Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/115401
Title: GRB2 is a BECN1 interacting protein that regulates autophagy
Author(s): Montero-Vergara, Jetsy
Plachetta, Kira
Kinch, Lisa
Bernhardt, StephanLook up in the Integrated Authority File of the German National Library
Kashyap, Kriti
Levine, Beth
Thukral, LipiLook up in the Integrated Authority File of the German National Library
Vetter, MartinaLook up in the Integrated Authority File of the German National Library
Thomssen, ChristophLook up in the Integrated Authority File of the German National Library
Wiemann, StefanLook up in the Integrated Authority File of the German National Library
Peña-Llopis, SamuelLook up in the Integrated Authority File of the German National Library
Jendrossek, VerenaLook up in the Integrated Authority File of the German National Library
Vega-Rubín-de-Celis, SilviaLook up in the Integrated Authority File of the German National Library
Issue Date: 2024
Type: Article
Language: English
Abstract: GRB2 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.
URI: https://opendata.uni-halle.de//handle/1981185920/117355
http://dx.doi.org/10.25673/115401
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Journal Title: Cell death & disease
Publisher: Nature Publishing Group
Publisher Place: London [u.a.]
Volume: 15
Original Publication: 10.1038/s41419-023-06387-7
Page Start: 1
Page End: 11
Appears in Collections:Open Access Publikationen der MLU

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