BDNF/TrkB confers bortezomib resistance in multiple myeloma by inducing BRINP3

Biochim Biophys Acta Gen Subj. 2023 Mar;1867(3):130299. doi: 10.1016/j.bbagen.2022.130299. Epub 2022 Dec 21.

Abstract

Background: The proteasome inhibitor bortezomib (BTZ) has significantly improved the survival of multiple myeloma (MM) patients. However, most MM patients still relapse and have drug resistance after BTZ treatment.

Methods: siRNA transfection was performed to knock down BDNF and TrkB expression. ELISA, western blot, quantitative polymerase chain reaction, CCK-8 assay, and flow cytometry analysis were performed to analyze the functions of BDNF/TrkB signaling in MM cells.

Results: We identified a cell-autonomous mechanism that promotes BTZ resistance in MM, prolongs their RPMI 8226/BTZ resistant cell survival and optimizes their proliferating function. Specifically, RPMI 8226/BTZ cells produced the brain derived neurotrophic factor (BDNF) and its receptor TrkB, which served as a survival factor in the RPMI 8226/BTZ resistant environment. BDNF/TrkB induced phosphorylation of STAT3 that upregulated the bone morphogenetic protein/retinoic acid inducible neural-specific 3 (BRINP3).

Conclusions: BDNF/TrkB enhanced downstream pathway expression of phosphorylation STAT3 and BRINP3 molecules, promoting RPMI 8226/BTZ cell proliferation and survival.

General significance: These data place BDNF/TrkB at the top of a pSTAT3-BRINP3 survival pathway and link adaptability to BTZ resistant conditions in MM disease.

Keywords: BDNF; BRINP3; Bortezomib resistance; Multiple myeloma; TrkB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bortezomib / pharmacology
  • Brain-Derived Neurotrophic Factor
  • Cell Line, Tumor
  • Humans
  • Multiple Myeloma* / drug therapy
  • Multiple Myeloma* / metabolism
  • Proteasome Inhibitors / pharmacology

Substances

  • Bortezomib
  • Brain-Derived Neurotrophic Factor
  • Proteasome Inhibitors