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Updated: Jan 14, 2026

Intracellular Phosphoflow Cytometry of Acute Myeloid Leukemia Patient-Derived Xenotransplants
Published on: June 6, 2025
The proteostasis network is a therapeutic target in acute myeloid leukemia
Kentson Lam1, Yoon Joon Kim1, Evelyn Li-Ting Tan1
1Division of Regenerative Medicine, Department of Medicine, Stem Cell Discovery Center, Sanford Stem Cell Institute, Moores Cancer Center, University of California San Diego, La Jolla, CA.
Abstract:
Oncogenic growth places great strain and dependence on protein homeostasis (proteostasis). This has made proteostasis pathways attractive therapeutic targets in cancer, but efforts to drug these pathways have yielded disappointing clinical outcomes. One exception is proteasome inhibitors, which are approved for the frontline treatment of multiple myeloma. However, proteasome inhibitors are largely ineffective for the treatment of other cancers at tolerable doses, including acute myeloid leukemia (AML), although reasons for these differences are unknown. Here, we determined that proteasome inhibitors are ineffective in AML due to their inability to disrupt proteostasis. In response to proteasome inhibition, AML cells activated HSF1 and increased autophagic flux to preserve proteostasis. Genetic inactivation of HSF1 sensitized AML cells to proteasome inhibition, marked by accumulation of unfolded protein, activation of the protein kinase R (PKR)-like endoplasmic reticulum kinase (PERK)-mediated integrated stress response, severe reductions in protein synthesis, proliferation and cell survival, and significant slowing of disease progression and extension of survival in vivo. Similarly, combined autophagy and proteasome inhibition suppressed proliferation, synergistically killed human AML cells, and significantly reduced AML burden and extended survival in vivo. Furthermore, autophagy and proteasome inhibition preferentially suppressed protein synthesis and colony formation and induced apoptosis in cells from patients with primary AML, including AML stem/progenitor cells, compared with normal hematopoietic stem/progenitor cells. Combined autophagy and proteasome inhibition activated a terminal integrated stress response, which was surprisingly PKR. These studies unravel how proteostasis pathways are coopted to promote AML growth, progression and drug resistance and reveal that disabling the proteostasis network is a promising strategy to therapeutically target AML.
Insights
Acute myeloid leukemia (AML) cells resist proteasome inhibitors by maintaining protein homeostasis (proteostasis) via HSF1 and autophagy. Targeting these pathways, alongside proteasome inhibitors, offers a promising therapeutic strategy for AML.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Cancer cells rely on protein homeostasis (proteostasis) for survival, making proteostasis pathways attractive therapeutic targets.
- Proteasome inhibitors are effective in multiple myeloma but largely ineffective in acute myeloid leukemia (AML) due to unknown reasons.
- Understanding AML's resistance mechanisms to proteasome inhibitors is crucial for developing effective treatments.
Purpose of the Study:
- To investigate why proteasome inhibitors are ineffective in AML.
- To explore therapeutic strategies targeting proteostasis pathways in AML.
- To identify key mechanisms of drug resistance in AML.
Main Methods:
- Investigated proteostasis mechanisms in AML cells upon proteasome inhibition.
- Utilized genetic inactivation of HSF1 and combined autophagy and proteasome inhibition.
- Assessed effects on protein synthesis, proliferation, apoptosis, and in vivo disease progression.
- Analyzed responses in primary patient AML cells versus normal hematopoietic stem/progenitor cells.
Main Results:
- AML cells activate HSF1 and increase autophagic flux to maintain proteostasis against proteasome inhibitors.
- Genetic inactivation of HSF1 sensitizes AML cells to proteasome inhibition, reducing proliferation and extending survival.
- Combined autophagy and proteasome inhibition synergistically kill AML cells, preferentially targeting AML stem/progenitor cells.
- This combination therapy induces a terminal integrated stress response driven by Protein kinase R (PKR).
Conclusions:
- AML cells co-opt proteostasis pathways (HSF1, autophagy) for growth, progression, and drug resistance.
- Disrupting the proteostasis network by combining autophagy and proteasome inhibition is a promising therapeutic strategy for AML.
- This approach shows preferential efficacy against AML cells, including stem/progenitor populations, compared to normal cells.
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