem cells could be the initial target of infection by high risk HPV. Impact Journals LLC 2016-03-20 /pmc/articles/PMC5077987/ /pubmed/27008711 http://dx.doi.org/10.18632/oncotarget.8218 Text en Copyright: © 2016 Ortiz-Sánchez et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ortiz-Sánchez, Elizabeth
Santiago-López, Luz
Cruz-Domínguez, Verónica B.
Toledo-Guzmán, Mariel E.
Hernández-Cueto, Daniel
Muñiz-Hernández, Saé
Garrido, Efraín
De León, David Cantú
García-Carrancá, Alejandro
Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
title Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
title_full Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
title_fullStr Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
title_full_unstemmed Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
title_short Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
title_sort characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077987/
https://www.ncbi.nlm.nih.gov/pubmed/27008711
http://dx.doi.org/10.18632/oncotarget.8218
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