TERT structural rearrangements in metastatic pheochromocytomas. Issue 1 (January 2018)

• Record Type: Journal Article
• Authors: Dwight, Trisha; Flynn, Aidan; Amarasinghe, Kaushalya; Benn, Diana E; Lupat, Richard; Li, Jason; Cameron, Daniel L; Hogg, Annette; Balachander, Shiva; Candiloro, Ida L M; Wong, Stephen Q; Robinson, Bruce G; Papenfuss, Anthony T; Gill, Anthony J; Dobrovic, Alexander; Hicks, Rodney J; Clifton-Bligh, Roderick J; Tothill, Richard W
• Is Part Of: Endocrine-related cancer. Volume 25:Issue 1(2018)
• Page Start: 1
• Page End: 9
• Publication Date: 2018-01
• Subjects: TERT -- pheochromocytoma -- metastatic -- whole genome sequencing -- rearrangements; Endocrine glands -- Cancer -- Periodicals; Endocrinology -- Periodicals; Cancer -- Endocrine aspects -- Periodicals; 616.9944005
• DOI: 10.1530/ERC-17-0306
• Languages: English
• ISSNs: 1351-0088

Abstract

Abstract : Pheochromocytomas (PC) and paragangliomas (PGL) are endocrine tumors for which the genetic and clinicopathological features of metastatic progression remain incompletely understood. As a result, the risk of metastasis from a primary tumor cannot be predicted. Early diagnosis of individuals at high risk of developing metastases is clinically important and the identification of new biomarkers that are predictive of metastatic potential is of high value. Activation of TERT has been associated with a number of malignant tumors, including PC/PGL. However, the mechanism of TERT activation in the majority of PC/PGL remains unclear. As TERT promoter mutations occur rarely in PC/PGL, we hypothesized that other mechanisms – such as structural variations – may underlie TERT activation in these tumors. From 35 PC and four PGL, we identified three primary PCs that developed metastases with elevated TERT expression, each of which lacked TERT promoter mutations and promoter DNA methylation. Using whole genome sequencing, we identified somatic structural alterations proximal to the TERT locus in two of these tumors. In both tumors, the genomic rearrangements led to the positioning of super-enhancers proximal to the TERT promoter, that are likely responsible for the activation of the normally tightly repressed TERT expression in chromaffin cells