Notch Signaling Promotes Mature T-Cell Lymphomagenesis
Descripción del Articulo
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...
| Autores: | , , , , , , , , , , , , , , , , , , , |
|---|---|
| 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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INEN_22752eba01cb909637b8fb1dff1c7cc4 |
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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 |
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INEN-Institucional |
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INEN-Institucional |
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Repositorio del Instituto Nacional de Enfermedades Neoplásicas |
| repository.mail.fl_str_mv |
repositorio@inen.sld.pe |
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1868438565489213440 |
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12.824051 |
Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).