| Literature DB >> 29458963 |
Davide G Franchina1, Melanie Grusdat1, Dirk Brenner2.
Abstract
Cells of the immune system display varying metabolic profiles to fulfill their functions. B lymphocytes overcome fluctuating energy challenges as they transition from the resting state and recirculation to activation, rapid proliferation, and massive antibody production. Only through a controlled interplay between metabolism, extracellular stimuli, and intracellular signaling can successful humoral responses be mounted. Alterations to this balance can promote malignant transformation of B cells. The metabolic control of B-cell fate is only partially understood. Here, we provide a compelling overview of the current state of the art and describe the main metabolic features of B cells during normal development and oncogenesis, with emphasis on the major B-cell transcriptional and metabolic regulators, including myelocytomatosis virus oncogene cellular homolog (Myc) and hypoxia-inducible factor 1-α (HIF-1α).Entities:
Keywords: B cell; HIF-1α; Myc; immunometabolism; lymphoma
Mesh:
Year: 2018 PMID: 29458963 DOI: 10.1016/j.trecan.2017.12.006
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025