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B cells

IP3R-Mediated Ca2+ Signaling Controls B Cell Proliferation through Metabolic Reprogramming

[iScience] Investigators demonstrated that IP3R-mediated Ca2+ signaling and calcineurin regulated B cell proliferation and survival by activating metabolic reprogramming in response to B cell receptor stimulation.

Elevated BTG2 Improves the Radiosensitivity of Non-small Cell Lung Cancer (NSCLC) through Apoptosis

[Thoracic Cancer] Scientists identified radio-responsive genes and explored the biological function of encoded proteins in NSCLC.

Tumor-Infiltrating B Cells: Immunological Mechanisms, Clinical Impact and Therapeutic Opportunities

[Nature Reviews Cancer] Drawing insights from autoimmunity, scientists review the molecular phenotypes, architectural contexts, antigen specificities, effector mechanisms and regulatory pathways relevant to tumor-infiltrating B lymphocytes in human cancer.

BCL6 and the Notch Pathway: A Signaling Axis Leading to a Novel Druggable Biotarget in Triple Negative Breast Cancer

[Cellular Oncology] Scientists investigated signaling cascades of B cell lymphoma 6 (BCL6) in the CSC compartment of triple negative breast cancers, and the mechanisms that govern its activity, mainly through Notch signaling.

Immune Responses against SARS-CoV-2 Variants after Two and Three Doses of Vaccine in B-cell Malignancies: UK PROSECO Study

[Nature Cancer] The authors presented the PROSECO prospective observational study on 457 patients with lymphoma that received two or three COVID-19 vaccine doses and showed undetectable humoral responses following two vaccine doses in 52% of patients undergoing active anticancer treatment.

Identification of NOXA as a Pivotal Regulator of Resistance to CAR T Cell Therapy in B Cell Malignancies

[Signal Transduction and Targeted Therapy] Via an unbiased genome-wide CRISPR/Cas9 screening, scientists identified loss of NOXA, a B-cell lymphoma 2 family protein in B cell malignancies, as a pivotal regulator of resistance to CAR T cell therapy by impairing apoptosis of tumor cells both in vitro and in vivo.

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