Search Results - "Schneider, Paula A."
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1
Transient binding of an activator BH3 domain to the Bak BH3-binding groove initiates Bak oligomerization
Published in The Journal of cell biology (11-07-2011)“…The mechanism by which the proapoptotic Bcl-2 family members Bax and Bak release cytochrome c from mitochondria is incompletely understood. In this paper, we…”
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2
A phase I study of pevonedistat, azacitidine, and venetoclax in patients with relapsed/refractory acute myeloid leukemia
Published in Haematologica (Roma) (01-09-2024)“…Azacitidine/venetoclax is an active regimen in patients with newly diagnosed acute myeloid leukemia (AML). However, primary or secondary resistance to…”
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3
Fatty acid synthase (FASN) regulates the mitochondrial priming of cancer cells
Published in Cell death & disease (21-10-2021)“…Inhibitors of the lipogenic enzyme fatty acid synthase (FASN) have attracted much attention in the last decade as potential targeted cancer therapies. However,…”
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4
Immunodetection of human topoisomerase I-DNA covalent complexes
Published in Nucleic acids research (07-04-2016)“…A number of established and investigational anticancer drugs slow the religation step of DNA topoisomerase I (topo I). These agents induce cytotoxicity by…”
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5
Constitutive BAK activation as a determinant of drug sensitivity in malignant lymphohematopoietic cells
Published in Genes & development (15-10-2015)“…Mitochondrial outer membrane permeabilization (MOMP), a key step in the intrinsic apoptotic pathway, is incompletely understood. Current models emphasize the…”
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6
Enhanced Killing of Cancer Cells by Poly(ADP-ribose) Polymerase Inhibitors and Topoisomerase I Inhibitors Reflects Poisoning of Both Enzymes
Published in The Journal of biological chemistry (03-02-2012)“…Poly(ADP-ribose) polymerase-1 (PARP1) plays critical roles in the regulation of DNA repair. Accordingly, small molecule inhibitors of PARP are being developed…”
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7
Proapoptotic activity of JNK-sensitive BH3-only proteins underpins ovarian cancer response to replication checkpoint inhibitors
Published in Molecular cancer (07-10-2024)“…Recent studies indicate that replication checkpoint modulators (RCMs) such as inhibitors of CHK1, ATR, and WEE1 have promising monotherapy activity in solid…”
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8
Relationship between BCL2 mutations and follicular lymphoma outcome in the chemoimmunotherapy era
Published in Blood cancer journal (New York) (17-05-2023)“…How to identify follicular lymphoma (FL) patients with low disease burden but high risk for early progression is unclear. Building on a prior study…”
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Dual mTORC1/mTORC2 inhibition diminishes Akt activation and induces Puma-dependent apoptosis in lymphoid malignancies
Published in Blood (12-01-2012)“…The mammalian target of rapamycin (mTOR) plays crucial roles in proliferative and antiapoptotic signaling in lymphoid malignancies. Rapamycin analogs, which…”
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10
A phase 2 and pharmacological study of sapanisertib in patients with relapsed and/or refractory acute lymphoblastic leukemia
Published in Cancer medicine (Malden, MA) (01-12-2023)“…Background Despite recent approval of several new agents, relapsed acute lymphoblastic leukemia (ALL) remains challenging to treat. Sapanisertib…”
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11
Context-dependent Bcl-2/Bak Interactions Regulate Lymphoid Cell Apoptosis
Published in The Journal of biological chemistry (03-07-2009)“…The release of cytochrome c from mitochondria, which leads to activation of the intrinsic apoptotic pathway, is regulated by interactions of Bax and Bak with…”
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12
Cytotoxicity of farnesyltransferase inhibitors in lymphoid cells mediated by MAPK pathway inhibition and Bim up-regulation
Published in Blood (03-11-2011)“…The mechanism of cytotoxicity of farnesyltransferase inhibitors is incompletely understood and seems to vary depending on the cell type. To identify potential…”
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13
Contribution of Bcl-2 Phosphorylation to Bak Binding and Drug Resistance
Published in Cancer research (Chicago, Ill.) (01-12-2013)“…Bcl-2 is phosphorylated on Ser(70) after treatment of cells with spindle poisons. On the basis of effects observed in cells overexpressing Bcl-2 S70E or S70A…”
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14
BCL2 mutations are associated with increased risk of transformation and shortened survival in follicular lymphoma
Published in Blood (22-01-2015)“…Follicular lymphoma (FL), an indolent neoplasm caused by a t(14;18) chromosomal translocation that juxtaposes the BCL2 gene and immunoglobulin locus, has a…”
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15
Farnesyltransferase inhibitor tipifarnib inhibits Rheb prenylation and stabilizes Bax in acute myelogenous leukemia cells
Published in Haematologica (Roma) (01-01-2014)“…Although farnesyltransferase inhibitors have shown promising activity in relapsed lymphoma and sporadic activity in acute myelogenous leukemia, their mechanism…”
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16
AMPK inhibition sensitizes acute leukemia cells to BH3 mimetic-induced cell death
Published in Cell death and differentiation (01-04-2024)“…BH3 mimetics, including the BCL2/BCLX L /BCLw inhibitor navitoclax and MCL1 inhibitors S64315 and tapotoclax, have undergone clinical testing for a variety of…”
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17
Measurement of BH3-only protein tolerance
Published in Cell death and differentiation (01-02-2018)“…The BCL2 family of proteins regulates cellular life and death decisions. Among BCL2 family members, BH3-only proteins have critical roles by neutralizing…”
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18
Poly(ADP-ribose) Polymerase Inhibitors Sensitize Cancer Cells to Death Receptor-mediated Apoptosis by Enhancing Death Receptor Expression
Published in The Journal of biological chemistry (25-07-2014)“…Recombinant human tumor necrosis factor-α-related apoptosis inducing ligand (TRAIL), agonistic monoclonal antibodies to TRAIL receptors, and small molecule…”
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19
4EBP1/c-MYC/PUMA and NF-κB/EGR1/BIM pathways underlie cytotoxicity of mTOR dual inhibitors in malignant lymphoid cells
Published in Blood (02-06-2016)“…The mammalian target of rapamycin (mTOR), a kinase that regulates proliferation and apoptosis, has been extensively evaluated as a therapeutic target in…”
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20
CDK2-Mediated Upregulation of TNFα as a Mechanism of Selective Cytotoxicity in Acute Leukemia
Published in Cancer research (Chicago, Ill.) (15-05-2021)“…Although inhibitors of the kinases CHK1, ATR, and WEE1 are undergoing clinical testing, it remains unclear how these three classes of agents kill susceptible…”
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