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Oncogenic Vav1-Myo1f induces therapeutically targetable macrophage-rich tumor microenvironment in peripheral T cell lymphoma
Rodriguez Cortes, Jose (Columbia University)
Filip, I. (Columbia University)
Albero Gallego, Robert (Columbia University)
Patiño-Galindo, Juan Ángel (Columbia University)
Aidan Quinn, Stuart (Columbia University)
Lin, W.H.W. (Columbia University)
Laurent, Anouchka (Columbia University)
Shih, Bobby (Columbia University)
Brown, Jessie A. (Columbia University)
Cooke, A.J. (Columbia University)
Mackey, Adam (Columbia University)
Einson, Jonah (Columbia University)
Zairis, Sakellarios (Columbia University)
Rivas-Delgado, Alfredo (Hospital Clínic i Provincial de Barcelona)
Laginestra, Maria Antonella (IRCCS Istituto Ortopedico Rizzoli)
Pileri, Stefano (European Institute of Oncology IRCCS)
Campo, Elias (Hospital Clínic i Provincial de Barcelona)
Bhagat, Govind (Columbia University)
Ferrando, Adolfo A. (Columbia University)
Rabadan, Raul (Columbia University)
Palomero, Teresa (Columbia University)

Data: 2022
Resum: Peripheral T cell lymphoma not otherwise specified (PTCL-NOS) comprises heterogeneous lymphoid malignancies characterized by pleomorphic lymphocytes and variable inflammatory cell-rich tumor microenvironment. Genetic drivers in PTCL-NOS include genomic alterations affecting the VAV1 oncogene; however, their specific role and mechanisms in PTCL-NOS remain incompletely understood. Here we show that expression of Vav1-Myo1f, a recurrent PTCL-associated VAV1 fusion, induces oncogenic transformation of CD4 T cells. Notably, mouse Vav1-Myo1f lymphomas show T helper type 2 features analogous to high-risk GATA3 human PTCL. Single-cell transcriptome analysis reveals that Vav1-Myo1f alters T cell differentiation and leads to accumulation of tumor-associated macrophages (TAMs) in the tumor microenvironment, a feature linked with aggressiveness in human PTCL. Importantly, therapeutic targeting of TAMs induces strong anti-lymphoma effects, highlighting the lymphoma cells' dependency on the microenvironment. These results demonstrate an oncogenic role for Vav1-Myo1f in the pathogenesis of PTCL, involving deregulation in T cell polarization, and identify the lymphoma-associated macrophage-tumor microenvironment as a therapeutic target in PTCL.
Nota: Altres ajuts: National Institutes of Health grants U01CA243073-01, R01CA197945-01, P50CA192937, R01CA256341-01, R35 CA210065, and P30 CA013696
Drets: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, i la comunicació pública de l'obra, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. No es permet la creació d'obres derivades. Creative Commons
Llengua: Anglès
Document: Article ; recerca ; Versió publicada
Publicat a: Cell reports, Vol. 39 Núm. 3 (April 2022) , p. 110695, ISSN 2211-1247

DOI: 10.1016/j.celrep.2022.110695
PMID: 35443168


26 p, 5.9 MB

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