Pub. Date : 2019 Dec 4
PMID : 31801949
3 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Resistance to BTK inhibition by ibrutinib can be overcome by preventing FOXO3a nuclear export and PI3K/AKT activation in B-cell lymphoid malignancies. | ibrutinib | AKT serine/threonine kinase 1 | Homo sapiens |
2 | Inhibition of PI3K and AKT using idelalisib and MK2206, respectively increased ibrutinib-induced apoptosis in IB-R cells by downregulation of pAKT473 and restoring FOXO3a levels, demonstrating the importance of these cell survival factors for ibrutinib-resistance. | ibrutinib | AKT serine/threonine kinase 1 | Homo sapiens |
3 | Inhibition of PI3K and AKT using idelalisib and MK2206, respectively increased ibrutinib-induced apoptosis in IB-R cells by downregulation of pAKT473 and restoring FOXO3a levels, demonstrating the importance of these cell survival factors for ibrutinib-resistance. | ibrutinib | AKT serine/threonine kinase 1 | Homo sapiens |