PRMT5 inhibition preferentially targets MYCN-amplified neuroblastoma via altered transcriptional and splicing programmes regulating key cancer cell fitness pathways.

Bojko, J.; Kollareddy, M.; Szemes, M.; Bellamy, J.; Poon, E.; Moukachar, A.; Legge, D.; Vincent, E. E.; Jones, N.; Malik, S.; Greenhough, A.; Paterson, A.; Park, J. H.; Gallacher, K.; Chesler, L.; Malik, K.

doi:10.1101/2024.02.28.582087

bioRxiv · 10.1101/2024.02.28.582087

PRMT5 inhibition preferentially targets MYCN-amplified neuroblastoma via altered transcriptional and splicing programmes regulating key cancer cell fitness pathways.

Bojko, J.·Kollareddy, M.·Szemes, M.·Bellamy, J.·Poon, E.·Moukachar, A.·Legge, D.·Vincent, E. E.·Jones, N.·Malik, S.·Greenhough, A.·Paterson, A.·Park, J. H.·Gallacher, K.·Chesler, L.·Malik, K.

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Abstract

About 50% of poor prognosis neuroblastoma arises due to MYCN over-expression. We previously demonstrated that MYCN and PRMT5 proteins interact and PRMT5 knockdown led to apoptosis of MYCN amplified (MNA) neuroblastoma. Here we evaluate PRMT5 inhibitors GSK3203591/GSK3326593 as targeted therapeutics for MNA neuroblastoma and show MYCN-dependent growth inhibition and apoptosis. RNAseq revealed dysregulated MYCN transcriptional programmes and altered mRNA splicing, converging on key regulatory pathways such as DNA damage response, epitranscriptomics and cellular metabolism. Metabolic tracing showed glutamine metabolism was impeded following GSK3203591 treatment, which disrupted the MLX/Mondo nutrient sensors via intron retention of MLX mRNA. Glutaminase (GLS) protein was decreased by GSK3203591 despite unchanged transcript levels, suggesting post-transcriptional regulation. We demonstrate the RNA methyltransferase METTL3 and cognate reader YTHDF3 proteins are lowered following splicing alterations; accordingly, we observed hypomethylation of GLS mRNA and decreased GLS following YTHDF3 knockdown. In vivo efficacy of GSK3326593 was confirmed by increased survival of Th-MYCN mice together with splicing events and protein decreases consistent with in vitro data. Our study supports the spliceosome as a key vulnerability of MNA neuroblastoma and rationalises PRMT5 inhibition as a targeted therapy. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=133 SRC="FIGDIR/small/582087v2_ufig1.gif" ALT="Figure 1"> View larger version (54K): org.highwire.dtl.DTLVardef@1ac6b5org.highwire.dtl.DTLVardef@1eb9520org.highwire.dtl.DTLVardef@18b980corg.highwire.dtl.DTLVardef@1ab46e0_HPS_FORMAT_FIGEXP M_FIG C_FIG

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Bojko, J., Kollareddy, M., Szemes, M., Bellamy, J., Poon, E., Moukachar, A., Legge, D., Vincent, E. E., Jones, N., Malik, S., Greenhough, A., Paterson, A., Park, J. H., Gallacher, K., Chesler, L., Malik, K.. 2024-03-02. PRMT5 inhibition preferentially targets MYCN-amplified neuroblastoma via altered transcriptional and splicing programmes regulating key cancer cell fitness pathways.. https://doi.org/10.1101/2024.02.28.582087

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