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Record W4405040538 · doi:10.1182/blood-2024-205644

The Arginine Methyltransferase PRMT5 Regulates Maintenance and TKI Resistance of Self-Renewing FLT3-ITD AML LSC

2024· article· en· W4405040538 on OpenAlexaboutno aff
Harish Kumar, Mostafa Mohamed, Aditi Dhir, George M. Burslem, Xinyang Zhao, Rui Lu, Erin Ahn, Ravi Bhatia

Bibliographic record

VenueBlood · 2024
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCancer-related gene regulation
Canadian institutionsnot available
Fundersnot available
KeywordsMyeloid leukemiaProtein arginine methyltransferase 5Cancer researchMethyltransferaseLeukemiaFms-Like Tyrosine Kinase 3MedicineDecitabinePharmacologyBiologyImmunologyMethylationDNA methylation

Abstract

fetched live from OpenAlex

FLT3-ITD mutations are commonly observed in acute myeloid leukemia (AML) and associated with adverse prognosis. FLT3 tyrosine kinase inhibitors (TKIs) demonstrate clinical efficacy but fail to eliminate leukemia stem cells (LSC) leading to treatment failure and relapse. There is a pressing need to understand mechanisms of FLT3-ITD AML LSC persistence and develop strategies to enhance their elimination. Here we show that the type II protein arginine methyltransferase PRMT5 is a critical regulator of FLT3-ITD AML cell maintenance and TKI resistance. To assess the role of epigenetic regulators in FTL3-ITD AML cell maintenance we screened FLT3-ITD AML cell lines using a well-curated collection of epigenetic probes (SGC Toronto). We identified inhibitors of the type II protein arginine methyltransferase PRMT5 to be amongst the top hits. We confirmed dose and time-dependent inhibition of FLT3-ITD AML cells by the PRMT5 inhibitors (PRMT5i), GSK-591 and LLY-283, and showed that combination of PRMT5i with FLT3 TKI (Quizartinib, Giltertinib) synergistically inhibited FLT3-ITD AML cells. Similar results were seen with CRISPR-Cas targeting of PRMT5 in FLT3-ITD AML cells. We further show that PRMT5i reduced the growth of patient-derived primary human FLT3-ITD AML HSPC and enhanced AML HSPC targeting in combination with TKI in vitro, and that the combination of PRMT5i and TKI also significantly enhanced inhibition of AML HSPC growth in PDX models in vivo. PRMT5i also showed activity against primary CD34+ cells from patients FLT3-ITD AML who had relapsed following TKI treatment. Finally, we show that PRMT5i significantly reduced LSC numbers and secondary transplant capacity in a genetic mouse model with FLT3-ITD+ and Tet2 knockout, and enhanced survival of mice after the completion of treatment, with enhanced effect seen in combination with TKI. PRMT5i did not significantly inhibit the growth of normal CD34+ cells in vitro or of normal murine hematopoiesis in vivo. PRMT5 catalyzes the formation of symmetric dimethyl arginine and regulates several histone and nonhistone proteins functioning in RNA processing, transcription, signal transduction and cell cycle regulation. There is growing evidence for an important role for PRMT5 in leukemic and normal hematopoiesis. Ectopic FLT3-ITD expression led to enhanced PRMT5 expression in FLT3-WT cells, whereas FLT3 knockout led to reduced PRMT5 expression in FLT3-ITD cells, supporting a role for FLT3-ITD in modulating PRMT5 expression. FLT3-ITD-mediated PRMT5 regulation appears to be kinase-independent since TKI treatment did not affect PRMT5 expression. RNASeq analysis showed increased p53, inflammatory and apoptosis gene signatures and reduced cell cycling signatures in AML LSK cells following combination treatment. PRMT5i treatment led to enhanced suppression of residual P-Akt, P-MAPK and P-STAT5 levels in TKI-treated AML cells. PRMT5 inhibition and knockdown led to reduced FLT3-ITD protein expression, related to enhanced proteasomal degradation. Finally, we observed that PRMT5i induced an increase in alternative splicing events in FLT3-ITD AML LSK cells, and that TKI treatment while not altering RNA splicing by itself led to a synergistic increase in alternative splicing in combination with PRMT5i treatment. Combination treatment leads to reduced levels of the SR protein kinase and phospho-SR protein levels in FTL3-ITD cells, and depleted phospho-SR proteins from nuclear speckles. We observed increased alternative splicing of genes involved in p53 regulation, Ras/MAPK signaling, growth factor signaling, RNA processing, chromatin modification and transcriptional regulation with combination treatment. We confirmed that combination treatment led to increase in an alternatively spliced MDM4 isoform which was associated with increased p53 and p53 target gene expression. We conclude that PRMT5 plays a critical role in maintenance of self-renewing FLT3-ITD AML LSC and in their persistence following TKI treatment, and that combined PRMT5i and TKI treatment effectively depletes FLT3-ITD AML LSC with disease regenerating capacity. We identify mechanisms underlying the synergistic effects of the combination of PRMT5i with TKI, including depletion of FLT3-ITD protein, activation of the p53 pathway, enhanced inhibition of STAT5, MAPK and AKT signaling, and increased alternative splicing events affecting key LSC maintenance pathways.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.056
Threshold uncertainty score0.426

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.004
GPT teacher head0.214
Teacher spread0.210 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2024
Admission routes1
Has abstractyes

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