Cargando…
Max deletion destabilizes MYC protein and abrogates Eµ-Myc lymphomagenesis
Although MAX is regarded as an obligate dimerization partner for MYC, its function in normal development and neoplasia is poorly defined. We show that B-cell-specific deletion of Max has a modest effect on B-cell development but completely abrogates Eµ-Myc-driven lymphomagenesis. While Max loss affe...
Autores principales: | Mathsyaraja, Haritha, Freie, Brian, Cheng, Pei-Feng, Babaeva, Ekaterina, Catchpole, Jonathen T., Janssens, Derek, Henikoff, Steven, Eisenman, Robert N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719623/ https://www.ncbi.nlm.nih.gov/pubmed/31395740 http://dx.doi.org/10.1101/gad.325878.119 |
Ejemplares similares
-
The MYC transcription factor network: balancing metabolism, proliferation and oncogenesis
por: Carroll, Patrick A., et al.
Publicado: (2018) -
Anti-apoptotic A1 is not essential for lymphoma development in Eµ-Myc mice but helps sustain transplanted Eµ-Myc tumour cells
por: Mensink, Mark, et al.
Publicado: (2018) -
Mnt modulates Myc-driven lymphomagenesis
por: Campbell, Kirsteen J, et al.
Publicado: (2017) -
Role of MYC in B Cell Lymphomagenesis
por: Korać, Petra, et al.
Publicado: (2017) -
Deletion of the transcriptional regulator TFAP4 accelerates c-MYC-driven lymphomagenesis
por: Potts, Margaret A., et al.
Publicado: (2023)