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Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties

Head and neck squamous carcinoma (HNSCC) tumors carry dismal long-term prognosis and the role of tumor initiating cells (TICs) in this cancer is unclear. We investigated in HNSCC xenografts whether specific tumor subpopulations contributed to tumor growth. We used a CFSE-based label retentions assay...

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Detalles Bibliográficos
Autores principales: Bragado, Paloma, Estrada, Yeriel, Sosa, Maria Soledad, Avivar-Valderas, Alvaro, Cannan, David, Genden, Eric, Teng, Marita, Ranganathan, Aparna C., Wen, Huei-Chi, Kapoor, Avnish, Bernstein, Emily, Aguirre-Ghiso, Julio A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262798/
https://www.ncbi.nlm.nih.gov/pubmed/22276135
http://dx.doi.org/10.1371/journal.pone.0029974
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author Bragado, Paloma
Estrada, Yeriel
Sosa, Maria Soledad
Avivar-Valderas, Alvaro
Cannan, David
Genden, Eric
Teng, Marita
Ranganathan, Aparna C.
Wen, Huei-Chi
Kapoor, Avnish
Bernstein, Emily
Aguirre-Ghiso, Julio A.
author_facet Bragado, Paloma
Estrada, Yeriel
Sosa, Maria Soledad
Avivar-Valderas, Alvaro
Cannan, David
Genden, Eric
Teng, Marita
Ranganathan, Aparna C.
Wen, Huei-Chi
Kapoor, Avnish
Bernstein, Emily
Aguirre-Ghiso, Julio A.
author_sort Bragado, Paloma
collection PubMed
description Head and neck squamous carcinoma (HNSCC) tumors carry dismal long-term prognosis and the role of tumor initiating cells (TICs) in this cancer is unclear. We investigated in HNSCC xenografts whether specific tumor subpopulations contributed to tumor growth. We used a CFSE-based label retentions assay, CD49f (α6-integrin) surface levels and aldehyde dehydrogenase (ALDH) activity to profile HNSCC subpopulations. The tumorigenic potential of marker-positive and -negative subpopulations was tested in nude (Balb/c nu/nu) and NSG (NOD.Cg-Prkdc(scid) Il2rg(tm1Wjl)/SzJ) mice and chicken embryo chorioallantoic membrane (CAM) assays. Here we identified in HEp3, SQ20b and FaDu HNSCC xenografts a subpopulation of G0/G1-arrested slow-cycling CD49f(high)/ALDH1A1(high)/H3K4/K27me3(low) subpopulation (CD49f+) of tumor cells. A strikingly similar CD49f(high)/H3K27me3(low) subpopulation is also present in primary human HNSCC tumors and metastases. While only sorted CD49f(high)/ALDH(high), label retaining cells (LRC) proliferated immediately in vivo, with time the CD49f(low)/ALDH(low), non-LRC (NLRC) tumor cell subpopulations were also able to regain tumorigenic capacity; this was linked to restoration of CD49f(high)/ALDH(high), label retaining cells. In addition, CD49f is required for HEp3 cell tumorigenicity and to maintain low levels of H3K4/K27me3. CD49f+ cells also displayed reduced expression of the histone-lysine N-methyltransferase EZH2 and ERK1/2phosphorylation. This suggests that although transiently quiescent, their unique chromatin structure is poised for rapid transcriptional activation. CD49f− cells can “reprogram” and also achieve this state eventually. We propose that in HNSCC tumors, epigenetic mechanisms likely driven by CD49f signaling dynamically regulate HNSCC xenograft phenotypic heterogeneity. This allows multiple tumor cell subpopulations to drive tumor growth suggesting that their dynamic nature renders them a “moving target” and their eradication might require more persistent strategies.
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spelling pubmed-32627982012-01-24 Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties Bragado, Paloma Estrada, Yeriel Sosa, Maria Soledad Avivar-Valderas, Alvaro Cannan, David Genden, Eric Teng, Marita Ranganathan, Aparna C. Wen, Huei-Chi Kapoor, Avnish Bernstein, Emily Aguirre-Ghiso, Julio A. PLoS One Research Article Head and neck squamous carcinoma (HNSCC) tumors carry dismal long-term prognosis and the role of tumor initiating cells (TICs) in this cancer is unclear. We investigated in HNSCC xenografts whether specific tumor subpopulations contributed to tumor growth. We used a CFSE-based label retentions assay, CD49f (α6-integrin) surface levels and aldehyde dehydrogenase (ALDH) activity to profile HNSCC subpopulations. The tumorigenic potential of marker-positive and -negative subpopulations was tested in nude (Balb/c nu/nu) and NSG (NOD.Cg-Prkdc(scid) Il2rg(tm1Wjl)/SzJ) mice and chicken embryo chorioallantoic membrane (CAM) assays. Here we identified in HEp3, SQ20b and FaDu HNSCC xenografts a subpopulation of G0/G1-arrested slow-cycling CD49f(high)/ALDH1A1(high)/H3K4/K27me3(low) subpopulation (CD49f+) of tumor cells. A strikingly similar CD49f(high)/H3K27me3(low) subpopulation is also present in primary human HNSCC tumors and metastases. While only sorted CD49f(high)/ALDH(high), label retaining cells (LRC) proliferated immediately in vivo, with time the CD49f(low)/ALDH(low), non-LRC (NLRC) tumor cell subpopulations were also able to regain tumorigenic capacity; this was linked to restoration of CD49f(high)/ALDH(high), label retaining cells. In addition, CD49f is required for HEp3 cell tumorigenicity and to maintain low levels of H3K4/K27me3. CD49f+ cells also displayed reduced expression of the histone-lysine N-methyltransferase EZH2 and ERK1/2phosphorylation. This suggests that although transiently quiescent, their unique chromatin structure is poised for rapid transcriptional activation. CD49f− cells can “reprogram” and also achieve this state eventually. We propose that in HNSCC tumors, epigenetic mechanisms likely driven by CD49f signaling dynamically regulate HNSCC xenograft phenotypic heterogeneity. This allows multiple tumor cell subpopulations to drive tumor growth suggesting that their dynamic nature renders them a “moving target” and their eradication might require more persistent strategies. Public Library of Science 2012-01-20 /pmc/articles/PMC3262798/ /pubmed/22276135 http://dx.doi.org/10.1371/journal.pone.0029974 Text en Bragado et al. http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Bragado, Paloma
Estrada, Yeriel
Sosa, Maria Soledad
Avivar-Valderas, Alvaro
Cannan, David
Genden, Eric
Teng, Marita
Ranganathan, Aparna C.
Wen, Huei-Chi
Kapoor, Avnish
Bernstein, Emily
Aguirre-Ghiso, Julio A.
Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties
title Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties
title_full Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties
title_fullStr Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties
title_full_unstemmed Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties
title_short Analysis of Marker-Defined HNSCC Subpopulations Reveals a Dynamic Regulation of Tumor Initiating Properties
title_sort analysis of marker-defined hnscc subpopulations reveals a dynamic regulation of tumor initiating properties
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262798/
https://www.ncbi.nlm.nih.gov/pubmed/22276135
http://dx.doi.org/10.1371/journal.pone.0029974
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