dc.contributor.author | Gurden, MD | |
dc.contributor.author | Anderhub, SJ | |
dc.contributor.author | Faisal, A | |
dc.contributor.author | Linardopoulos, S | |
dc.date.accessioned | 2016-09-05T11:53:39Z | |
dc.date.issued | 2018-04-13 | |
dc.identifier.citation | Oncotarget, 2016 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/95 | |
dc.identifier.eissn | 1949-2553 | |
dc.identifier.doi | 10.18632/oncotarget.10657 | |
dc.description.abstract | Accurate chromosome segregation is dependent on the spindle assembly checkpoint (SAC). In current models, the key direct role of Aurora B in the SAC has been suggested to be to promote rapid kinetochore localisation of MPS1, allowing MPS1 to generate the checkpoint signal. However, Aurora B is also thought to play an indirect role in the SAC through the destabilisation of kinetochore-microtubule (KT-MT) attachments. Here, we demonstrate that Aurora B activity is not required for the kinetochore recruitment of the majority of SAC proteins. More importantly, we show that the primary role of Aurora B in the SAC is to prevent the premature removal of SAC proteins from the kinetochore, which is strictly dependent on KT-MT interactions. Moreover, in the presence of KT-MT interactions, Aurora B inhibition silences a persistent SAC induced by tethering MPS1 to the kinetochore. This explains the highly synergistic interaction between Aurora B and MPS1 inhibitors to override the SAC, which is lost when cells are pre-arrested in nocodazole. Furthermore, we show that Aurora B and MPS1 inhibitors synergistically kill a panel of breast and colon cancer cell lines, including cells that are otherwise insensitive to Aurora B inhibitors alone. These data demonstrate that the major role of Aurora B in SAC is to prevent the removal of SAC proteins from tensionless kinetochores, thus inhibiting premature SAC silencing, and highlights a therapeutic strategy through combination of Aurora B and MPS1 inhibitors. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | Impact Journals, LLC | |
dc.relation.isreplacedby | internal/4151 | |
dc.relation.isreplacedby | https://repository.icr.ac.uk/handle/internal/4151 | |
dc.relation.isreplacedby | internal/4151 | |
dc.relation.isreplacedby | https://repository.icr.ac.uk/handle/internal/4151 | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | |
dc.title | Aurora B prevents premature removal of spindle assembly checkpoint proteins from the kinetochore: A key role for Aurora B in mitosis. | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2016-06-01 | |
rioxxterms.versionofrecord | 10.18632/oncotarget.10657 | |
rioxxterms.licenseref.uri | https://creativecommons.org/licenses/by/4.0 | |
rioxxterms.licenseref.startdate | 2016-07-18 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | Oncotarget | |
pubs.declined | 2016-08-31T15:07:56.305+0100 | |
pubs.declined | 2016-08-31T15:07:56.305+0100 | |
pubs.deleted | 2016-08-31T15:07:56.305+0100 | |
pubs.merge-to | internal/4151 | |
pubs.merge-to | https://repository.icr.ac.uk/handle/internal/4151 | |
pubs.notes | Not known | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Drug Target Discovery | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Breast Cancer Research/Drug Target Discovery | |
pubs.embargo.terms | Not known | |
icr.researchteam | Drug Target Discovery | |
dc.contributor.icrauthor | Linardopoulos, Spyridon | |