Loss of function mutations of in classical Hodgkin lymphoma.

BCOR is a component of a variant Polycomb repressive complex 1 (PRC1.1). PRC1 and PRC2 complexes together constitute a major gene regulatory system critical for appropriate cellular differentiation. The gene is upregulated in germinal center (GC) B cells and mutated in a number of hematologic malignancies. We report inactivating alterations in 4/7 classic Hodgkin lymphoma (cHL) cell lines, subclonal somatic mutations in Hodgkin and Reed-Sternberg (HRS) cells of 4/10 cHL cases, and deletions in HRS cells of 7/17 primary cHL cases. In mice, conditional loss of driven by AID-Cre in GC B cells resulted in gene expression changes of 46 genes (>2-fold) including upregulated that encodes a transcription factor responsible for establishing T-cell identity and (interleukin-9 receptor), an important member of the cytokine network in cHL. Our findings suggest a role for loss in cHL pathogenesis and GC-B cell homeostasis.