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Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells

The Facilitates Chromatin Transcription (FACT) chromatin remodeling complex, comprised of two subunits, SSRP1 and SPT16, is involved in transcription, replication and DNA repair. We recently showed that curaxins, small molecules with anti-cancer activity, target FACT and kill tumor cells in a FACT-d...

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Autores principales: Garcia, Henry, Fleyshman, Daria, Kolesnikova, Katerina, Safina, Alfiya, Commane, Mairead, Paszkiewicz, Geraldine, Omelian, Angela, Morrison, Carl, Gurova, Kateryna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248156/
https://www.ncbi.nlm.nih.gov/pubmed/21998152
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author Garcia, Henry
Fleyshman, Daria
Kolesnikova, Katerina
Safina, Alfiya
Commane, Mairead
Paszkiewicz, Geraldine
Omelian, Angela
Morrison, Carl
Gurova, Kateryna
author_facet Garcia, Henry
Fleyshman, Daria
Kolesnikova, Katerina
Safina, Alfiya
Commane, Mairead
Paszkiewicz, Geraldine
Omelian, Angela
Morrison, Carl
Gurova, Kateryna
author_sort Garcia, Henry
collection PubMed
description The Facilitates Chromatin Transcription (FACT) chromatin remodeling complex, comprised of two subunits, SSRP1 and SPT16, is involved in transcription, replication and DNA repair. We recently showed that curaxins, small molecules with anti-cancer activity, target FACT and kill tumor cells in a FACT-dependent manner. We also found that FACT is overexpressed in human and mouse tumors and that tumor cells are sensitive to FACT downregulation. To clarify the clinical potential of FACT inhibition, we were interested in physiological role(s) of FACT in multicellular organisms. We analyzed SSRP1 and SPT16 expression in different cells, tissues and conditions using Immunohistochemical (IHC) staining of mouse and human tissues and analysis of publically available high-content gene expression datasets. Both approaches demonstrated coordinated expression of the two FACT subunits, which was primarily associated with the stage of cellular differentiation. Most cells of adult tissues do not have detectable protein level of FACT. High FACT expression was associated with stem or less-differentiated cells, while low FACT levels were seen in more differentiated cells. Experimental manipulation of cell differentiation and proliferation in vitro, as well as tissue staining for the Ki67 proliferation marker, showed that FACT expression is related more to differentiation than to proliferation. Thus, FACT may be part of a stem cell-like gene expression signature and play a role in maintaining cells in an undifferentiated state, which is consistent with its potential role as an anti-cancer target.
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spelling pubmed-32481562012-01-18 Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells Garcia, Henry Fleyshman, Daria Kolesnikova, Katerina Safina, Alfiya Commane, Mairead Paszkiewicz, Geraldine Omelian, Angela Morrison, Carl Gurova, Kateryna Oncotarget Research Papers The Facilitates Chromatin Transcription (FACT) chromatin remodeling complex, comprised of two subunits, SSRP1 and SPT16, is involved in transcription, replication and DNA repair. We recently showed that curaxins, small molecules with anti-cancer activity, target FACT and kill tumor cells in a FACT-dependent manner. We also found that FACT is overexpressed in human and mouse tumors and that tumor cells are sensitive to FACT downregulation. To clarify the clinical potential of FACT inhibition, we were interested in physiological role(s) of FACT in multicellular organisms. We analyzed SSRP1 and SPT16 expression in different cells, tissues and conditions using Immunohistochemical (IHC) staining of mouse and human tissues and analysis of publically available high-content gene expression datasets. Both approaches demonstrated coordinated expression of the two FACT subunits, which was primarily associated with the stage of cellular differentiation. Most cells of adult tissues do not have detectable protein level of FACT. High FACT expression was associated with stem or less-differentiated cells, while low FACT levels were seen in more differentiated cells. Experimental manipulation of cell differentiation and proliferation in vitro, as well as tissue staining for the Ki67 proliferation marker, showed that FACT expression is related more to differentiation than to proliferation. Thus, FACT may be part of a stem cell-like gene expression signature and play a role in maintaining cells in an undifferentiated state, which is consistent with its potential role as an anti-cancer target. Impact Journals LLC 2011-10-13 /pmc/articles/PMC3248156/ /pubmed/21998152 Text en Copyright: © 2011 Garcia 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 Papers
Garcia, Henry
Fleyshman, Daria
Kolesnikova, Katerina
Safina, Alfiya
Commane, Mairead
Paszkiewicz, Geraldine
Omelian, Angela
Morrison, Carl
Gurova, Kateryna
Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
title Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
title_full Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
title_fullStr Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
title_full_unstemmed Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
title_short Expression of FACT in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
title_sort expression of fact in mammalian tissues suggests its role in maintaining of undifferentiated state of cells
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248156/
https://www.ncbi.nlm.nih.gov/pubmed/21998152
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