Microenvironment-induced PIM kinases promote CXCR4-triggered mTOR pathway required for chronic lymphocytic leukaemia cell migration
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Microenvironment-induced PIM kinases promote CXCR4-triggered mTOR pathway required for chronic lymphocytic leukaemia cell migration
Authors
Keywords
-
Journal
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
Volume 22, Issue 7, Pages 3548-3559
Publisher
Wiley
Online
2018-04-18
DOI
10.1111/jcmm.13632
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Pim kinase isoforms: devils defending cancer cells from therapeutic and immune attacks
- (2016) Goodwin G. Jinesh et al. APOPTOSIS
- Microenvironment interactions and B-cell receptor signaling in Chronic Lymphocytic Leukemia: Implications for disease pathogenesis and treatment
- (2016) Elisa ten Hacken et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- The BCL2 selective inhibitor venetoclax induces rapid onset apoptosis of CLL cells in patients via a TP53-independent mechanism
- (2016) M. A. Anderson et al. BLOOD
- 4E-BP1, a multifactor regulated multifunctional protein
- (2016) Xiaoyu Qin et al. CELL CYCLE
- Control of translational activation by PIM kinase in activated B-cell diffuse large B-cell lymphoma confers sensitivity to inhibition by PIM447
- (2016) Tara L. Peters et al. Oncotarget
- Prognostic Factors for Chronic Lymphocytic Leukemia
- (2016) Christopher Chen et al. Current Hematologic Malignancy Reports
- FOXO1 activation is an effector of SYK and AKT inhibition in tonic BCR signal-dependent diffuse large B-cell lymphomas
- (2015) M. Szydlowski et al. BLOOD
- Activation of Pim Kinases Is Sufficient to Promote Resistance to MET Small-Molecule Inhibitors
- (2015) N. An et al. CANCER RESEARCH
- BTK inhibition results in impaired CXCR4 chemokine receptor surface expression, signaling and function in chronic lymphocytic leukemia
- (2015) S-S Chen et al. LEUKEMIA
- Increased expression of E3 ubiquitin ligases targeting p53 in CLL patients with wild-type TP53 exhibits associations with clinical features of the disease
- (2015) Patryk Gorniak et al. LEUKEMIA & LYMPHOMA
- Loss of PIM2 enhances the anti-proliferative effect of the pan-PIM kinase inhibitor AZD1208 in non-Hodgkin lymphomas
- (2015) S. Kreuz et al. Molecular Cancer
- PIM kinase (and Akt) biology and signaling in tumors
- (2015) Noel A. Warfel et al. PHARMACOLOGY & THERAPEUTICS
- JAK2 tyrosine kinase mediates integrin activation induced by CXCL12 in B-cell chronic lymphocytic leukemia
- (2015) Alessio Montresor et al. Oncotarget
- Cross-talk between chronic lymphocytic leukemia (CLL) tumor B cells and mesenchymal stromal cells (MSCs): implications for neoplastic cell survival
- (2015) Valentina Trimarco et al. Oncotarget
- Co-culture of primary CLL cells with bone marrow mesenchymal cells, CD40 ligand and CpG ODN promotes proliferation of chemoresistant CLL cells phenotypically comparable to those proliferating in vivo
- (2015) Noelia Purroy et al. Oncotarget
- Stimulation of the B-cell receptor activates the JAK2/STAT3 signaling pathway in chronic lymphocytic leukemia cells
- (2014) U. Rozovski et al. BLOOD
- PIM Kinases Are Essential for Chronic Lymphocytic Leukemia Cell Survival (PIM2/3) and CXCR4-Mediated Microenvironmental Interactions (PIM1)
- (2014) S. Decker et al. MOLECULAR CANCER THERAPEUTICS
- Regulation of Mcl-1 Expression in Context to Bone Marrow Stromal Microenvironment in Chronic Lymphocytic Leukemia
- (2014) Kumudha Balakrishnan et al. NEOPLASIA
- AZD1208, a potent and selective pan-Pim kinase inhibitor, demonstrates efficacy in preclinical models of acute myeloid leukemia
- (2013) E. K. Keeton et al. BLOOD
- Pim2 is required for maintaining multiple myeloma cell growth through modulating TSC2 phosphorylation
- (2013) J. Lu et al. BLOOD
- Chronic lymphocytic leukaemia - the role of the microenvironment pathogenesis and therapy
- (2013) Alan D. Ramsay et al. BRITISH JOURNAL OF HAEMATOLOGY
- “Role of the B-cell receptor and the microenvironment in chronic lymphocytic leukemia’’
- (2013) P Oppezzo et al. Blood Cancer Journal
- Transcription and translation are primary targets of Pim kinase inhibitor SGI-1776 in mantle cell lymphoma
- (2012) Q. Yang et al. BLOOD
- The Pim Kinases: New Targets for Drug Development
- (2011) Ronan Swords et al. CURRENT DRUG TARGETS
- The serine/threonine kinase Pim-2 is a novel anti-apoptotic mediator in myeloma cells
- (2011) J Asano et al. LEUKEMIA
- The lymph node microenvironment promotes B-cell receptor signaling, NF- B activation, and tumor proliferation in chronic lymphocytic leukemia
- (2010) Y. Herishanu et al. BLOOD
- Chronic lymphocytic leukemia cells receive RAF-dependent survival signals in response to CXCL12 that are sensitive to inhibition by sorafenib
- (2010) D. Messmer et al. BLOOD
- PIM1 Protein Kinase regulates PRAS40 phosphorylation and mTOR activity in FDCP1 cells
- (2010) Fengxue Zhang et al. CANCER BIOLOGY & THERAPY
- Pim kinase inhibitor, SGI-1776, induces apoptosis in chronic lymphocytic leukemia cells
- (2009) L. S. Chen et al. BLOOD
- Dissection of PIM serine/threonine kinases in FLT3-ITD–induced leukemogenesis reveals PIM1 as regulator of CXCL12–CXCR4-mediated homing and migration
- (2009) Rebekka Grundler et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Pim-1 plays a pivotal role in hypoxia-induced chemoresistance
- (2009) J Chen et al. ONCOGENE
- Pim Kinases Promote Cell Cycle Progression by Phosphorylating and Down-regulating p27Kip1 at the Transcriptional and Posttranscriptional Levels
- (2008) D. Morishita et al. CANCER RESEARCH
- Multiple signaling pathways promote B lymphocyte stimulator dependent B-cell growth and survival
- (2007) R. T. Woodland et al. BLOOD
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started