Cargando…
Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells
BACKGROUND: One of the most significant problems in the treatment of leukemia is the expansion of resistance to chemotherapeutic agents. Therefore, assessing the drug resistance and especially the drug resistance genes of leukemic cells is important in any treatment. The impact of Mesenchymal Stem C...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Avicenna Research Institute
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960061/ https://www.ncbi.nlm.nih.gov/pubmed/29849981 |
_version_ | 1783324515415097344 |
---|---|
author | Baharaghdam, Sina Yousefi, Mehdi Movasaghpour, Aliakbar Solali, Saeed Talebi, Mehdi Ahani-Nahayati, Milad Lotfimehr, Hamid Shamsasanjan, Karim |
author_facet | Baharaghdam, Sina Yousefi, Mehdi Movasaghpour, Aliakbar Solali, Saeed Talebi, Mehdi Ahani-Nahayati, Milad Lotfimehr, Hamid Shamsasanjan, Karim |
author_sort | Baharaghdam, Sina |
collection | PubMed |
description | BACKGROUND: One of the most significant problems in the treatment of leukemia is the expansion of resistance to chemotherapeutic agents. Therefore, assessing the drug resistance and especially the drug resistance genes of leukemic cells is important in any treatment. The impact of Mesenchymal Stem Cells (MSCs) and hypoxic condition have been observed in the biological performance of majority of leukemic cells. METHODS: MOLT-4 cells were co-cultured with MSCs in the hypoxic condition induced by Cobalt Chloride (CoCl(2)) for 6 and 24 hr. Then, apoptosis of cells was analyzed using annexin-V/PI staining and expression of the drug resistance genes including MDR1, MRP, and BCRP along with apoptotic and anti-apoptotic genes, including BAX and BCL2, was evaluated by real-time PCR. RESULTS: The hypoxic condition for MOLT-4 cells co-cultured with MSCs could significantly increase the expression of MDR1 and BCRP genes (p<0.05) which are involved in drug resistance. Also, the results indicated that this condition significantly increases the expression of BCL2 (p<0.05) and reduces the apoptosis in MOLT-4 cells co-cultured with MSCs in the hypoxic condition. CONCLUSION: These effects can demonstrate the important role of hypoxia and MSCs on the biological behavior of Acute Lymphoblastic Leukemia (ALL) cells that may lead to particular treatment outcomes. |
format | Online Article Text |
id | pubmed-5960061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Avicenna Research Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-59600612018-05-30 Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells Baharaghdam, Sina Yousefi, Mehdi Movasaghpour, Aliakbar Solali, Saeed Talebi, Mehdi Ahani-Nahayati, Milad Lotfimehr, Hamid Shamsasanjan, Karim Avicenna J Med Biotechnol Original Article BACKGROUND: One of the most significant problems in the treatment of leukemia is the expansion of resistance to chemotherapeutic agents. Therefore, assessing the drug resistance and especially the drug resistance genes of leukemic cells is important in any treatment. The impact of Mesenchymal Stem Cells (MSCs) and hypoxic condition have been observed in the biological performance of majority of leukemic cells. METHODS: MOLT-4 cells were co-cultured with MSCs in the hypoxic condition induced by Cobalt Chloride (CoCl(2)) for 6 and 24 hr. Then, apoptosis of cells was analyzed using annexin-V/PI staining and expression of the drug resistance genes including MDR1, MRP, and BCRP along with apoptotic and anti-apoptotic genes, including BAX and BCL2, was evaluated by real-time PCR. RESULTS: The hypoxic condition for MOLT-4 cells co-cultured with MSCs could significantly increase the expression of MDR1 and BCRP genes (p<0.05) which are involved in drug resistance. Also, the results indicated that this condition significantly increases the expression of BCL2 (p<0.05) and reduces the apoptosis in MOLT-4 cells co-cultured with MSCs in the hypoxic condition. CONCLUSION: These effects can demonstrate the important role of hypoxia and MSCs on the biological behavior of Acute Lymphoblastic Leukemia (ALL) cells that may lead to particular treatment outcomes. Avicenna Research Institute 2018 /pmc/articles/PMC5960061/ /pubmed/29849981 Text en Copyright© 2018 Avicenna Research Institute http://creativecommons.org/licenses/by/3.0/ 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 work is properly cited. |
spellingShingle | Original Article Baharaghdam, Sina Yousefi, Mehdi Movasaghpour, Aliakbar Solali, Saeed Talebi, Mehdi Ahani-Nahayati, Milad Lotfimehr, Hamid Shamsasanjan, Karim Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells |
title | Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells |
title_full | Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells |
title_fullStr | Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells |
title_full_unstemmed | Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells |
title_short | Effects of Hypoxia on Biology of Human Leukemia T-cell Line (MOLT-4 cells) Co-cultured with Bone Marrow Mesenchymal Stem Cells |
title_sort | effects of hypoxia on biology of human leukemia t-cell line (molt-4 cells) co-cultured with bone marrow mesenchymal stem cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960061/ https://www.ncbi.nlm.nih.gov/pubmed/29849981 |
work_keys_str_mv | AT baharaghdamsina effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT yousefimehdi effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT movasaghpouraliakbar effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT solalisaeed effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT talebimehdi effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT ahaninahayatimilad effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT lotfimehrhamid effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells AT shamsasanjankarim effectsofhypoxiaonbiologyofhumanleukemiatcelllinemolt4cellscoculturedwithbonemarrowmesenchymalstemcells |