
DOI . ORG {
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Title[redir]:
GSI-I (Z-LLNle-CHO) inhibits γ-secretase and the proteosome to trigger cell death in precursor-B acute lymphoblastic leukemia | Leukemia
Description:
Gamma secretase inhibitors (GSIs) comprise a growing class of compounds that interfere with the membrane-bound Notch signaling protein and its downstream intra-nuclear transcriptional targets. As GSI-I (Z-LLNle-CHO) is also a derivative of a widely used proteosome inhibitor MG-132, we hypothesized that this compound might be active in precursor-B acute lymphoblastic leukemia (ALL) cell lines and patient samples. We found that GSI-I treatment of precursor-B ALL blasts induced apoptotic cell death within 18–24 h. With confirmation using RNA and protein analyses, GSI-I blocked nuclear accumulation of cleaved Notch1 and Notch2, and inhibited Notch targets Hey2 and Myc. Microarray analyses of 207 children with high-risk precursor-B ALL demonstrate that Notch pathway expression is a common feature of these neoplasms. However, microarray studies also implicated additional transcriptional targets in GSI-I-dependent cell death, including genes in the unfolded protein response, nuclear factor-κB and p53 pathways. Z-LLNle-CHO blocks both γ-secretase and proteosome activity, inducing more robust cell death in precursor-B ALL cells than either proteosome-selective or γ-secretase-selective inhibitors alone. Using Z-LLNle-CHO in a nonobese diabetes/severe combined immunodeficiency (NOD/SCID) precursor-B ALL xenograft model, we found that GSI-I alone delayed or prevented engraftment of B-lymphoblasts in 50% of the animals comprising the experimental group, suggesting that this compound is worthy of additional testing.
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Keywords {🔍}
notch, cells, gsii, cell, precursorb, article, expression, treatment, google, scholar, cas, figure, usa, leukemia, genes, patients, lines, death, signaling, data, bcell, gene, patient, blood, samples, apoptosis, results, supplementary, acute, proteosome, activity, mice, table, nature, blasts, pathways, group, target, levels, caspase, targets, inhibitor, cancer, show, protein, response, important, analysis, lymphoblastic, normal,
Topics {✒️}
nature portfolio animal research studies onestep rt-pcr kits united blood services nature 2010 nature privacy policy advertising notch-mediated anti-apoptotic pathways pre–pro b-cell state social media present/marginal/absent calls obtained 0/ reprints gsi-i-mediated cell death early b-cell development leukemic b-cell precursors gsi-i-dependent cell death gamma-secretase inhibitors suppress anti-cd19 magnetic beads goat anti-rabbit immunoglobulin standard iacuc-approved techniques z-llnle-cho blocks foxo3 serine/threonine phosphorylation atf4-atf3-chop cascade acute lymphoblastic leukemia nod/scid xenograft model early b-cell malignancies rabbit anti-cd10 antibodies immunoglobulin-β subunit common b-cell commitment factor cryo-preserved bone marrow phosphate-buffered saline-vehicle retinoid-inducible nuclear factor tanoue b-cell line 11 pre-b-cell line mature b-cell neoplasms b-cell development bortezomib-induced cell death notch pathway-related genes author correspondence gamma secretase inhibitor gamma-secretase inhibitor γ-secretase-selective inhibitors pre-b-cell lines t-cell lineage commitment gamma-secretase inhibitors murine xenograft model rt-pcr analysis showed gsi-induced gut toxicity permissions
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headline:GSI-I (Z-LLNle-CHO) inhibits γ-secretase and the proteosome to trigger cell death in precursor-B acute lymphoblastic leukemia
description:Gamma secretase inhibitors (GSIs) comprise a growing class of compounds that interfere with the membrane-bound Notch signaling protein and its downstream intra-nuclear transcriptional targets. As GSI-I (Z-LLNle-CHO) is also a derivative of a widely used proteosome inhibitor MG-132, we hypothesized that this compound might be active in precursor-B acute lymphoblastic leukemia (ALL) cell lines and patient samples. We found that GSI-I treatment of precursor-B ALL blasts induced apoptotic cell death within 18â24âh. With confirmation using RNA and protein analyses, GSI-I blocked nuclear accumulation of cleaved Notch1 and Notch2, and inhibited Notch targets Hey2 and Myc. Microarray analyses of 207 children with high-risk precursor-B ALL demonstrate that Notch pathway expression is a common feature of these neoplasms. However, microarray studies also implicated additional transcriptional targets in GSI-I-dependent cell death, including genes in the unfolded protein response, nuclear factor-κB and p53 pathways. Z-LLNle-CHO blocks both γ-secretase and proteosome activity, inducing more robust cell death in precursor-B ALL cells than either proteosome-selective or γ-secretase-selective inhibitors alone. Using Z-LLNle-CHO in a nonobese diabetes/severe combined immunodeficiency (NOD/SCID) precursor-B ALL xenograft model, we found that GSI-I alone delayed or prevented engraftment of B-lymphoblasts in 50% of the animals comprising the experimental group, suggesting that this compound is worthy of additional testing.
