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The significance of low PU.1 expression in patients with acute promyelocytic leukemia
BACKGROUND: Although the importance of the hematopoietic transcription factor PU.1 in acute myeloid leukemia (AML) has been demonstrated, the expression of PU.1 in acute promyelocytic leukemia (APL) patient samples awaits further investigation. The current study used APL patient samples to assess th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407792/ https://www.ncbi.nlm.nih.gov/pubmed/22569057 http://dx.doi.org/10.1186/1756-8722-5-22 |
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author | Zhu, Xuehua Zhang, Hui Qian, Maoxiang Zhao, Xujie Yang, Wentao Wang, Ping Zhang, Ji Wang, Kankan |
author_facet | Zhu, Xuehua Zhang, Hui Qian, Maoxiang Zhao, Xujie Yang, Wentao Wang, Ping Zhang, Ji Wang, Kankan |
author_sort | Zhu, Xuehua |
collection | PubMed |
description | BACKGROUND: Although the importance of the hematopoietic transcription factor PU.1 in acute myeloid leukemia (AML) has been demonstrated, the expression of PU.1 in acute promyelocytic leukemia (APL) patient samples awaits further investigation. The current study used APL patient samples to assess the expression pattern of PU.1 in the initiation and progression of APL. FINDINGS: We used real-time RT-PCR to compare PU.1 expression between de novo APL patient samples and normal blood specimens, and the results indicated that PU.1 expression was significantly lower in newly diagnosed APL patient samples as compared to normal hematopoietic cells. Further evidence showed a significant inverse correlation between the expression level of PML-RARα and that of PU.1. In addition, we analyzed the correlation between PML-RARα and PU.1 expression in a large population of AML patients retrieved from the expression profiles. The results showed that PU.1 expression was lower in patients with APL than other AML subtypes and there was also a trend towards increasing PU.1 expression from AML-M0 to AML-M5, with the exception of AML-M3 (APL). These observations suggested that PU.1 expression was reduced by PML-RARα in APL patients. Furthermore, we measured PU.1 expression in APL-initiating cells isolated from de novo APL patients by side population cell analysis and found that suppression of PU.1 expression occurred concurrently with PML-RARα expression, indicating the pivotal role of PU.1 in APL initiation. CONCLUSION: Our findings provide evidence that low PU.1 expression in APL patients is required for disease initiation and progression. |
format | Online Article Text |
id | pubmed-3407792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34077922012-07-30 The significance of low PU.1 expression in patients with acute promyelocytic leukemia Zhu, Xuehua Zhang, Hui Qian, Maoxiang Zhao, Xujie Yang, Wentao Wang, Ping Zhang, Ji Wang, Kankan J Hematol Oncol Rapid Communication BACKGROUND: Although the importance of the hematopoietic transcription factor PU.1 in acute myeloid leukemia (AML) has been demonstrated, the expression of PU.1 in acute promyelocytic leukemia (APL) patient samples awaits further investigation. The current study used APL patient samples to assess the expression pattern of PU.1 in the initiation and progression of APL. FINDINGS: We used real-time RT-PCR to compare PU.1 expression between de novo APL patient samples and normal blood specimens, and the results indicated that PU.1 expression was significantly lower in newly diagnosed APL patient samples as compared to normal hematopoietic cells. Further evidence showed a significant inverse correlation between the expression level of PML-RARα and that of PU.1. In addition, we analyzed the correlation between PML-RARα and PU.1 expression in a large population of AML patients retrieved from the expression profiles. The results showed that PU.1 expression was lower in patients with APL than other AML subtypes and there was also a trend towards increasing PU.1 expression from AML-M0 to AML-M5, with the exception of AML-M3 (APL). These observations suggested that PU.1 expression was reduced by PML-RARα in APL patients. Furthermore, we measured PU.1 expression in APL-initiating cells isolated from de novo APL patients by side population cell analysis and found that suppression of PU.1 expression occurred concurrently with PML-RARα expression, indicating the pivotal role of PU.1 in APL initiation. CONCLUSION: Our findings provide evidence that low PU.1 expression in APL patients is required for disease initiation and progression. BioMed Central 2012-05-08 /pmc/articles/PMC3407792/ /pubmed/22569057 http://dx.doi.org/10.1186/1756-8722-5-22 Text en Copyright ©2012 Zhu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Rapid Communication Zhu, Xuehua Zhang, Hui Qian, Maoxiang Zhao, Xujie Yang, Wentao Wang, Ping Zhang, Ji Wang, Kankan The significance of low PU.1 expression in patients with acute promyelocytic leukemia |
title | The significance of low PU.1 expression in patients with acute promyelocytic leukemia |
title_full | The significance of low PU.1 expression in patients with acute promyelocytic leukemia |
title_fullStr | The significance of low PU.1 expression in patients with acute promyelocytic leukemia |
title_full_unstemmed | The significance of low PU.1 expression in patients with acute promyelocytic leukemia |
title_short | The significance of low PU.1 expression in patients with acute promyelocytic leukemia |
title_sort | significance of low pu.1 expression in patients with acute promyelocytic leukemia |
topic | Rapid Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407792/ https://www.ncbi.nlm.nih.gov/pubmed/22569057 http://dx.doi.org/10.1186/1756-8722-5-22 |
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