Notch Signaling Promotes Mature T-Cell Lymphomagenesis

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Peripheral T-cell lymphomas (PTCL) are agressive lymphomas engineered mouse models and spontaneous PTCL models were that develop from mature T cells. The most common PTCLs are used to functionally examine the role of Notch signaling, and genetically, molecularly, and clinically diverse and are gener...

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Autores: Gao, X, Wang, C, Abdelrahman, S, Kady, N, Murga-Zamalloa, C, Gann, P, Sverdlov, M, Wolfe, A, Polk, A, Brown, N, Bailey, N, Inamdar, K, Casavilca-Zambrano, S, Montes Gil, J, Barrionuevo, C, Taxa-Rojas, L, Reneau, J, Siebe, CW, Maillard, I, Wilcox, RA
Formato: artículo
Fecha de Publicación:2022
Institución:Instituto Nacional de Enfermedades Neoplásicas
Repositorio:INEN-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.inen.sld.pe:20.500.14703/260
Enlace del recurso:https://hdl.handle.net/20.500.14703/260
Nivel de acceso:acceso abierto
Materia:T-Cell Lymphomagenesis
https://purl.org/pe-repo/ocde/ford#3.02.21
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spelling PublicationGao, XWang, CAbdelrahman, SKady, NMurga-Zamalloa, CGann, PSverdlov, MWolfe, APolk, ABrown, NBailey, NInamdar, KCasavilca-Zambrano, SMontes Gil, JBarrionuevo, CTaxa-Rojas, LReneau, JSiebe, CWMaillard, IWilcox, RA2025-01-02T14:42:02Z2025-01-02T14:42:02Z202210.1158/0008-5472.CAN-22-1215https://hdl.handle.net/20.500.14703/260Cancer ResearchPeripheral T-cell lymphomas (PTCL) are agressive lymphomas engineered mouse models and spontaneous PTCL models were that develop from mature T cells. The most common PTCLs are used to functionally examine the role of Notch signaling, and genetically, molecularly, and clinically diverse and are generally Notch1/Notch2 blockade and pan-Notch blockade using domiassociated with dismal outcomes. While Notch signaling plays a nant-negative MAML significantly impaired the proliferation of critically important role in both the development of immature T malignant T cells and PTCL progression in these models. Treatment cells and their malignant transformation, its role in PTCL is poorly with DLL1/DLL4 blocking antibodies established that Notch sigunderstood, despite the increasingly appreciated function of Notch naling is ligand-dependent. Together, these findings reveal a role for in regulating the proliferation and differentiation of mature T cells. ligand-dependent Notch signaling in driving peripheral T-cell Here, we demonstrate that Notch receptors and their Delta-like lymphomagenesis. family ligands (DLL1/DLL4) play a pathogenic role in PTCL. Notch1 activation was observed in common PTCL subtypes, includSignificance: This work demonstrates that ligand-dependent ing PTCL-not otherwise specified (NOS). In a large cohort of PTCL-Notch activation promotes the growth and proliferation of mature NOS biopsies, Notch1 activation was significantly associated with T-cell lymphomas, providing new therapeutic strategies for this surrogate markers of proliferation. Complementary genetically group of aggressive lymphomas. 2022 American Association for Cancer Research.application/pdfengAmerican Association for Cancer Research Inc.USinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/4.0/T-Cell Lymphomagenesishttps://purl.org/pe-repo/ocde/ford#3.02.21Notch Signaling Promotes Mature T-Cell Lymphomagenesisinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:INEN-Institucionalinstname:Instituto Nacional de Enfermedades Neoplásicasinstacron:INEN20.500.14703/260oai:repositorio.inen.sld.pe:20.500.14703/2602026-02-17T14:35:24.402Zhttps://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessmetadata.onlyhttps://repositorio.inen.sld.peRepositorio del Instituto Nacional de Enfermedades Neoplásicasrepositorio@inen.sld.pe
dc.title.none.fl_str_mv Notch Signaling Promotes Mature T-Cell Lymphomagenesis
title Notch Signaling Promotes Mature T-Cell Lymphomagenesis
spellingShingle Notch Signaling Promotes Mature T-Cell Lymphomagenesis
Gao, X
T-Cell Lymphomagenesis
https://purl.org/pe-repo/ocde/ford#3.02.21
title_short Notch Signaling Promotes Mature T-Cell Lymphomagenesis
