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Lessons Learned: HIV Points the Way Towards Precision Treatment of Mixed-Lineage Leukemia
K. Cermakova, C. Weydert, F. Christ, J. De Rijck, Z. Debyser,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, přehledy, práce podpořená grantem
- MeSH
- adaptorové proteiny signální transdukční genetika metabolismus MeSH
- cílená molekulární terapie MeSH
- histonlysin-N-methyltransferasa genetika metabolismus MeSH
- HIV infekce farmakoterapie genetika metabolismus MeSH
- individualizovaná medicína metody MeSH
- interakční proteinové domény a motivy MeSH
- knihovny malých molekul farmakologie MeSH
- kontraindikace MeSH
- leukemie farmakoterapie genetika metabolismus MeSH
- lidé MeSH
- molekulární modely MeSH
- protoonkogenní protein MLL genetika metabolismus MeSH
- transkripční faktory genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
Protein-protein interactions are involved in most if not all pathogenic and pathophysiological processes and represent attractive therapeutic targets. Extensive biological and clinical research efforts have led to the identification and validation of several cellular hubs that are crucially involved in disease pathogenesis. An interesting example of such a hub is the lens epithelium-derived growth factor (LEDGF/p75), a protein that tethers multiple unrelated proteins and protein complexes to the chromatin. Its chromatin-tethering ability is linked to at least two unrelated diseases-HIV infection and MLL-rearranged acute leukemia. In this review we discuss recent progress in our understanding of the interaction of LEDGF/p75 with its binding partners and focus on the first steps towards therapies targeting protein-protein interactions of LEDGF/p75.
Citace poskytuje Crossref.org
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