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 (ALDHbright)ac...
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creator | Ortiz-Sánchez, Elizabeth Santiago-López, Luz Cruz-Domínguez, Verónica B Toledo-Guzmán, Mariel E Hernández-Cueto, Daniel Muñiz-Hernández, Saé Garrido, Efraín Cantú De León, David García-Carrancá, Alejandro |
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 (ALDHbright)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 ALDHbright 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. |
doi_str_mv | 10.18632/oncotarget.8218 |
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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 (ALDHbright)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 ALDHbright 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.</description><identifier>ISSN: 1949-2553</identifier><identifier>EISSN: 1949-2553</identifier><identifier>DOI: 10.18632/oncotarget.8218</identifier><identifier>PMID: 27008711</identifier><language>eng</language><publisher>United States: Impact Journals LLC</publisher><subject>Aldehyde Dehydrogenase - metabolism ; Animals ; Annexin A2 - metabolism ; Biomarkers, Tumor - metabolism ; Female ; HeLa Cells ; Humans ; Integrin alpha6 - metabolism ; Keratin-17 - metabolism ; Mice, Inbred BALB C ; Mice, Nude ; Neoplastic Stem Cells - metabolism ; Neoplastic Stem Cells - pathology ; Phenotype ; Research Paper ; Spheroids, Cellular ; Transcription Factors - metabolism ; Tumor Suppressor Proteins - metabolism ; Uterine Cervical Neoplasms - metabolism ; Uterine Cervical Neoplasms - pathology</subject><ispartof>Oncotarget, 2016-05, Vol.7 (22), p.31943-31954</ispartof><rights>Copyright: © 2016 Ortiz-Sánchez et al. 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-ea7300b81a8a9e695e10e9fbac3da9fba65e4cc4fb560ceca9f66700b45319d93</citedby><cites>FETCH-LOGICAL-c354t-ea7300b81a8a9e695e10e9fbac3da9fba65e4cc4fb560ceca9f66700b45319d93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077987/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077987/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27008711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ortiz-Sánchez, Elizabeth</creatorcontrib><creatorcontrib>Santiago-López, Luz</creatorcontrib><creatorcontrib>Cruz-Domínguez, Verónica B</creatorcontrib><creatorcontrib>Toledo-Guzmán, Mariel E</creatorcontrib><creatorcontrib>Hernández-Cueto, Daniel</creatorcontrib><creatorcontrib>Muñiz-Hernández, Saé</creatorcontrib><creatorcontrib>Garrido, Efraín</creatorcontrib><creatorcontrib>Cantú De León, David</creatorcontrib><creatorcontrib>García-Carrancá, Alejandro</creatorcontrib><title>Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression</title><title>Oncotarget</title><addtitle>Oncotarget</addtitle><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 (ALDHbright)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 ALDHbright 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.</description><subject>Aldehyde Dehydrogenase - metabolism</subject><subject>Animals</subject><subject>Annexin A2 - metabolism</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Female</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Integrin alpha6 - metabolism</subject><subject>Keratin-17 - metabolism</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Neoplastic Stem Cells - pathology</subject><subject>Phenotype</subject><subject>Research Paper</subject><subject>Spheroids, Cellular</subject><subject>Transcription Factors - metabolism</subject><subject>Tumor Suppressor Proteins - metabolism</subject><subject>Uterine Cervical Neoplasms - metabolism</subject><subject>Uterine Cervical Neoplasms - pathology</subject><issn>1949-2553</issn><issn>1949-2553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUcFu1DAQtRCIVm3vnJCPHJpix3Fic0BCqxaQKvUCZ2vinewaEjvYzopy65_Xuy2lzGWexm_ejOcR8oazC65aUb8P3oYMcYP5QtVcvSDHXDe6qqUUL5_hI3KW0g9WQjadqvVrclR3jKmO82Nyt9pCBJsxuj-QXfA0DNRi3DkLI7XgC6Yp41SK41iN7iceUPpA5y36kG9n5zfnB4rHlM4p-DXdLhN4OsPsxjFMQHcuLonaUEW0OOcQKf6eY6GXgafk1QBjwrPHfEK-X11-W32prm8-f119uq6skE2uEDrBWK84KNDYaomcoR56sGIN-9xKbKxthl62zKIttbYt3-wbKbhea3FCPj7ozks_4dqizxFGM0c3Qbw1AZz5_8W7rdmEnZGs67TqisC7R4EYfi2Ysplc2t8CPIYlGa5qJrWou7pQ2QPVxpBSxOFpDGfmYJ75Z57Zm1da3j5f76nhr1XiHq09nWg</recordid><startdate>20160531</startdate><enddate>20160531</enddate><creator>Ortiz-Sánchez, Elizabeth</creator><creator>Santiago-López, Luz</creator><creator>Cruz-Domínguez, Verónica