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The Role of Genetics in Sporadic GEP-NETs: A Comprehensive Review of the Literature

Open Access
|Jun 2017

Abstract

Neuroendocrine tumors (NETs) are composed of a heterogeneous group of malignancies from neuroendocrine cell compartments, with roles in both the endocrine and the nervous system. The majority of NETs are gastroenteropancreatic (GEP) in origin, arising in the foregut, midgut, or hindgut. The genomic landscape of GEP-NETs has been scarcely studied in terms of genomic profiling.The following algorithm was followed using the keywords neuroendocrine, genomics, targeted therapy, personalized medicine, gastroenteropancreatic and NET. The search was performed in PubMed and ScienceDirect database. Our current knowledge of sporadic GEP-NETs genetics must be further advanced to elucidate the molecular basis and pathogenesis of the disease, improve the accuracy of diagnosis, and guide tailor-made therapies.

DOI: https://doi.org/10.1515/fco-2017-0001 | Journal eISSN: 1792-362X | Journal ISSN: 1792-345X
Language: English
Page range: 1 - 5
Submitted on: Nov 28, 2016
Accepted on: May 14, 2017
Published on: Jun 30, 2017
Published by: Helenic Society of Medical Oncology
In partnership with: Paradigm Publishing Services
Publication frequency: 2 times per year

© 2017 George Fotopoulos, Ioannis Vathiotis, George C. Nikou, Konstantinos Syrigos, published by Helenic Society of Medical Oncology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.