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• W3213571080 abstract "Rhabdomyosarcomas (RMS) represent a family of aggressive soft tissue sarcomas that present in both children and adults. Pathologic risk stratification for RMS has been based on histologic subtype, with poor outcomes observed in alveolar rhabdomyosarcoma (ARMS) and the adult-type pleomorphic rhabdomyosarcoma (PRMS) compared to embryonal rhabdomyosarcoma (ERMS). Genomic sequencing studies have expanded the spectrum of RMS, with several new molecularly defined entities, including fusion-driven spindle cell/sclerosing rhabdomyosarcoma (SC/SRMS) and MYOD1-mutant SC/SRMS. Comprehensive genomic analysis has previously defined the mutational and copy number spectrum for the more common ERMS and ARMS and revealed corresponding methylation signatures. Comparatively, less is known about epigenetic correlates for the rare SC/SRMS or PRMS histologic subtypes. Herein, we present exome and RNA sequencing, copy number analysis, and methylation profiling of the largest cohort of molecularly characterized RMS samples to date. In addition to ARMS and ERMS, we identify two novel methylation subtypes, one having SC/SRMS histology and defined by MYOD1 p. L122R mutations and the other matching adult-type PRMS. Selected tumors from adolescent patients grouped with the PRMS methylation class, expanding the age range of these rare tumors. Limited follow-up data suggest that pediatric tumors with MYOD1-mutations are associated with an aggressive clinical course." @default.
• W3213571080 created "2021-11-22" @default.
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• W3213571080 date "2021-11-15" @default.
• W3213571080 modified "2023-10-16" @default.
• W3213571080 title "Methylation profiling reveals novel molecular classes of rhabdomyosarcoma" @default.
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• W3213571080 doi "https://doi.org/10.1038/s41598-021-01649-w" @default.
• W3213571080 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8592993" @default.
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• W3213571080 hasPublicationYear "2021" @default.
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