Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands.

Abstract:

:The molecular pathogenesis of salivary gland acinic cell carcinoma (AciCC) is poorly understood. The secretory Ca-binding phosphoprotein (SCPP) gene cluster at 4q13 encodes structurally related phosphoproteins of which some are specifically expressed at high levels in the salivary glands and constitute major components of saliva. Here we report on recurrent rearrangements [t(4;9)(q13;q31)] in AciCC that translocate active enhancer regions from the SCPP gene cluster to the region upstream of Nuclear Receptor Subfamily 4 Group A Member 3 (NR4A3) at 9q31. We show that NR4A3 is specifically upregulated in AciCCs, and that active chromatin regions and gene expression signatures in AciCCs are highly correlated with the NR4A3 transcription factor binding motif. Overexpression of NR4A3 in mouse salivary gland cells increases expression of known NR4A3 target genes and has a stimulatory functional effect on cell proliferation. We conclude that NR4A3 is upregulated through enhancer hijacking and has important oncogenic functions in AciCC.

journal_name

Nat Commun

journal_title

Nature communications

authors

Haller F,Bieg M,Will R,Körner C,Weichenhan D,Bott A,Ishaque N,Lutsik P,Moskalev EA,Mueller SK,Bähr M,Woerner A,Kaiser B,Scherl C,Haderlein M,Kleinheinz K,Fietkau R,Iro H,Eils R,Hartmann A,Plass C,Wiemann S,Aga

doi

10.1038/s41467-018-08069-x

subject

Has Abstract

pub_date

2019-01-21 00:00:00

pages

368

issue

1

issn

2041-1723

pii

10.1038/s41467-018-08069-x

journal_volume

10

pub_type

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