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The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping
BACKGROUND: BCL-2 is the most important anti-apoptotic regulator and Bax is a pro-apoptotic protein. The status of these parameters or the ration of BCL-2 to BAX is important in malignant cell fate as well as normal cells. METHODS: Sixty-two ALL patients and 62 healthy sex-and age-matched controls w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Babol University of Medical Sciences
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913713/ https://www.ncbi.nlm.nih.gov/pubmed/27386062 |
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author | Moazami-Goudarzi, Mozhagan Farshdousti-Hagh, Majid Hoseinpour-Feizi, Abbasali Talebi, Mehdi Movassaghpour-Akbari, Ali Akbar Shams-Asanjan, Karim Eyvazi-Ziyaee, Jamal Seifi, Morteza |
author_facet | Moazami-Goudarzi, Mozhagan Farshdousti-Hagh, Majid Hoseinpour-Feizi, Abbasali Talebi, Mehdi Movassaghpour-Akbari, Ali Akbar Shams-Asanjan, Karim Eyvazi-Ziyaee, Jamal Seifi, Morteza |
author_sort | Moazami-Goudarzi, Mozhagan |
collection | PubMed |
description | BACKGROUND: BCL-2 is the most important anti-apoptotic regulator and Bax is a pro-apoptotic protein. The status of these parameters or the ration of BCL-2 to BAX is important in malignant cell fate as well as normal cells. METHODS: Sixty-two ALL patients and 62 healthy sex-and age-matched controls were studied. After genotyping, the promoter region of the BAX and BCL-2 genes by RFLP-PCR method the patients were classified in nine prognostic groups, after that, the overall survival ratio of each score was compared with others pair-wise or between groups. RESULTS: The frequencies of the AA, AC, CC alleles of the BCL-2 C-938A polymorphism in patient group were 33 (53.23%), 18 (29.03%), 11 (17.74%), and in the control group were 13 (21.0%), 27 (43.5%), 22 (35.5%), respectively (P=0.003). Also, the frequencies of AA, AG, GG alleles of the BAX G-248A SNP were 15 (24.2%), 24 (38.7%), 23 (37.1%) in ALL group and 13 (21.0%), 25 (40.3%), 24 (38.7%) (p>0.05) in the control group. The survival time estimation and ratio were significantly different between different SNPs in BCL-2 (P=0.002). CONCLUSION: These findings showed that the BCL-2 promoter region polymorphism is more reliable than BAX gene promoter polymorphism in any ALL scoring system. But the establishment of complete scoring system requires further more clinical and laboratory findings along with genetic polymorphisms is necessary. |
format | Online Article Text |
id | pubmed-4913713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Babol University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-49137132016-07-06 The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping Moazami-Goudarzi, Mozhagan Farshdousti-Hagh, Majid Hoseinpour-Feizi, Abbasali Talebi, Mehdi Movassaghpour-Akbari, Ali Akbar Shams-Asanjan, Karim Eyvazi-Ziyaee, Jamal Seifi, Morteza Caspian J Intern Med Original Article BACKGROUND: BCL-2 is the most important anti-apoptotic regulator and Bax is a pro-apoptotic protein. The status of these parameters or the ration of BCL-2 to BAX is important in malignant cell fate as well as normal cells. METHODS: Sixty-two ALL patients and 62 healthy sex-and age-matched controls were studied. After genotyping, the promoter region of the BAX and BCL-2 genes by RFLP-PCR method the patients were classified in nine prognostic groups, after that, the overall survival ratio of each score was compared with others pair-wise or between groups. RESULTS: The frequencies of the AA, AC, CC alleles of the BCL-2 C-938A polymorphism in patient group were 33 (53.23%), 18 (29.03%), 11 (17.74%), and in the control group were 13 (21.0%), 27 (43.5%), 22 (35.5%), respectively (P=0.003). Also, the frequencies of AA, AG, GG alleles of the BAX G-248A SNP were 15 (24.2%), 24 (38.7%), 23 (37.1%) in ALL group and 13 (21.0%), 25 (40.3%), 24 (38.7%) (p>0.05) in the control group. The survival time estimation and ratio were significantly different between different SNPs in BCL-2 (P=0.002). CONCLUSION: These findings showed that the BCL-2 promoter region polymorphism is more reliable than BAX gene promoter polymorphism in any ALL scoring system. But the establishment of complete scoring system requires further more clinical and laboratory findings along with genetic polymorphisms is necessary. Babol University of Medical Sciences 2016 /pmc/articles/PMC4913713/ /pubmed/27386062 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Moazami-Goudarzi, Mozhagan Farshdousti-Hagh, Majid Hoseinpour-Feizi, Abbasali Talebi, Mehdi Movassaghpour-Akbari, Ali Akbar Shams-Asanjan, Karim Eyvazi-Ziyaee, Jamal Seifi, Morteza The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping |
title | The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping |
title_full | The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping |
title_fullStr | The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping |
title_full_unstemmed | The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping |
title_short | The acute lymphoblastic leukemia prognostic scoring whether it is possible by BCL-2, BAX gene promoter genotyping |
title_sort | acute lymphoblastic leukemia prognostic scoring whether it is possible by bcl-2, bax gene promoter genotyping |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913713/ https://www.ncbi.nlm.nih.gov/pubmed/27386062 |
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