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Histone Modification Marks Strongly Regulate CDH1 Promoter in Prostospheres as A Model of Prostate Cancer Stem Like Cells
OBJECTIVE: Cadherin-1 (CDH1) plays an important role in the metastasis, while expression of this protein is under control of epigenetic changes on its gene promoter. Therefore we evaluated both DNA methylation (DNAmet) and histone modification marks of CDH1 in prostate cancer stem like cells (PCSLCs...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397603/ https://www.ncbi.nlm.nih.gov/pubmed/30825285 http://dx.doi.org/10.22074/cellj.2019.5702 |
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author | Shokraii, Fatemeh Moharrami, Maryam Motamed, Nasrin Shahhoseini, Maryam Totonchi, Mehdi Ezzatizadeh, Vahid Firouzi, Javad Khosravani, Pardis Ebrahimi, Marzieh |
author_facet | Shokraii, Fatemeh Moharrami, Maryam Motamed, Nasrin Shahhoseini, Maryam Totonchi, Mehdi Ezzatizadeh, Vahid Firouzi, Javad Khosravani, Pardis Ebrahimi, Marzieh |
author_sort | Shokraii, Fatemeh |
collection | PubMed |
description | OBJECTIVE: Cadherin-1 (CDH1) plays an important role in the metastasis, while expression of this protein is under control of epigenetic changes on its gene promoter. Therefore we evaluated both DNA methylation (DNAmet) and histone modification marks of CDH1 in prostate cancer stem like cells (PCSLCs). MATERIALS AND METHODS: In this experimental study, we isolated PCSLCs using cell surface marker and prostaspheroid formation, respectively. The cells isolated from both methods were characterized and then the levels of H3K4me2, H3K27me3, H3K9me2/3 and H3K9ac as well as DNAmet were assessed in CDH1 promoter of the isolated cells. RESULTS: The CD44(+) CD49(hi) cells were not validated as PCSLCs. However, prostaspheres overexpressed stemness related genes and had higher ability of invasion potential, associated with reduction in CDH1 expression. Epigenetic status analysis showed that CDH1 promoter was hypo-methylated. Histone modifications of H3K9ac and H3K4me3 were significantly reduced, in parallel with an increased level of H3K27me3. CONCLUSION: Our results suggest that slight decrease of DNAmet of the CpG island in CDH1 promoter does not significantly contribute to the change of CDH1 expression. Therefore, histone modifications are responsible in repressing CDH1 in PCSLCs. |
format | Online Article Text |
id | pubmed-6397603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-63976032019-07-01 Histone Modification Marks Strongly Regulate CDH1 Promoter in Prostospheres as A Model of Prostate Cancer Stem Like Cells Shokraii, Fatemeh Moharrami, Maryam Motamed, Nasrin Shahhoseini, Maryam Totonchi, Mehdi Ezzatizadeh, Vahid Firouzi, Javad Khosravani, Pardis Ebrahimi, Marzieh Cell J Original Article OBJECTIVE: Cadherin-1 (CDH1) plays an important role in the metastasis, while expression of this protein is under control of epigenetic changes on its gene promoter. Therefore we evaluated both DNA methylation (DNAmet) and histone modification marks of CDH1 in prostate cancer stem like cells (PCSLCs). MATERIALS AND METHODS: In this experimental study, we isolated PCSLCs using cell surface marker and prostaspheroid formation, respectively. The cells isolated from both methods were characterized and then the levels of H3K4me2, H3K27me3, H3K9me2/3 and H3K9ac as well as DNAmet were assessed in CDH1 promoter of the isolated cells. RESULTS: The CD44(+) CD49(hi) cells were not validated as PCSLCs. However, prostaspheres overexpressed stemness related genes and had higher ability of invasion potential, associated with reduction in CDH1 expression. Epigenetic status analysis showed that CDH1 promoter was hypo-methylated. Histone modifications of H3K9ac and H3K4me3 were significantly reduced, in parallel with an increased level of H3K27me3. CONCLUSION: Our results suggest that slight decrease of DNAmet of the CpG island in CDH1 promoter does not significantly contribute to the change of CDH1 expression. Therefore, histone modifications are responsible in repressing CDH1 in PCSLCs. Royan Institute 2019 2019-02-25 /pmc/articles/PMC6397603/ /pubmed/30825285 http://dx.doi.org/10.22074/cellj.2019.5702 Text en The Cell Journal (Yakhteh) is an open access journal which means the articles are freely available online for any individual author to download and use the providing address. http://creativecommons.org/licenses/by/3.0/ The journal is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported License which allows the author(s) to hold the copyright without restrictions that is permitting unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited. |
spellingShingle | Original Article Shokraii, Fatemeh Moharrami, Maryam Motamed, Nasrin Shahhoseini, Maryam Totonchi, Mehdi Ezzatizadeh, Vahid Firouzi, Javad Khosravani, Pardis Ebrahimi, Marzieh Histone Modification Marks Strongly Regulate CDH1 Promoter in Prostospheres as A Model of Prostate Cancer Stem Like Cells |
title | Histone Modification Marks Strongly Regulate CDH1 Promoter in
Prostospheres as A Model of Prostate Cancer Stem Like Cells |
title_full | Histone Modification Marks Strongly Regulate CDH1 Promoter in
Prostospheres as A Model of Prostate Cancer Stem Like Cells |
title_fullStr | Histone Modification Marks Strongly Regulate CDH1 Promoter in
Prostospheres as A Model of Prostate Cancer Stem Like Cells |
title_full_unstemmed | Histone Modification Marks Strongly Regulate CDH1 Promoter in
Prostospheres as A Model of Prostate Cancer Stem Like Cells |
title_short | Histone Modification Marks Strongly Regulate CDH1 Promoter in
Prostospheres as A Model of Prostate Cancer Stem Like Cells |
title_sort | histone modification marks strongly regulate cdh1 promoter in
prostospheres as a model of prostate cancer stem like cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397603/ https://www.ncbi.nlm.nih.gov/pubmed/30825285 http://dx.doi.org/10.22074/cellj.2019.5702 |
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