Genomic patterns of malignant peripheral nerve sheath tumour (MPNST) evolution correlate with clinical outcome and are detectable in cell-free DNA

Cortes-Ciriano, I.; Steele, C. D.; Piculell, K. G.; Al-Ibraheemi, A.; Eulo, V.; Bui, M. M.; Chatzipli, A.; Dickson, B. C.; Borcherding, D. C.; Feber, A.; Galor, A.; Hart, J.; Jones, K. B.; Jordan, J. T.; Kim, R. H.; Lindsay, D.; Miller, C.; Nishida, Y.; Proszek, P.; Serrano, J.; Sundby, R. T.; Szymanski, J. J.; Ullrich, N. J.; Viskochil, D.; Wang, X.; Snuderl, M.; Park, P. J.; Flanagan, A. M.; Hirbe, A. C.; Pillay, N.; Miller, D. T.

doi:10.1101/2022.05.03.490481

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bioRxiv · 10.1101/2022.05.03.490481

Genomic patterns of malignant peripheral nerve sheath tumour (MPNST) evolution correlate with clinical outcome and are detectable in cell-free DNA

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Abstract

Malignant peripheral nerve sheath tumour (MPNST) is an aggressive soft-tissue sarcoma that arises in peripheral nerves. MPNST occurs either sporadically or in people with neurofibromatosis type 1 (NF1), a common cancer predisposition syndrome caused by germline pathogenic variants in NF1. Although MPNST is the most common cause of death and morbidity for individuals with NF1, the molecular underpinnings of MPNST pathogenesis remain unclear. Here, we report the analysis of whole-genome sequencing, multi-regional exome sequencing, transcriptomic and methylation profiling data for 95 MPNSTs and precursor lesions (64 NF1-related; 31 sporadic) from 77 individuals. Early events in tumour evolution include biallelic inactivation of NF1 followed by inactivation of CDKN2A and in some cases also TP53 and polycomb repressive complex 2 (PRC2) genes. Subsequently, both sporadic and NF1-related MPNSTs acquire a high burden of somatic copy number alterations (SCNAs). Our analysis revealed distinct pathways of tumour evolution and immune infiltration associated with inactivation of PRC2 genes and H3K27 trimethylation (H3K27me3) status. Tumours with loss of H3K27me3 evolve through extensive chromosomal losses with retention of chromosome 8 heterozygosity followed by whole genome doubling and chromosome 8 amplification. These tumours show lower levels of immune cell infiltration with low cytotoxic activity and low expression of immune checkpoints. In contrast, tumours with retention of H3K27me3 evolve through extensive genomic instability in the absence of recurrent alterations and exhibit an immune cell-rich phenotype. Specific SCNAs detected in both tumour samples and cell-free DNA (cfDNA) act as a surrogate for loss of H3K27me3 and immune infiltration, and predict prognosis. Our results suggest that SCNA profiling of tumour or cfDNA could serve as a biomarker for early diagnosis and to stratify patients into prognostic and treatment-related subgroups.

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Cortes-Ciriano, I., Steele, C. D., Piculell, K. G., Al-Ibraheemi, A., Eulo, V., Bui, M. M., Chatzipli, A., Dickson, B. C., Borcherding, D. C., Feber, A., Galor, A., Hart, J., Jones, K. B., Jordan, J. T., Kim, R. H., Lindsay, D., Miller, C., Nishida, Y., Proszek, P., Serrano, J., Sundby, R. T., Szymanski, J. J., Ullrich, N. J., Viskochil, D., Wang, X., Snuderl, M., Park, P. J., Flanagan, A. M., Hirbe, A. C., Pillay, N., Miller, D. T.. 2022-05-05. Genomic patterns of malignant peripheral nerve sheath tumour (MPNST) evolution correlate with clinical outcome and are detectable in cell-free DNA. https://doi.org/10.1101/2022.05.03.490481

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