Comparison of Acalabrutinib, A Selective Bruton Tyrosine Kinase Inhibitor, with Ibrutinib in Chronic Lymphocytic Leukemia Cells

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Comparison of Acalabrutinib, A Selective Bruton Tyrosine Kinase Inhibitor, with Ibrutinib in Chronic Lymphocytic Leukemia Cells is …
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scholarly articleQ13442814

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P356DOI10.1158/1078-0432.CCR-16-1446
P932PMC publication ID5491371
P698PubMed publication ID28034907

P50authorWilliam G WierdaQ64026278
Michael J. KeatingQ66429598
Kumudha BalakrishnanQ114427990
Viralkumar PatelQ117256515
P2093author name stringVarsha Gandhi
Mary Ayres
Elena Bibikova
P2860cites workThe Bruton tyrosine kinase inhibitor PCI-32765 blocks B-cell activation and is efficacious in models of autoimmune disease and B-cell malignancyQ24633214
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FDA Approval: Ibrutinib for Patients with Previously Treated Mantle Cell Lymphoma and Previously Treated Chronic Lymphocytic LeukemiaQ33425207
Bruton tyrosine kinase inhibitor ibrutinib (PCI-32765) has significant activity in patients with relapsed/refractory B-cell malignanciesQ33893704
Bruton tyrosine kinase represents a promising therapeutic target for treatment of chronic lymphocytic leukemia and is effectively targeted by PCI-32765.Q34026194
The Bruton tyrosine kinase inhibitor PCI-32765 thwarts chronic lymphocytic leukemia cell survival and tissue homing in vitro and in vivoQ34029869
Ibrutinib versus ofatumumab in previously treated chronic lymphoid leukemiaQ34052075
Primary immunodeficiency diseases due to defects in lymphocytesQ34073630
The clinically active BTK inhibitor PCI-32765 targets B-cell receptor- and chemokine-controlled adhesion and migration in chronic lymphocytic leukemiaQ34249777
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The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinasesQ34355151
Targeting BCL2 with Venetoclax in Relapsed Chronic Lymphocytic LeukemiaQ34504188
Regulation of Mcl-1 expression in context to bone marrow stromal microenvironment in chronic lymphocytic leukemiaQ35022490
Posttranscriptional regulation of Bruton's tyrosine kinase expression in antigen receptor-stimulated splenic B cellsQ35080394
Three-year follow-up of treatment-naïve and previously treated patients with CLL and SLL receiving single-agent ibrutinibQ35450520
Distinct pathways regulate Syk protein activation downstream of immune tyrosine activation motif (ITAM) and hemITAM receptors in plateletsQ35561060
Chronic lymphocytic leukemia: revelations from the B-cell receptor.Q35667038
Etiology of Ibrutinib Therapy Discontinuation and Outcomes in Patients With Chronic Lymphocytic LeukemiaQ35903984
Pharmacological and Protein Profiling Suggests Venetoclax (ABT-199) as Optimal Partner with Ibrutinib in Chronic Lymphocytic LeukemiaQ35958056
The phosphoinositide-3-kinase (PI3K)-delta and gamma inhibitor, IPI-145 (Duvelisib), overcomes signals from the PI3K/AKT/S6 pathway and promotes apoptosis in CLL.Q36021849
Physical and functional association of the Src family kinases Fyn and Lyn with the collagen receptor glycoprotein VI-Fc receptor gamma chain complex on human plateletsQ36401453
Ibrutinib as Initial Therapy for Patients with Chronic Lymphocytic LeukemiaQ36490049
BTK inhibition results in impaired CXCR4 chemokine receptor surface expression, signaling and function in chronic lymphocytic leukemiaQ36799197
Acalabrutinib (ACP-196) in Relapsed Chronic Lymphocytic LeukemiaQ36888218
Ibrutinib is an irreversible molecular inhibitor of ITK driving a Th1-selective pressure in T lymphocytesQ37226729
Lymphocyte cytosolic protein 1 is a chronic lymphocytic leukemia membrane-associated antigen critical to niche homingQ37635605
Targeting Bruton's tyrosine kinase in B cell malignanciesQ38198490
Src family kinases: at the forefront of platelet activationQ38239258
Ibrutinib for patients with relapsed or refractory chronic lymphocytic leukaemia with 17p deletion (RESONATE-17): a phase 2, open-label, multicentre studyQ38956893
Imaging of thrombosis and microcirculation in mouse lungs of initial melanoma metastasis with in vivo cryotechniqueQ39046092
Chronic lymphocytic leukemia B cells express functional CXCR4 chemokine receptors that mediate spontaneous migration beneath bone marrow stromal cells.Q40916348
Unique mutations of Bruton's tyrosine kinase in fourteen unrelated X-linked agammaglobulinemia familiesQ41439621
Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID miceQ41541610
High-level expression of the T-cell chemokines CCL3 and CCL4 by chronic lymphocytic leukemia B cells in nurselike cell cocultures and after BCR stimulationQ42184742
Intracellular Phospho-Flow cytometry reveals novel insights into TCR proximal signaling events. A comparison with Western blotQ44540296
Menaquinone-7 supplementation improves arterial stiffness in healthy postmenopausal women. A double-blind randomised clinical trial.Q53611739
Ibrutinib treatment affects collagen and von Willebrand factor-dependent platelet functions.Q54316160
Ibrutinib inhibits collagen-mediated but not ADP-mediated platelet aggregation.Q54328623
TCR-induced T cell activation leads to simultaneous phosphorylation at Y505 and Y394 of p56(lck) residues.Q54506056
Ibrutinib increases the risk of atrial fibrillation, potentially through inhibition of cardiac PI3K-Akt signaling.Q55069337
Variability in the Degree of Expression of Phosphorylated I B in Chronic Lymphocytic Leukemia Cases With Nodal InvolvementQ58010985
Bruton's Tyrosine Kinase and Phospholipase Cγ2 Mediate Chemokine-Controlled B Cell Migration and HomingQ58324020
Overexpression of the chemokine receptor CXCR4 in B cell chronic lymphocytic leukemia is associated with increased functional response to stromal cell-derived factor-1 (SDF-1)Q73283069
PO-54 - Clinical and laboratory characterization of platelet dysfunction caused by ibrutinib treatment in patients with chronic lymphocytic leukemiaQ89401183
P433issue14
P407language of work or nameEnglishQ1860
P921main subjectchronic lymphocytic leukemiaQ1088156
lymphocyteQ715347
ibrutinibQ5984881
leukemiaQ29496
P304page(s)3734-3743
P577publication date2016-12-29
P1433published inClinical Cancer ResearchQ332253
P1476titleComparison of Acalabrutinib, A Selective Bruton Tyrosine Kinase Inhibitor, with Ibrutinib in Chronic Lymphocytic Leukemia Cells
P478volume23