B</creator><creator>Toledo-Guzmán, Mariel E</creator><creator>Hernández-Cueto, Daniel</creator><creator>Muñiz-Hernández, Saé</creator><creator>Garrido, Efraín</creator><creator>Cantú De León, David</creator><creator>García-Carrancá, Alejandro</creator><general>Impact Journals LLC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160531</creationdate><title>Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression</title><author>Ortiz-Sánchez, Elizabeth ; Santiago-López, Luz ; Cruz-Domínguez, Verónica B ; Toledo-Guzmán, Mariel E ; Hernández-Cueto, Daniel ; Muñiz-Hernández, Saé ; Garrido, Efraín ; Cantú De León, David ; García-Carrancá, Alejandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-ea7300b81a8a9e695e10e9fbac3da9fba65e4cc4fb560ceca9f66700b45319d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aldehyde Dehydrogenase - metabolism</topic><topic>Animals</topic><topic>Annexin A2 - metabolism</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Female</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Integrin alpha6 - metabolism</topic><topic>Keratin-17 - metabolism</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Neoplastic Stem Cells - pathology</topic><topic>Phenotype</topic><topic>Research Paper</topic><topic>Spheroids, Cellular</topic><topic>Transcription Factors - metabolism</topic><topic>Tumor Suppressor Proteins - metabolism</topic><topic>Uterine Cervical Neoplasms - metabolism</topic><topic>Uterine Cervical Neoplasms - pathology</topic><toplevel>online_resources</toplevel><creatorcontrib>Ortiz-Sánchez, Elizabeth</creatorcontrib><creatorcontrib>Santiago-López, Luz</creatorcontrib><creatorcontrib>Cruz-Domínguez, Verónica B</creatorcontrib><creatorcontrib>Toledo-Guzmán, Mariel E</creatorcontrib><creatorcontrib>Hernández-Cueto, Daniel</creatorcontrib><creatorcontrib>Muñiz-Hernández, Saé</creatorcontrib><creatorcontrib>Garrido, Efraín</creatorcontrib><creatorcontrib>Cantú De León, David</creatorcontrib><creatorcontrib>García-Carrancá, Alejandro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncotarget</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ortiz-Sánchez, Elizabeth</au><au>Santiago-López, Luz</au><au>Cruz-Domínguez, Verónica B</au><au>Toledo-Guzmán, Mariel E</au><au>Hernández-Cueto, Daniel</au><au>Muñiz-Hernández, Saé</au><au>Garrido, Efraín</au><au>Cantú De León, David</au><au>García-Carrancá, Alejandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression</atitle><jtitle>Oncotarget</jtitle><addtitle>Oncotarget</addtitle><date>2016-05-31</date><risdate>2016</risdate><volume>7</volume><issue>22</issue><spage>31943</spage><epage>31954</epage><pages>31943-31954</pages><issn>1949-2553</issn><eissn>1949-2553</eissn><abstract>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 (ALDHbright)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 ALDHbright 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.</abstract><cop>United States</cop><pub>Impact Journals LLC</pub><pmid>27008711</pmid><doi>10.18632/oncotarget.8218</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aldehyde Dehydrogenase - metabolism Animals Annexin A2 - metabolism Biomarkers, Tumor - metabolism Female HeLa Cells Humans Integrin alpha6 - metabolism Keratin-17 - metabolism Mice, Inbred BALB C Mice, Nude Neoplastic Stem Cells - metabolism Neoplastic Stem Cells - pathology Phenotype Research Paper Spheroids, Cellular Transcription Factors - metabolism Tumor Suppressor Proteins - metabolism Uterine Cervical Neoplasms - metabolism Uterine Cervical Neoplasms - pathology |
title | Characterization of cervical cancer stem cell-like cells: phenotyping, stemness, and human papilloma virus co-receptor expression |
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