Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/115401
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dc.contributor.authorMontero-Vergara, Jetsy-
dc.contributor.authorPlachetta, Kira-
dc.contributor.authorKinch, Lisa-
dc.contributor.authorBernhardt, Stephan-
dc.contributor.authorKashyap, Kriti-
dc.contributor.authorLevine, Beth-
dc.contributor.authorThukral, Lipi-
dc.contributor.authorVetter, Martina-
dc.contributor.authorThomssen, Christoph-
dc.contributor.authorWiemann, Stefan-
dc.contributor.authorPeña-Llopis, Samuel-
dc.contributor.authorJendrossek, Verena-
dc.contributor.authorVega-Rubín-de-Celis, Silvia-
dc.date.accessioned2024-03-19T12:08:28Z-
dc.date.available2024-03-19T12:08:28Z-
dc.date.issued2024-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/117355-
dc.identifier.urihttp://dx.doi.org/10.25673/115401-
dc.description.abstractGRB2 is an adaptor protein of HER2 (and several other tyrosine kinases), which we identified as a novel BECN1 (Beclin 1) interacting partner. GRB2 co-immunoprecipitated with BECN1 in several breast cancer cell lines and regulates autophagy through a mechanism involving the modulation of the class III PI3Kinase VPS34 activity. In ovo studies in a CAM (Chicken Chorioallantoic Membrane) model indicated that GRB2 knockdown, as well as overexpression of GRB2 loss-of-function mutants (Y52A and S86A-R88A) compromised tumor growth. These differences in tumor growth correlated with differential autophagy activity, indicating that autophagy effects might be related to the effects on tumorigenesis. Our data highlight a novel function of GRB2 as a BECN1 binding protein and a regulator of autophagy.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc610-
dc.titleGRB2 is a BECN1 interacting protein that regulates autophagyeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleCell death & disease-
local.bibliographicCitation.volume15-
local.bibliographicCitation.pagestart1-
local.bibliographicCitation.pageend11-
local.bibliographicCitation.publishernameNature Publishing Group-
local.bibliographicCitation.publisherplaceLondon [u.a.]-
local.bibliographicCitation.doi10.1038/s41419-023-06387-7-
local.openaccesstrue-
dc.identifier.ppn1883789885-
cbs.publication.displayform2024-
local.bibliographicCitation.year2024-
cbs.sru.importDate2024-03-19T12:08:03Z-
local.bibliographicCitationEnthalten in Cell death & disease - London [u.a.] : Nature Publishing Group, 2010-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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