Results 61 to 70 of about 616,871 (170)

Identification of novel Menin-MLL interaction inhibitors targeting leukemia using in-silico virtual screening and structure-based drug design approaches

open access: yesJournal of Genetic Engineering and Biotechnology
Leukemogenesis fundamentally depends on the interaction between Menin and MLL1 fusion proteins, especially in the context of aggressive mixed-lineage leukemia (MLL)-rearranged subtypes.
Amany I. Almars, Shahad W. Kattan
doaj   +1 more source

MLL oncoprotein levels influence leukemia lineage identities

open access: yesNature Communications
Chromosomal translocations involving the mixed-lineage leukemia (MLL) locus generate potent oncogenic fusion proteins (oncoproteins) that disrupt regulation of developmental gene expression.
Derek H. Janssens   +11 more
doaj   +1 more source

Research Progress on the KMT2A-AFF3 Fusion Gene in Childhood Acute Lymphoblastic Leukemia: Mechanisms, Clinical Implications, and Therapeutic Strategies

open access: yesCurrent Issues in Molecular Biology
KMT2A-rearranged (KMT2A-r) acute lymphoblastic leukemia (ALL), particularly in infants, represents one of the most aggressive pediatric hematological malignancies with a historically dismal prognosis.
Yawei Zhang, Juan Liang
doaj   +1 more source

Epigenetic regulation of noncanonical menin targets modulates menin inhibitor response in acute myeloid leukemia

open access: yesBlood
Abstract Menin inhibitors that disrupt the menin-MLL interaction hold promise for treating specific acute myeloid leukemia (AML) subtypes, including those with KMT2A rearrangements (KMT2A-r), yet resistance remains a challenge. Here, through systematic chromatin-focused CRISPR screens, along with genetic, epigenetic,
Xinyue Zhou   +13 more
openaire   +2 more sources

Glucose-Mediated Repression of Menin Promotes Pancreatic β-Cell Proliferation

open access: yes, 2012
Menin, encoded by the Men1 gene, is responsible for β-cell tumor formation in patients with multiple endocrine neoplasia type 1. Recently, menin has been proven to negatively regulate β-cell proliferation during pregnancy.
Fengying Li   +12 more
core   +1 more source

Mario Menin. camicia nera futurista e primo battaglista del mondo

open access: yes
Mario Menin : camicia nera futurista e primo battaglista del mondo / (presentazione di Filippo Tommaso Marinetti e Luigi Scrivo). - Roma : Edizioni futuriste di poesia, stampa 1941 Dedica manoscritta dell\u27autore: A Bodrero Emilio / con ammirazione ...
Menin, Mario
core  

Menin maintains enhancer-promoter interactions in a leukemia-specific manner [PDF]

open access: yes
Inhibition of the protein-protein interaction between Mixed Lineage Leukemia (MLL/KMT2A) protein and the adapter protein Menin is a promising therapy for both high-risk MLL-rearranged and NPM1-mutant (NPM1c) acute leukemias.
Kessler, Benedikt   +15 more
core   +1 more source

Upfront menin-inhibitor resistance in multiply pretreated leukemias

open access: yesExperimental Hematology
Inhibitors of the menin-KMT2A interaction are promising agents for the treatment of KMT2A-rearranged leukemias. We evaluated menin inhibition in patient-derived xenografts of KMT2A-rearranged leukemias with high-risk features. Three acute myeloid leukemias with high-risk fusion partners (mixed-lineage leukemia-10 [MLLT10] and mixed-lineage leukemia-4 ...
Leila Mahdavi   +18 more
openaire   +2 more sources

Targeted and epigenetic therapies for acute myeloid leukemia treatment

open access: yesDiscover Oncology
This article provides a comprehensive overview of targeted and epigenetic therapies for acute myeloid leukemia (AML), highlighting their role in advancing treatment strategies.
Marzieh Shokoohi   +5 more
doaj   +1 more source

Synergistic targeting of KMT2A-rearranged AML with combined LSD1 and menin inhibitors

open access: yes
KMT2A-rearranged (KMT2Ar) acute myeloid leukemia (AML) is a high-risk subtype of AML associated with poor prognosis and frequent relapse. Standard therapies often fail to achieve durable remission, underscoring the urgent need for novel treatments. Menin
Beckedorff, Felipe   +11 more
core   +1 more source

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