| Literature DB >> 29866822 |
Matthew L Hemming1,2, Matthew A Lawlor3, Rhamy Zeid3, Tom Lesluyes4,5, Jonathan A Fletcher6, Chandrajit P Raut7, Ewa T Sicinska8, Frédéric Chibon9,10, Scott A Armstrong11, George D Demetri2,12, James E Bradner1.
Abstract
Activating mutations in the KIT or PDGFRA receptor tyrosine kinases are hallmarks of gastrointestinal stromal tumor (GIST). The biological underpinnings of recurrence following resection or disease progression beyond kinase mutation are poorly understood. Utilizing chromatin immunoprecipitation with sequencing of tumor samples and cell lines, we describe the enhancer landscape of GIST, highlighting genes that reinforce and extend our understanding of these neoplasms. A group of core transcription factors can be distinguished from others unique to localized and metastatic disease. The transcription factor HAND1 emerges in metastatic disease, binds to established GIST-associated enhancers, and facilitates GIST cell proliferation and KIT gene expression. The pattern of transcription factor expression in primary tumors is predictive of metastasis-free survival in GIST patients. These results provide insight into the enhancer landscape and transcription factor network underlying GIST, and define a unique strategy for predicting clinical behavior of this disease.Entities:
Keywords: GIST; epigenetics; sarcoma; transcription factor
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Year: 2018 PMID: 29866822 PMCID: PMC6016782 DOI: 10.1073/pnas.1802079115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205