4.4 Review

Genetics of pancreatic neuroendocrine tumors: implications for the clinic

Journal

EXPERT REVIEW OF GASTROENTEROLOGY & HEPATOLOGY
Volume 9, Issue 11, Pages 1407-1419

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1586/17474124.2015.1092383

Keywords

genetics; islet cell tumor; mutation; pancreatic neuroendocrine tumor; PanNET; sequencing

Funding

  1. National Institute of Health (NIH) [CA62924]
  2. Italian Foundation for the Research on Pancreatic Diseases (FIMP)
  3. Myriad Genetics

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Pancreatic neuroendocrine tumors (PanNETs) are a common and deadly neoplasm of the pancreas. Although the importance of genetic alterations in PanNETs has been known for many years, recent comprehensive sequencing studies have greatly expanded our knowledge of neuroendocrine tumorigenesis in the pancreas. These studies have identified specific cellular processes that are altered in PanNETs, highlighted alterations with prognostic implications, and pointed to pathways for targeted therapies. In this review, we will discuss the genetic alterations that play a key role in PanNET tumorigenesis, with a specific focus on those alterations with the potential to change the way patients with these neoplasms are diagnosed and treated.

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