Estrogen receptor ? wields treatment-specific enhancers between morphologically similar endometrial tumors.

ABSTRACT: The DNA-binding sites of estrogen receptor ? (ER?) show great plasticity under the control of hormones and endocrine therapy. Tamoxifen is a widely applied therapy in breast cancer that affects ER? interactions with coregulators and shifts the DNA-binding signature of ER? upon prolonged exposure in breast cancer. Although tamoxifen inhibits the progression of breast cancer, it increases the risk of endometrial cancer in postmenopausal women. We therefore asked whether the DNA-binding signature of ER? differs between endometrial tumors that arise in the presence or absence of tamoxifen, indicating divergent enhancer activity for tumors that develop in different endocrine milieus. Using ChIP sequencing (ChIP-seq), we compared the ER? profiles of 10 endometrial tumors from tamoxifen users with those of six endometrial tumors from nonusers and integrated these results with the transcriptomic data of 47 endometrial tumors from tamoxifen users and 64 endometrial tumors from nonusers. The ER?-binding sites in tamoxifen-associated endometrial tumors differed from those in the tumors from nonusers and had distinct underlying DNA sequences and divergent enhancer activity as marked by histone 3 containing the acetylated lysine 27 (H3K27ac). Because tamoxifen acts as an agonist in the postmenopausal endometrium, similar to estrogen in the breast, we compared ER? sites in tamoxifen-associated endometrial cancers with publicly available ER? ChIP-seq data in breast tumors and found a striking resemblance in the ER? patterns of the two tissue types. Our study highlights the divergence between endometrial tumors that arise in different hormonal conditions and shows that ER? enhancer use in human cancer differs in the presence of nonphysiological endocrine stimuli.

SUBMITTER: Droog M 

PROVIDER: S-EPMC5338442 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature