Genetic and epigenetic alterations in pancreatic neuroendocrine tumors.

Pancreatic neuroendocrine tumors (PNETs) epigenetics genetics

Journal

Journal of gastrointestinal oncology
ISSN: 2078-6891
Titre abrégé: J Gastrointest Oncol
Pays: China
ID NLM: 101557751

Informations de publication

Date de publication:
Jun 2020
Historique:
entrez: 14 7 2020
pubmed: 14 7 2020
medline: 14 7 2020
Statut: ppublish

Résumé

Neuroendocrine tumors (NETs) are a heterogenous group of tumors that originate from neuroendocrine cells, mainly in the pancreas and the gastrointestinal and bronchopulmonary tracts. There has been considerable progress in our understanding of the genetic and epigenetic changes associated with pancreatic NETs (PNETs). The main genetic alterations that drive PNETs include genetic alterations in

Identifiants

pubmed: 32655936
doi: 10.21037/jgo.2020.03.11
pii: jgo-11-03-567
pmc: PMC7340809
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

567-577

Informations de copyright

2020 Journal of Gastrointestinal Oncology. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/jgo.2020.03.11). The series “Pancreatic Neuroendocrine Tumors” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.

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Auteurs

Amit Tirosh (A)

Endocrine Oncology Bioinformatics Laboratory, Endocrine Institute Research Center, The Chaim Sheba Medical Center, Tel HaShomer, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Electron Kebebew (E)

Department of Surgery and Stanford Cancer Institute, Stanford University, Stanford, CA, USA.

Classifications MeSH