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Home » Keywords » Burkitt lymphoma

Items Tagged with 'Burkitt lymphoma'

ARTICLES

3D illustration of B-cell lymphoma
Cancer

Targeting Crlz-1: new peptide therapy shows antilymphoma effects

March 4, 2025

The nuclear protein charged amino acid-rich leucine zipper 1 (Crlz-1) has been shown to play a role in the rapid proliferative stages of B-cell development, being targeted by the canonical Wnt/β-catenin signaling pathway.


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Malignant B-cell lymphocytes seen in Burkitt lymphoma, stained with hematoxylin and eosin (H&E) stain.
Immuno-oncology

Gp350‑targeted CAR T-cell therapy exhibits preclinical efficacy in EBV-positive Burkitt lymphoma

Feb. 27, 2025
Epstein-Barr virus (EBV), a member of the herpesvirus family, is a highly common human pathogen that can remain latent in B lymphocytes after the primary infection. Although this latent state is frequently asymptomatic, in some cases, it can lead to the development of malignancies such as Burkitt lymphoma, Hodgkin lymphoma, nasopharyngeal carcinoma, and some gastric cancer subtypes.
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Cancer

Shanghai Xucheng Pharmatech patents new DNA repair protein RAD51 homolog 1 inhibitors

May 31, 2023
Shanghai Xucheng Pharmatech Co. Ltd. has disclosed DNA repair protein RAD51 homolog 1...
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Cancer

Gluetacs Therapeutics discovers new BTK and GSPT1 degradation inducers

Feb. 10, 2023
Gluetacs Therapeutics (Shanghai) Co. Ltd. has described proteolysis targeting chimera (PROTAC) compounds comprising E3 ubiquitin ligase binding moiety covalently linked to a Bruton tyrosine kinase (BTK) and eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) targeting moiety through a linker reported to be useful for the treatment of cancer, anemia, transplant rejection, neurodegeneration, infections, autoimmune, inflammatory and metabolic disorders.
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Cancer

Nihon Medi-Physics has disclosed new ADCs for cancer

Nov. 17, 2022
Nihon Medi-Physics Co. Ltd. has identified antibody-drug conjugates (ADCs) comprising a peptide-modified antibody targeting B-lymphocyte antigen CD20 covalently linked to a radionuclide-chelating agent through a linker reported to be useful for the diagnosis and treatment of cancer.
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