Cargando…
Promoter Methylation Status of Survival-Related Genes in MOLT- 4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells under Hypoxic Conditions
OBJECTIVE: DNA methylation is a well-studied epigenetic mechanism that is a potent arm of the gene expression controlling machinery. Since the hypoxic situation and the various cells of bone marrow microenvironment, e.g. mesenchymal stem cells, play a role in the in vivo and in vitro biology of leuk...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893290/ https://www.ncbi.nlm.nih.gov/pubmed/29633596 http://dx.doi.org/10.22074/cellj.2018.5101 |
_version_ | 1783313291027677184 |
---|---|
author | Ahani-Nahayati, Milad Solali, Saeed Shams Asenjan, Karim Movassaghpour Akbari, Ali Akbar Talebi, Mehdi Zadi Heydarabad, Milad Baharaghdam, Sina Farshdousti Hagh, Majid |
author_facet | Ahani-Nahayati, Milad Solali, Saeed Shams Asenjan, Karim Movassaghpour Akbari, Ali Akbar Talebi, Mehdi Zadi Heydarabad, Milad Baharaghdam, Sina Farshdousti Hagh, Majid |
author_sort | Ahani-Nahayati, Milad |
collection | PubMed |
description | OBJECTIVE: DNA methylation is a well-studied epigenetic mechanism that is a potent arm of the gene expression controlling machinery. Since the hypoxic situation and the various cells of bone marrow microenvironment, e.g. mesenchymal stem cells, play a role in the in vivo and in vitro biology of leukemic cells, we decided to study the effects of hypoxia and mesenchymal stem cells (MSCs) on the promoter methylation pattern of BAX and BCL2 genes. MATERIALS AND METHODS: In this experimental study, the co-culture of MOLT-4 cells with MSCs and treatment with CoCl(2) was done during 6, 12, and 24 hour periods. Total DNA was extracted using commercial DNA extraction kits, and sodium bisulfite (SBS) treatment was performed on the extracted DNA. Methylation specific polymerase chain reaction (MSP) was used to evaluate the methylation status of the selected genes’ promoter regions. RESULTS: The BAX and BCL2 promoters of untreated MOLT-4 cells were in partial methylated and fully unmethylated states, respectively. After incubating the cancer cells with CoCl(2)and MSCs, the MSP results after 6, 12, and 24 hours were the same as untreated MOLT-4 cells. In other words, the exposure of MOLT-4 cells to the hypoxia-mimicry agent and MSCs in various modes and different time frames showed that these factors have exerted no change on the methylation signature of the studied fragments from the promoter region of the mentioned genes. CONCLUSION: Hypoxia and MSCs actually have no notable effect on the methylation status of the promoters of BAX and BCL2 in the specifically studied regions. DNA methylation is probably not the main process by which MSCs and CoCl(2) induced hypoxia regulate the expression of these genes. Finally, we are still far from discovering the exact functional mechanisms of gene expression directors, but these investigations can provide new insights into this field for upcoming studies. |
format | Online Article Text |
id | pubmed-5893290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-58932902018-07-01 Promoter Methylation Status of Survival-Related Genes in MOLT- 4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells under Hypoxic Conditions Ahani-Nahayati, Milad Solali, Saeed Shams Asenjan, Karim Movassaghpour Akbari, Ali Akbar Talebi, Mehdi Zadi Heydarabad, Milad Baharaghdam, Sina Farshdousti Hagh, Majid Cell J Original Article OBJECTIVE: DNA methylation is a well-studied epigenetic mechanism that is a potent arm of the gene expression controlling machinery. Since the hypoxic situation and the various cells of bone marrow microenvironment, e.g. mesenchymal stem cells, play a role in the in vivo and in vitro biology of leukemic cells, we decided to study the effects of hypoxia and mesenchymal stem cells (MSCs) on the promoter methylation pattern of BAX and BCL2 genes. MATERIALS AND METHODS: In this experimental study, the co-culture of MOLT-4 cells with MSCs and treatment with CoCl(2) was done during 6, 12, and 24 hour periods. Total DNA was extracted using commercial DNA extraction kits, and sodium bisulfite (SBS) treatment was performed on the extracted DNA. Methylation specific polymerase chain reaction (MSP) was used to evaluate the methylation status of the selected genes’ promoter regions. RESULTS: The BAX and BCL2 promoters of untreated MOLT-4 cells were in partial methylated and fully unmethylated states, respectively. After incubating the cancer cells with CoCl(2)and MSCs, the MSP results after 6, 12, and 24 hours were the same as untreated MOLT-4 cells. In other words, the exposure of MOLT-4 cells to the hypoxia-mimicry agent and MSCs in various modes and different time frames showed that these factors have exerted no change on the methylation signature of the studied fragments from the promoter region of the mentioned genes. CONCLUSION: Hypoxia and MSCs actually have no notable effect on the methylation status of the promoters of BAX and BCL2 in the specifically studied regions. DNA methylation is probably not the main process by which MSCs and CoCl(2) induced hypoxia regulate the expression of these genes. Finally, we are still far from discovering the exact functional mechanisms of gene expression directors, but these investigations can provide new insights into this field for upcoming studies. Royan Institute 2018 2018-03-18 /pmc/articles/PMC5893290/ /pubmed/29633596 http://dx.doi.org/10.22074/cellj.2018.5101 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited 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 work is properly cited. |
spellingShingle | Original Article Ahani-Nahayati, Milad Solali, Saeed Shams Asenjan, Karim Movassaghpour Akbari, Ali Akbar Talebi, Mehdi Zadi Heydarabad, Milad Baharaghdam, Sina Farshdousti Hagh, Majid Promoter Methylation Status of Survival-Related Genes in MOLT- 4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells under Hypoxic Conditions |
title | Promoter Methylation Status of Survival-Related Genes in MOLT-
4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells
under Hypoxic Conditions |
title_full | Promoter Methylation Status of Survival-Related Genes in MOLT-
4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells
under Hypoxic Conditions |
title_fullStr | Promoter Methylation Status of Survival-Related Genes in MOLT-
4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells
under Hypoxic Conditions |
title_full_unstemmed | Promoter Methylation Status of Survival-Related Genes in MOLT-
4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells
under Hypoxic Conditions |
title_short | Promoter Methylation Status of Survival-Related Genes in MOLT-
4 Cells Co-Cultured with Bone Marrow Mesenchymal Stem Cells
under Hypoxic Conditions |
title_sort | promoter methylation status of survival-related genes in molt-
4 cells co-cultured with bone marrow mesenchymal stem cells
under hypoxic conditions |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893290/ https://www.ncbi.nlm.nih.gov/pubmed/29633596 http://dx.doi.org/10.22074/cellj.2018.5101 |
work_keys_str_mv | AT ahaninahayatimilad promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT solalisaeed promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT shamsasenjankarim promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT movassaghpourakbarialiakbar promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT talebimehdi promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT zadiheydarabadmilad promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT baharaghdamsina promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions AT farshdoustihaghmajid promotermethylationstatusofsurvivalrelatedgenesinmolt4cellscoculturedwithbonemarrowmesenchymalstemcellsunderhypoxicconditions |