Genetics of pancreatic neuroendocrine tumors: implications for the clinic

Expert Rev Gastroenterol Hepatol. 2015;9(11):1407-19. doi: 10.1586/17474124.2015.1092383. Epub 2015 Sep 28.

Abstract

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.

Keywords: PanNET; genetics; islet cell tumor; mutation; pancreatic neuroendocrine tumor; sequencing.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers, Tumor / genetics*
  • DNA Mutational Analysis
  • Genetic Predisposition to Disease
  • Humans
  • Mutation*
  • Neuroendocrine Tumors / genetics*
  • Neuroendocrine Tumors / pathology
  • Neuroendocrine Tumors / therapy
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / pathology
  • Pancreatic Neoplasms / therapy
  • Phenotype
  • Precision Medicine
  • Predictive Value of Tests
  • Prognosis
  • Risk Factors

Substances

  • Biomarkers, Tumor