title_full Notch Signaling Promotes Mature T-Cell Lymphomagenesis
title_fullStr Notch Signaling Promotes Mature T-Cell Lymphomagenesis
title_full_unstemmed Notch Signaling Promotes Mature T-Cell Lymphomagenesis
title_sort Notch Signaling Promotes Mature T-Cell Lymphomagenesis
author Gao, X
author_facet Gao, X
Wang, C
Abdelrahman, S
Kady, N
Murga-Zamalloa, C
Gann, P
Sverdlov, M
Wolfe, A
Polk, A
Brown, N
Bailey, N
Inamdar, K
Casavilca-Zambrano, S
Montes Gil, J
Barrionuevo, C
Taxa-Rojas, L
Reneau, J
Siebe, CW
Maillard, I
Wilcox, RA
author_role author
author2 Wang, C
Abdelrahman, S
Kady, N
Murga-Zamalloa, C
Gann, P
Sverdlov, M
Wolfe, A
Polk, A
Brown, N
Bailey, N
Inamdar, K
Casavilca-Zambrano, S
Montes Gil, J
Barrionuevo, C
Taxa-Rojas, L
Reneau, J
Siebe, CW
Maillard, I
Wilcox, RA
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Gao, X
Wang, C
Abdelrahman, S
Kady, N
Murga-Zamalloa, C
Gann, P
Sverdlov, M
Wolfe, A
Polk, A
Brown, N
Bailey, N
Inamdar, K
Casavilca-Zambrano, S
Montes Gil, J
Barrionuevo, C
Taxa-Rojas, L
Reneau, J
Siebe, CW
Maillard, I
Wilcox, RA
dc.subject.none.fl_str_mv T-Cell Lymphomagenesis
topic T-Cell Lymphomagenesis
https://purl.org/pe-repo/ocde/ford#3.02.21
dc.subject.ocde.none.fl_str_mv https://purl.org/pe-repo/ocde/ford#3.02.21
description Peripheral T-cell lymphomas (PTCL) are agressive lymphomas engineered mouse models and spontaneous PTCL models were that develop from mature T cells. The most common PTCLs are used to functionally examine the role of Notch signaling, and genetically, molecularly, and clinically diverse and are generally Notch1/Notch2 blockade and pan-Notch blockade using domiassociated with dismal outcomes. While Notch signaling plays a nant-negative MAML significantly impaired the proliferation of critically important role in both the development of immature T malignant T cells and PTCL progression in these models. Treatment cells and their malignant transformation, its role in PTCL is poorly with DLL1/DLL4 blocking antibodies established that Notch sigunderstood, despite the increasingly appreciated function of Notch naling is ligand-dependent. Together, these findings reveal a role for in regulating the proliferation and differentiation of mature T cells. ligand-dependent Notch signaling in driving peripheral T-cell Here, we demonstrate that Notch receptors and their Delta-like lymphomagenesis. family ligands (DLL1/DLL4) play a pathogenic role in PTCL. Notch1 activation was observed in common PTCL subtypes, includSignificance: This work demonstrates that ligand-dependent ing PTCL-not otherwise specified (NOS). In a large cohort of PTCL-Notch activation promotes the growth and proliferation of mature NOS biopsies, Notch1 activation was significantly associated with T-cell lymphomas, providing new therapeutic strategies for this surrogate markers of proliferation. Complementary genetically group of aggressive lymphomas. 2022 American Association for Cancer Research.
publishDate 2022
dc.date.accessioned.none.fl_str_mv 2025-01-02T14:42:02Z
dc.date.available.none.fl_str_mv 2025-01-02T14:42:02Z
dc.date.issued.fl_str_mv 2022
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.doi.none.fl_str_mv 10.1158/0008-5472.CAN-22-1215
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.14703/260
dc.identifier.journal.none.fl_str_mv Cancer Research
identifier_str_mv 10.1158/0008-5472.CAN-22-1215
Cancer Research
url https://hdl.handle.net/20.500.14703/260
dc.language.iso.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by/4.0/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0/
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv American Association for Cancer Research Inc.
dc.publisher.country.none.fl_str_mv US
publisher.none.fl_str_mv American Association for Cancer Research Inc.
dc.source.none.fl_str_mv reponame:INEN-Institucional
instname:Instituto Nacional de Enfermedades Neoplásicas
instacron:INEN
instname_str Instituto Nacional de Enfermedades Neoplásicas
instacron_str INEN
institution INEN
reponame_str INEN-Institucional
collection INEN-Institucional
repository.name.fl_str_mv Repositorio del Instituto Nacional de Enfermedades Neoplásicas
repository.mail.fl_str_mv repositorio@inen.sld.pe
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