Follicular lymphoma dynamics.
Cell of origin (COO)
Committed precursor cell (CPC)
Follicular lymphoma (FL)
Plasticity
Single-cell RNA-seq
Tumor microenvironment
Unmet medical need
Journal
Advances in immunology
ISSN: 1557-8445
Titre abrégé: Adv Immunol
Pays: United States
ID NLM: 0370425
Informations de publication
Date de publication:
2021
2021
Historique:
entrez:
28
6
2021
pubmed:
29
6
2021
medline:
26
10
2021
Statut:
ppublish
Résumé
Follicular lymphoma (FL) is an indolent yet challenging disease. Despite a generally favorable response to immunochemotherapy regimens, a fraction of patients does not respond or relapses early with unfavorable prognosis. For the vast majority of those who initially respond, relapses will repeatedly occur with increasing refractoriness to available treatments. Addressing the clinical challenges in FL warrants deep understanding of the nature of treatment-resistant FL cells seeding relapses, and of the biological basis of early disease progression. Great progress has been made in the last decade in the description and interrogation of the (epi)genomic landscape of FL cells, of their major dependency to the tumor microenvironment (TME), and of the stepwise lymphomagenesis process, from healthy to subclinical disease and to overt FL. A new picture is emerging, in which an ever-evolving tumor-TME duo sparks a complex and multilayered clonal and functional heterogeneity, blurring the discovery of prognostic biomarkers, patient stratification and reliable designs of risk-adapted treatments. Novel technological approaches allowing to decipher both tumor and TME heterogeneity at the single-cell level are beginning to unravel unsuspected cell dynamics and plasticity of FL cells. The upcoming drawing of a comprehensive functional picture of FL within its ecosystem holds great promise to address the unmet medical needs of this complex lymphoma.
Identifiants
pubmed: 34176559
pii: S0065-2776(21)00016-X
doi: 10.1016/bs.ai.2021.05.002
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
43-103Subventions
Organisme : NCI NIH HHS
ID : R01 CA172492
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA260176
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.