| Literature DB >> 35027991 |
Daniel Dai Yu1, Jianzhong Zhang2.
Abstract
Angioimmunoblastic T-cell lymphoma (AITL) is a subtype of peripheral T cell lymphoma (PTCL), defined by genetic alterations that induce abnormal immune activity and inflammatory disorders. Through recent discoveries using genomic studies, the identification of various recurrent mutations has provided greater insight and changed our understanding of the molecular genetics of the disease. By acknowledging these recurrent mutations and their affected pathways, the diagnosis, prognosis, treatment, and survival of AITL can be improved. In this review, we summarize the known recurrent mutations present in the molecular pathogenesis of AITL by emphasizing the effects of mutations on signaling pathways and genes, as well as the multistep process of AITL development. IJCEPEntities:
Keywords: AITL; DNMT3A; IDH2; RHOA; T-cell receptor signaling; TET2
Year: 2021 PMID: 35027991 PMCID: PMC8748014
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625