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Is miR-29 an oncogene or tumor suppressor in CLL?

B-cell chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world. CLL occurs in two forms, aggressive and indolent. Aggressive CLL is characterized by high ZAP-70 expression and unmutated IgH V(H); indolent CLL shows low ZAP-70 expression and mutated IgH V(H). We recently f...

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Detalles Bibliográficos
Autores principales: Pekarsky, Yuri, Croce, Carlo M.
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951328/
https://www.ncbi.nlm.nih.gov/pubmed/20936047
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author Pekarsky, Yuri
Croce, Carlo M.
author_facet Pekarsky, Yuri
Croce, Carlo M.
author_sort Pekarsky, Yuri
collection PubMed
description B-cell chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world. CLL occurs in two forms, aggressive and indolent. Aggressive CLL is characterized by high ZAP-70 expression and unmutated IgH V(H); indolent CLL shows low ZAP-70 expression and mutated IgH V(H). We recently found that miR-29 is upregulated in indolent human B-CLL, compared to aggressive B-CLL and normal CD19+ B-cells. To determine the role of miR-29 in CLL, we generated transgenic mice overexpressing miR-29 in mouse B-cells. Recently we reported that miR-29 transgenic mice develop indolent CLL phenotype. Interestingly, our previous findings suggest that miR-29 targets expression of TCL1, a critical oncogene in aggressive CLL, indicating that miR-29 might function as a tumor suppressor in CLL. Here we discuss these results and provide additional insights into function of miR-29 in CLL.
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spelling pubmed-29513282010-10-07 Is miR-29 an oncogene or tumor suppressor in CLL? Pekarsky, Yuri Croce, Carlo M. Oncotarget Research Perspectives B-cell chronic lymphocytic leukemia (CLL) is the most common leukemia in the Western world. CLL occurs in two forms, aggressive and indolent. Aggressive CLL is characterized by high ZAP-70 expression and unmutated IgH V(H); indolent CLL shows low ZAP-70 expression and mutated IgH V(H). We recently found that miR-29 is upregulated in indolent human B-CLL, compared to aggressive B-CLL and normal CD19+ B-cells. To determine the role of miR-29 in CLL, we generated transgenic mice overexpressing miR-29 in mouse B-cells. Recently we reported that miR-29 transgenic mice develop indolent CLL phenotype. Interestingly, our previous findings suggest that miR-29 targets expression of TCL1, a critical oncogene in aggressive CLL, indicating that miR-29 might function as a tumor suppressor in CLL. Here we discuss these results and provide additional insights into function of miR-29 in CLL. Impact Journals LLC 2010-07-16 /pmc/articles/PMC2951328/ /pubmed/20936047 Text en Copyright: © 2010 Pekarsky and Croce 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 author and source are credited
spellingShingle Research Perspectives
Pekarsky, Yuri
Croce, Carlo M.
Is miR-29 an oncogene or tumor suppressor in CLL?
title Is miR-29 an oncogene or tumor suppressor in CLL?
title_full Is miR-29 an oncogene or tumor suppressor in CLL?
title_fullStr Is miR-29 an oncogene or tumor suppressor in CLL?
title_full_unstemmed Is miR-29 an oncogene or tumor suppressor in CLL?
title_short Is miR-29 an oncogene or tumor suppressor in CLL?
title_sort is mir-29 an oncogene or tumor suppressor in cll?
topic Research Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951328/
https://www.ncbi.nlm.nih.gov/pubmed/20936047
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