Unraveling the Role of the NLRP3 Inflammasome in Lymphoma: Implications in Pathogenesis and Therapeutic Strategies

Int J Mol Sci. 2024 Feb 17;25(4):2369. doi: 10.3390/ijms25042369.

Abstract

Inflammasomes are multimeric protein complexes, sensors of intracellular danger signals, and crucial components of the innate immune system, with the NLRP3 inflammasome being the best characterized among them. The increasing scientific interest in the mechanisms interconnecting inflammation and tumorigenesis has led to the study of the NLRP3 inflammasome in the setting of various neoplasms. Despite a plethora of data regarding solid tumors, NLRP3 inflammasome's implication in the pathogenesis of hematological malignancies only recently gained attention. In this review, we investigate its role in normal lymphopoiesis and lymphomagenesis. Considering that lymphomas comprise a heterogeneous group of hematologic neoplasms, both tumor-promoting and tumor-suppressing properties were attributed to the NLRP3 inflammasome, affecting neoplastic cells and immune cells in the tumor microenvironment. NLRP3 inflammasome-related proteins were associated with disease characteristics, response to treatment, and prognosis. Few studies assess the efficacy of NLRP3 inflammasome therapeutic targeting with encouraging results, though most are still at the preclinical level. Further understanding of the mechanisms regulating NLRP3 inflammasome activation during lymphoma development and progression can contribute to the investigation of novel treatment approaches to cover unmet needs in lymphoma therapeutics.

Keywords: NLRP3; inflammasome; inflammatory signaling; lymphoma; lymphomagenesis; lymphopoiesis; pyroptosis.

Publication types

  • Review

MeSH terms

  • Humans
  • Inflammasomes* / metabolism
  • Inflammation / metabolism
  • Lymphoma* / etiology
  • Lymphoma* / therapy
  • NLR Family, Pyrin Domain-Containing 3 Protein / metabolism
  • Tumor Microenvironment

Substances

  • Inflammasomes
  • NLR Family, Pyrin Domain-Containing 3 Protein

Grants and funding

This research received no external funding.