dc.contributor.author
Smith, Charlotte M.
dc.contributor.author
Haucke, Volker
dc.contributor.author
McCluskey, Adam
dc.contributor.author
Robinson, Phillip J.
dc.contributor.author
Chircop, Megan
dc.date.accessioned
2018-06-08T03:50:50Z
dc.date.available
2014-08-12T09:40:01.105Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/16061
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-20246
dc.description.abstract
Background During metaphase clathrin stabilises the mitotic spindle
kinetochore(K)-fibres. Many anti-mitotic compounds target microtubule
dynamics. Pitstop 2™ is the first small molecule inhibitor of clathrin
terminal domain and inhibits clathrin-mediated endocytosis. We investigated
its effects on a second function for clathrin in mitosis. Results Pitstop 2
did not impair clathrin recruitment to the spindle but disrupted its function
once stationed there. Pitstop 2 trapped HeLa cells in metaphase through loss
of mitotic spindle integrity and activation of the spindle assembly
checkpoint, phenocopying clathrin depletion and aurora A kinase inhibition.
Conclusions Pitstop 2 is therefore a new tool for investigating clathrin
spindle dynamics. Pitstop 2 reduced viability in dividing HeLa cells, without
affecting dividing non-cancerous NIH3T3 cells, suggesting that clathrin is a
possible novel anti-mitotic drug target.
de
dc.rights.uri
http://creativecommons.org/licenses/by/2.0/
dc.subject
Spindle assembly checkpoint
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik
dc.title
Inhibition of clathrin by pitstop 2 activates the spindle assembly checkpoint
and induces cell death in dividing HeLa cancer cells
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Molecular Cancer. - 12 (2013), 1, Artikel Nr. 4/1-15
dc.identifier.sepid
27841
dcterms.bibliographicCitation.doi
10.1186/1476-4598-12-4
dcterms.bibliographicCitation.url
http://dx.doi.org/10.1186/1476-4598-12-4
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.mycore.fudocsId
FUDOCS_document_000000020681
refubium.note.author
Der Artikel wurde in einer Open-Access-Zeitschrift publiziert.
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000003774
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
1476-4598