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RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression
BACKGROUND: RIZ1 expression and activity are reduced in many cancers. In AML cell lines and patient material, RIZ1 expression is reduced relative to normal bone marrow. In chronic myelogenous leukemia (CML), blastic transformation is associated with loss of heterozygosity in the region where RIZ1 is...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719666/ https://www.ncbi.nlm.nih.gov/pubmed/19602237 http://dx.doi.org/10.1186/1756-8722-2-28 |
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author | Lakshmikuttyamma, Ashakumary Takahashi, Naoto Pastural, Elodie Torlakovic, Emina Amin, Hesham M Garcia-Manero, Guillermo Voralia, Michael Czader, Magdalena DeCoteau, John F Geyer, C Ronald |
author_facet | Lakshmikuttyamma, Ashakumary Takahashi, Naoto Pastural, Elodie Torlakovic, Emina Amin, Hesham M Garcia-Manero, Guillermo Voralia, Michael Czader, Magdalena DeCoteau, John F Geyer, C Ronald |
author_sort | Lakshmikuttyamma, Ashakumary |
collection | PubMed |
description | BACKGROUND: RIZ1 expression and activity are reduced in many cancers. In AML cell lines and patient material, RIZ1 expression is reduced relative to normal bone marrow. In chronic myelogenous leukemia (CML), blastic transformation is associated with loss of heterozygosity in the region where RIZ1 is located. RIZ1 is a PR domain methyltransferase that methylates histone H3 lysine 9, a modification important for transcriptional repression. In CML blast crisis cell lines RIZ1 represses insulin-like growth factor-1 expression and autocrine signaling. Together these observations suggest that RIZ1 may have a role in the chronic phase to blast crisis transition in CML. RESULTS: In CML patient material, we observed that RIZ1 expression was decreased during progression from chronic phase to blast crisis. RIZ1 was expressed in mature myeloid and CD34(+ )cells demonstrating that decreased RIZ1 expression in blast crisis is not due to an increased immature cell population. Expression of RIZ1 CML blast crisis cell lines decreased proliferation, increased apoptosis, and enhanced differentiation. CONCLUSION: RIZ1 is a candidate tumor suppressor gene whose expression is decreased in blast crisis. Loss of RIZ1 activity results in decreased apoptosis and differentiation and enhanced proliferation. Together these results suggest that loss of RIZ1 expression will lead to an increase in myeloid blast cell population resulting in CML progression. |
format | Text |
id | pubmed-2719666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27196662009-08-01 RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression Lakshmikuttyamma, Ashakumary Takahashi, Naoto Pastural, Elodie Torlakovic, Emina Amin, Hesham M Garcia-Manero, Guillermo Voralia, Michael Czader, Magdalena DeCoteau, John F Geyer, C Ronald J Hematol Oncol Short Report BACKGROUND: RIZ1 expression and activity are reduced in many cancers. In AML cell lines and patient material, RIZ1 expression is reduced relative to normal bone marrow. In chronic myelogenous leukemia (CML), blastic transformation is associated with loss of heterozygosity in the region where RIZ1 is located. RIZ1 is a PR domain methyltransferase that methylates histone H3 lysine 9, a modification important for transcriptional repression. In CML blast crisis cell lines RIZ1 represses insulin-like growth factor-1 expression and autocrine signaling. Together these observations suggest that RIZ1 may have a role in the chronic phase to blast crisis transition in CML. RESULTS: In CML patient material, we observed that RIZ1 expression was decreased during progression from chronic phase to blast crisis. RIZ1 was expressed in mature myeloid and CD34(+ )cells demonstrating that decreased RIZ1 expression in blast crisis is not due to an increased immature cell population. Expression of RIZ1 CML blast crisis cell lines decreased proliferation, increased apoptosis, and enhanced differentiation. CONCLUSION: RIZ1 is a candidate tumor suppressor gene whose expression is decreased in blast crisis. Loss of RIZ1 activity results in decreased apoptosis and differentiation and enhanced proliferation. Together these results suggest that loss of RIZ1 expression will lead to an increase in myeloid blast cell population resulting in CML progression. BioMed Central 2009-07-14 /pmc/articles/PMC2719666/ /pubmed/19602237 http://dx.doi.org/10.1186/1756-8722-2-28 Text en Copyright © 2009 Lakshmikuttyamma 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 | Short Report Lakshmikuttyamma, Ashakumary Takahashi, Naoto Pastural, Elodie Torlakovic, Emina Amin, Hesham M Garcia-Manero, Guillermo Voralia, Michael Czader, Magdalena DeCoteau, John F Geyer, C Ronald RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression |
title | RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression |
title_full | RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression |
title_fullStr | RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression |
title_full_unstemmed | RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression |
title_short | RIZ1 is potential CML tumor suppressor that is down-regulated during disease progression |
title_sort | riz1 is potential cml tumor suppressor that is down-regulated during disease progression |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2719666/ https://www.ncbi.nlm.nih.gov/pubmed/19602237 http://dx.doi.org/10.1186/1756-8722-2-28 |
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