KDM3A/Ets1 epigenetic axis contributes to PAX3/FOXO1-driven and independent disease-promoting gene expression in fusion-positive Rhabdomyosarcoma

Mol Oncol. 2020 Oct;14(10):2471-2486. doi: 10.1002/1878-0261.12769. Epub 2020 Aug 5.

Abstract

Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and young adults. RMS exists as two major disease subtypes, oncofusion-negative RMS (FN-RMS) and oncofusion-positive RMS (FP-RMS). FP-RMS is characterized by recurrent PAX3/7-FOXO1 driver oncofusions and is a biologically and clinically aggressive disease. Recent studies have revealed FP-RMS to have a strong epigenetic basis. Epigenetic mechanisms represent potential new therapeutic vulnerabilities in FP-RMS, but their complex details remain to be defined. We previously identified a new disease-promoting epigenetic axis in RMS, involving the chromatin factor KDM3A and the Ets1 transcription factor. In the present study, we define the KDM3A and Ets1 FP-RMS transcriptomes and show that these interface with the recently characterized PAX3/FOXO1-driven gene expression program. KDM3A and Ets1 positively control numerous known and candidate novel PAX3/FOXO1-induced RMS-promoting genes, including subsets under control of PAX3/FOXO1-associated superenhancers (SE), such as MEST. Interestingly, KDM3A and Ets1 also positively control a number of known and candidate novel FP-RMS-promoting, but not PAX3/FOXO1-dependent, genes. Epistatically, Ets1 is downstream of, and exerts disease-promoting effects similar to, both KDM3A and PAX3/FOXO1. MEST also manifests disease-promoting properties in FP-RMS, and KDM3A and Ets1 each impacts activation of the PAX3/FOXO1-associated MEST SE. Taken together, our studies show that the KDM3A/Ets1 epigenetic axis plays an important role in disease promotion in FP-RMS, and provide insight into potential new ways to target aggressive phenotypes in this disease.

Keywords: Ets1; Jumonji; KDM3A; epigenetics; metastasis; rhabdomyosarcoma.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Line, Tumor
  • Enhancer Elements, Genetic / genetics
  • Epigenesis, Genetic*
  • Forkhead Box Protein O1 / metabolism*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Jumonji Domain-Containing Histone Demethylases / metabolism*
  • Oncogene Proteins, Fusion / metabolism*
  • PAX3 Transcription Factor / metabolism*
  • Phenotype
  • Promoter Regions, Genetic / genetics
  • Proto-Oncogene Protein c-ets-1 / metabolism*
  • Rhabdomyosarcoma / genetics*
  • Transcriptome / genetics

Substances

  • ETS1 protein, human
  • FOXO1 protein, human
  • Forkhead Box Protein O1
  • Oncogene Proteins, Fusion
  • PAX3 Transcription Factor
  • PAX3 protein, human
  • Proto-Oncogene Protein c-ets-1
  • Jumonji Domain-Containing Histone Demethylases
  • KDM3A protein, human