datePublished:2011-04-15T00:00:00Z
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Acute lymphocytic leukaemia
Apoptosis
Mechanism of action
precursor-B acute lymphoblastic leukemia
gamma secretase inhibitor
Notch
proteosome
Medicine/Public Health
general
Internal Medicine
Intensive / Critical Care Medicine
Cancer Research
Oncology
Hematology
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headline:GSI-I (Z-LLNle-CHO) inhibits γ-secretase and the proteosome to trigger cell death in precursor-B acute lymphoblastic leukemia
description:Gamma secretase inhibitors (GSIs) comprise a growing class of compounds that interfere with the membrane-bound Notch signaling protein and its downstream intra-nuclear transcriptional targets. As GSI-I (Z-LLNle-CHO) is also a derivative of a widely used proteosome inhibitor MG-132, we hypothesized that this compound might be active in precursor-B acute lymphoblastic leukemia (ALL) cell lines and patient samples. We found that GSI-I treatment of precursor-B ALL blasts induced apoptotic cell death within 18â24âh. With confirmation using RNA and protein analyses, GSI-I blocked nuclear accumulation of cleaved Notch1 and Notch2, and inhibited Notch targets Hey2 and Myc. Microarray analyses of 207 children with high-risk precursor-B ALL demonstrate that Notch pathway expression is a common feature of these neoplasms. However, microarray studies also implicated additional transcriptional targets in GSI-I-dependent cell death, including genes in the unfolded protein response, nuclear factor-κB and p53 pathways. Z-LLNle-CHO blocks both γ-secretase and proteosome activity, inducing more robust cell death in precursor-B ALL cells than either proteosome-selective or γ-secretase-selective inhibitors alone. Using Z-LLNle-CHO in a nonobese diabetes/severe combined immunodeficiency (NOD/SCID) precursor-B ALL xenograft model, we found that GSI-I alone delayed or prevented engraftment of B-lymphoblasts in 50% of the animals comprising the experimental group, suggesting that this compound is worthy of additional testing.
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Apoptosis
Mechanism of action
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gamma secretase inhibitor
Notch
proteosome
Medicine/Public Health
general
Internal Medicine
Intensive / Critical Care Medicine
Cancer Research
Oncology
Hematology
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address:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:R C Harvey
affiliation:
name:University of New Mexico Health Sciences Center
address:
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:The UNM Cancer Center, University of New Mexico Health Sciences Center
address:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:S P Hunger
affiliation:
name:The Children's Hospital and the University of Colorado Denver School of Medicine
address:
name:Department of Pediatrics, The Children's Hospital and the University of Colorado Denver School of Medicine, Aurora, USA
type:PostalAddress
type:Organization
name:S A Ness
affiliation:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center
address:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:University of New Mexico Health Sciences Center
address:
name:Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:S S Winter
affiliation:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center
address:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:University of New Mexico Health Sciences Center
address:
name:Department of Pediatrics, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
email:[email protected]
name:B S Wilson
affiliation:
name:University of New Mexico Health Sciences Center
address:
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
name:The UNM Cancer Center, University of New Mexico Health Sciences Center
address:
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
type:PostalAddress
type:Organization
PostalAddress:
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:8Current address: Department of Obstetrics and Gynecology, University of Iowa, Iowa City, IA 52242, USA.,
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Laboratoire dâHématologie, Centre Hospitalier Universitaire de Dijon, Dijon, France
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Physics, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pediatrics, The Children's Hospital and the University of Colorado Denver School of Medicine, Aurora, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Molecular Genetics and Microbiology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pediatrics, University of New Mexico Health Sciences Center, Albuquerque, USA
name:Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque, USA
name:The UNM Cancer Center, University of New Mexico Health Sciences Center, Albuquerque, USA
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