Experimental Hematology & Oncology (Jul 2022)

JOSD2 regulates PKM2 nuclear translocation and reduces acute myeloid leukemia progression

  • Hu Lei,
  • Li Yang,
  • Yingying Wang,
  • Zhihui Zou,
  • Meng Liu,
  • Hanzhang Xu,
  • Yingli Wu

DOI
https://doi.org/10.1186/s40164-022-00295-w
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 4

Abstract

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Abstract Pyruvate kinase M2 (PKM2) plays an important role in the metabolism and proliferation of leukemia cells. Here, we show that deubiquitinase JOSD2, a novel tumor suppressor, blocks PKM2 nuclear localization by reducing its K433 acetylation in acute myeloid leukemia (AML). Firstly, we show that JOSD2 is significantly down-regulated in primary AML cells. Reconstitute of JOSD2 in AML cells significantly inhibit cell viability and induce cell apoptosis. Next, PKM2 is identified as a novel interaction protein of JOSD2 by mass spectrometry, co- immunoprecipitation and co-immunofluorescence in HL60 cells. However, JOSD2 does not affect PKM2 protein stability. We then found out that JOSD2 inhibits nuclear localization of PKM2 by reducing its K433 acetylation modification, accompanied by decreased downstream gene expression through non-glycolytic functions. Finally, JOSD2 decreases AML progression in vivo. Taken together, we propose that JOSD2 blocks PKM2 nuclear localization and reduces AML progression.

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