BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.

BCL2 associated Athano-Gene 1 (BAG1) is a multifunctional protein that has been described to be involved in different cell processes linked to cell survival. It has been reported as deregulated in diverse cancer types. Here, BAG1 protein was found highly expressed in children with acute myeloid leuk...

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Main Authors: Sanja Aveic, Martina Pigazzi, Giuseppe Basso
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3189928?pdf=render
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spelling doaj-fb043f5cd3b54d2c907a8748d8ac85752020-11-25T01:19:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2609710.1371/journal.pone.0026097BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.Sanja AveicMartina PigazziGiuseppe BassoBCL2 associated Athano-Gene 1 (BAG1) is a multifunctional protein that has been described to be involved in different cell processes linked to cell survival. It has been reported as deregulated in diverse cancer types. Here, BAG1 protein was found highly expressed in children with acute myeloid leukemia at diagnosis, and in a cohort of leukemic cell lines. A silencing approach was used for determining BAG1's role in AML, finding that its down-regulation decreased expression of BCL2, BCL-XL, MCL1, and phospho-ERK1/2, all proteins able to sustain leukemia, without affecting the pro-apoptotic protein BAX. BAG1 down-regulation was also found to increase expression of BAG3, whose similar activity was able to compensate the loss of function of BAG1. BAG1/BAG3 co-silencing caused an enhanced cell predisposition to death in cell lines and also in primary AML cultures, affecting the same proteins. Cell death was CASPASE-3 dependent, was accompanied by PARP cleavage and documented by an increased release of pro-apoptotic molecules Smac/DIABLO and Cytochrome c. BAG1 was found to directly maintain BCL2 and to protect MCL1 from proteasomal degradation by controlling USP9X expression, which appeared to be its novel target. Finally, BAG1 was found able to affect leukemia cell fate by influencing the expression of anti-apoptotic proteins crucial for AML maintenance.http://europepmc.org/articles/PMC3189928?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sanja Aveic
Martina Pigazzi
Giuseppe Basso
spellingShingle Sanja Aveic
Martina Pigazzi
Giuseppe Basso
BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
PLoS ONE
author_facet Sanja Aveic
Martina Pigazzi
Giuseppe Basso
author_sort Sanja Aveic
title BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
title_short BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
title_full BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
title_fullStr BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
title_full_unstemmed BAG1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
title_sort bag1: the guardian of anti-apoptotic proteins in acute myeloid leukemia.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description BCL2 associated Athano-Gene 1 (BAG1) is a multifunctional protein that has been described to be involved in different cell processes linked to cell survival. It has been reported as deregulated in diverse cancer types. Here, BAG1 protein was found highly expressed in children with acute myeloid leukemia at diagnosis, and in a cohort of leukemic cell lines. A silencing approach was used for determining BAG1's role in AML, finding that its down-regulation decreased expression of BCL2, BCL-XL, MCL1, and phospho-ERK1/2, all proteins able to sustain leukemia, without affecting the pro-apoptotic protein BAX. BAG1 down-regulation was also found to increase expression of BAG3, whose similar activity was able to compensate the loss of function of BAG1. BAG1/BAG3 co-silencing caused an enhanced cell predisposition to death in cell lines and also in primary AML cultures, affecting the same proteins. Cell death was CASPASE-3 dependent, was accompanied by PARP cleavage and documented by an increased release of pro-apoptotic molecules Smac/DIABLO and Cytochrome c. BAG1 was found to directly maintain BCL2 and to protect MCL1 from proteasomal degradation by controlling USP9X expression, which appeared to be its novel target. Finally, BAG1 was found able to affect leukemia cell fate by influencing the expression of anti-apoptotic proteins crucial for AML maintenance.
url http://europepmc.org/articles/PMC3189928?pdf=render
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