GSK-3 inhibitors induce chromosome instability

<p>Abstract</p> <p>Background</p> <p>Several mechanisms operate during mitosis to ensure accurate chromosome segregation. However, during tumour evolution these mechanisms go awry resulting in chromosome instability. While several lines of evidence suggest that mutation...

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Main Authors: Staples Oliver D, Ray-Sinha Arpita, Tighe Anthony, Taylor Stephen S
Format: Article
Language:English
Published: BMC 2007-08-01
Series:BMC Cell Biology
Online Access:http://www.biomedcentral.com/1471-2121/8/34
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spelling doaj-404e43906a23490799d6ec9adf0be0572020-11-25T02:09:25ZengBMCBMC Cell Biology1471-21212007-08-01813410.1186/1471-2121-8-34GSK-3 inhibitors induce chromosome instabilityStaples Oliver DRay-Sinha ArpitaTighe AnthonyTaylor Stephen S<p>Abstract</p> <p>Background</p> <p>Several mechanisms operate during mitosis to ensure accurate chromosome segregation. However, during tumour evolution these mechanisms go awry resulting in chromosome instability. While several lines of evidence suggest that mutations in <it>adenomatous polyposis coli </it>(<it>APC</it>) may promote chromosome instability, at least in colon cancer, the underlying mechanisms remain unclear. Here, we turn our attention to GSK-3 – a protein kinase, which in concert with APC, targets β-catenin for proteolysis – and ask whether GSK-3 is required for accurate chromosome segregation.</p> <p>Results</p> <p>To probe the role of GSK-3 in mitosis, we inhibited GSK-3 kinase activity in cells using a panel of small molecule inhibitors, including SB-415286, AR-A014418, 1-Azakenpaullone and CHIR99021. Analysis of synchronised HeLa cells shows that GSK-3 inhibitors do not prevent G1/S progression or cell division. They do, however, significantly delay mitotic exit, largely because inhibitor-treated cells have difficulty aligning all their chromosomes. Although bipolar spindles form and the majority of chromosomes biorient, one or more chromosomes often remain mono-oriented near the spindle poles. Despite a prolonged mitotic delay, anaphase frequently initiates without the last chromosome aligning, resulting in chromosome non-disjunction. To rule out the possibility of "off-target" effects, we also used RNA interference to selectively repress GSK-3β. Cells deficient for GSK-3β exhibit a similar chromosome alignment defect, with chromosomes clustered near the spindle poles. GSK-3β repression also results in cells accumulating micronuclei, a hallmark of chromosome missegregation.</p> <p>Conclusion</p> <p>Thus, not only do our observations indicate a role for GSK-3 in accurate chromosome segregation, but they also raise the possibility that, if used as therapeutic agents, GSK-3 inhibitors may induce unwanted side effects by inducing chromosome instability.</p> http://www.biomedcentral.com/1471-2121/8/34
collection DOAJ
language English
format Article
sources DOAJ
author Staples Oliver D
Ray-Sinha Arpita
Tighe Anthony
Taylor Stephen S
spellingShingle Staples Oliver D
Ray-Sinha Arpita
Tighe Anthony
Taylor Stephen S
GSK-3 inhibitors induce chromosome instability
BMC Cell Biology
author_facet Staples Oliver D
Ray-Sinha Arpita
Tighe Anthony
Taylor Stephen S
author_sort Staples Oliver D
title GSK-3 inhibitors induce chromosome instability
title_short GSK-3 inhibitors induce chromosome instability
title_full GSK-3 inhibitors induce chromosome instability
title_fullStr GSK-3 inhibitors induce chromosome instability
title_full_unstemmed GSK-3 inhibitors induce chromosome instability
title_sort gsk-3 inhibitors induce chromosome instability
publisher BMC
series BMC Cell Biology
issn 1471-2121
publishDate 2007-08-01
description <p>Abstract</p> <p>Background</p> <p>Several mechanisms operate during mitosis to ensure accurate chromosome segregation. However, during tumour evolution these mechanisms go awry resulting in chromosome instability. While several lines of evidence suggest that mutations in <it>adenomatous polyposis coli </it>(<it>APC</it>) may promote chromosome instability, at least in colon cancer, the underlying mechanisms remain unclear. Here, we turn our attention to GSK-3 – a protein kinase, which in concert with APC, targets β-catenin for proteolysis – and ask whether GSK-3 is required for accurate chromosome segregation.</p> <p>Results</p> <p>To probe the role of GSK-3 in mitosis, we inhibited GSK-3 kinase activity in cells using a panel of small molecule inhibitors, including SB-415286, AR-A014418, 1-Azakenpaullone and CHIR99021. Analysis of synchronised HeLa cells shows that GSK-3 inhibitors do not prevent G1/S progression or cell division. They do, however, significantly delay mitotic exit, largely because inhibitor-treated cells have difficulty aligning all their chromosomes. Although bipolar spindles form and the majority of chromosomes biorient, one or more chromosomes often remain mono-oriented near the spindle poles. Despite a prolonged mitotic delay, anaphase frequently initiates without the last chromosome aligning, resulting in chromosome non-disjunction. To rule out the possibility of "off-target" effects, we also used RNA interference to selectively repress GSK-3β. Cells deficient for GSK-3β exhibit a similar chromosome alignment defect, with chromosomes clustered near the spindle poles. GSK-3β repression also results in cells accumulating micronuclei, a hallmark of chromosome missegregation.</p> <p>Conclusion</p> <p>Thus, not only do our observations indicate a role for GSK-3 in accurate chromosome segregation, but they also raise the possibility that, if used as therapeutic agents, GSK-3 inhibitors may induce unwanted side effects by inducing chromosome instability.</p>
url http://www.biomedcentral.com/1471-2121/8/34
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AT raysinhaarpita gsk3inhibitorsinducechromosomeinstability
AT tigheanthony gsk3inhibitorsinducechromosomeinstability
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