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Sci Rep DOI:10.1038/srep25521

Recurrent hormone-binding domain truncated ESR1 amplifications in primary endometrial cancers suggest their implication in hormone independent growth.

Publication TypeJournal Article
Year of Publication2016
AuthorsHolst, F, Hoivik, EA, Gibson, WJ, Taylor-Weiner, A, Schumacher, SE, Asmann, YW, Grossmann, P, Trovik, J, Necela, BM, E Thompson, A, Meyerson, M, Beroukhim, R, Salvesen, HB, Cherniack, AD
JournalSci Rep
Volume6
Pages25521
Date Published2016 May 10
ISSN2045-2322
Abstract

The estrogen receptor alpha (ERα) is highly expressed in both endometrial and breast cancers, and represents the most prevalent therapeutic target in breast cancer. However, anti-estrogen therapy has not been shown to be effective in endometrial cancer. Recently it has been shown that hormone-binding domain alterations of ERα in breast cancer contribute to acquired resistance to anti-estrogen therapy. In analyses of genomic data from The Cancer Genome Atlas (TCGA), we observe that endometrial carcinomas manifest recurrent ESR1 gene amplifications that truncate the hormone-binding domain encoding region of ESR1 and are associated with reduced mRNA expression of exons encoding the hormone-binding domain. These findings support a role for hormone-binding alterations of ERα in primary endometrial cancer, with potentially important therapeutic implications.

URLhttp://dx.doi.org/10.1038/srep25521
DOI10.1038/srep25521
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/27160768?dopt=Abstract

Alternate JournalSci Rep
PubMed ID27160768
PubMed Central IDPMC4861919
Grant ListF30 CA192725 / CA / NCI NIH HHS / United States
T32 GM007753 / GM / NIGMS NIH HHS / United States