Protein kinase C alpha-mediated phosphorylation of PIM-1L promotes the survival and proliferation of acute myeloid leukemia cells

2018 ◽  
Vol 503 (3) ◽  
pp. 1364-1371 ◽  
Author(s):  
Mayu Takami ◽  
Kazuhiro Katayama ◽  
Kohji Noguchi ◽  
Yoshikazu Sugimoto
Oncogene ◽  
2020 ◽  
Vol 39 (19) ◽  
pp. 3910-3925
Author(s):  
Muskan Floren ◽  
Sebastian Restrepo Cruz ◽  
Christina M. Termini ◽  
Kristopher D. Marjon ◽  
Keith A. Lidke ◽  
...  

Blood ◽  
1993 ◽  
Vol 82 (10) ◽  
pp. 3133-3140 ◽  
Author(s):  
K Bhalla ◽  
AM Ibrado ◽  
E Tourkina ◽  
C Tang ◽  
S Grant ◽  
...  

Abstract Mitoxantrone has been shown in vitro to exhibit a steep dose-response relationship with respect to the clonogenic survival of acute myeloid leukemia cells. In this report, we show that 1-hour exposure of human myeloid leukemia HL-60 and KG-1 cells to mitoxantrone concentrations ranging between 0.1 and 10.0 mumol/L induced internucleosomal DNA fragmentation of approximately 200-bp integer multiples, characteristic of cells undergoing programmed cell death (PCD) or apoptosis. Mitoxantrone-mediated PCD was associated with a steep inhibition of the clonogenic survival of the leukemic cells. In addition, intracellularly, mitoxantrone-induced PCD was associated with a marked induction of c-jun and significant repression of c-myc and BCL-2 oncogenes. Pretreatment with the protein kinase C stimulator phorbol myristate acetate enhanced mitoxantrone-induced internucleosomal DNA fragmentation, whereas protein kinase C inhibitors staurosporine and H7 had no effect. These findings suggest that PCD is a potential mechanism underlying the steep dose-response relationship of mitoxantrone to the inhibition of clonogenic survival of acute myeloid leukemia cells.


2020 ◽  
Vol 13 (7) ◽  
pp. 100780
Author(s):  
Peter M. Alexander ◽  
Gregory L. Kucera ◽  
Kristin M. Pladna ◽  
Timothy S. Pardee

Blood ◽  
1993 ◽  
Vol 82 (10) ◽  
pp. 3133-3140 ◽  
Author(s):  
K Bhalla ◽  
AM Ibrado ◽  
E Tourkina ◽  
C Tang ◽  
S Grant ◽  
...  

Mitoxantrone has been shown in vitro to exhibit a steep dose-response relationship with respect to the clonogenic survival of acute myeloid leukemia cells. In this report, we show that 1-hour exposure of human myeloid leukemia HL-60 and KG-1 cells to mitoxantrone concentrations ranging between 0.1 and 10.0 mumol/L induced internucleosomal DNA fragmentation of approximately 200-bp integer multiples, characteristic of cells undergoing programmed cell death (PCD) or apoptosis. Mitoxantrone-mediated PCD was associated with a steep inhibition of the clonogenic survival of the leukemic cells. In addition, intracellularly, mitoxantrone-induced PCD was associated with a marked induction of c-jun and significant repression of c-myc and BCL-2 oncogenes. Pretreatment with the protein kinase C stimulator phorbol myristate acetate enhanced mitoxantrone-induced internucleosomal DNA fragmentation, whereas protein kinase C inhibitors staurosporine and H7 had no effect. These findings suggest that PCD is a potential mechanism underlying the steep dose-response relationship of mitoxantrone to the inhibition of clonogenic survival of acute myeloid leukemia cells.


2017 ◽  
Vol 24 (3) ◽  
pp. 608-618 ◽  
Author(s):  
Daniela Di Marcantonio ◽  
Esteban Martinez ◽  
Simone Sidoli ◽  
Jessica Vadaketh ◽  
Margaret Nieborowska-Skorska ◽  
...  

Blood ◽  
2005 ◽  
Vol 106 (4) ◽  
pp. 1362-1368 ◽  
Author(s):  
Peter Hampson ◽  
Hema Chahal ◽  
Farhat Khanim ◽  
Rachel Hayden ◽  
Anneke Mulder ◽  
...  

Abstract Ingenol 3-angelate (PEP005) is a selective small molecule activator of protein kinase C (PKC) extracted from the plant Euphorbia peplus, whose sap has been used as a traditional medicine for the treatment of skin conditions including warts and cancer. We report here that PEP005 also has potent antileukemic effects, inducing apoptosis in myeloid leukemia cell lines and primary acute myeloid leukemia (AML) cells at nanomolar concentrations. Of importance, PEP005 did not induce apoptosis in normal CD34+ cord blood myeloblasts at up to 2-log concentrations higher than those required to induce cell death in primary AML cells. The effects of PEP005 were PKC dependent, and PEP005 efficacy correlated with expression of PKC-delta. The delta isoform of PKC plays a key role in apoptosis and is therefore a rational potential target for antileukemic therapies. Transfection of KG1a leukemia cells, which did not express PKC-delta or respond to PEP005, with enhanced green fluorescent protein (EGFP)-PKC-delta restored sensitivity to induction of apoptosis by PEP005. Our data therefore suggest that activation of PKC-delta provides a novel approach for treatment of acute myeloid leukemia and that screening for PKC-delta expression may identify patients for potential responsiveness to PEP005. (Blood. 2005;106:1362-1368)


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