Racial disparity in gastrointestinal cancer risk

H Ashktorab, SS Kupfer, H Brim, JM Carethers - Gastroenterology, 2017 - Elsevier
Cancer from the gastrointestinal tract and its associated excretory organs will occur in more
than 300,000 Americans in 2017, with colorectal cancer responsible for> 40% of that …

[HTML][HTML] An update on the diagnosis of gastroenteropancreatic neuroendocrine neoplasms

JM Fang, J Li, J Shi - World Journal of Gastroenterology, 2022 - ncbi.nlm.nih.gov
Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) arise from neuroendocrine
cells found throughout the gastrointestinal tract and islet cells of the pancreas. The incidence …

Germline genetic variability in pancreatic cancer risk and prognosis

M Gentiluomo, F Canzian, A Nicolini… - Seminars in cancer …, 2022 - Elsevier
Pancreatic cancer (PC), particularly its most common form, pancreatic ductal
adenocarcinoma (PDAC), is relatively rare but highly lethal. Knowledge about PC risk …

[HTML][HTML] 225Ac-Labeled Somatostatin Analogs in the Management of Neuroendocrine Tumors: From Radiochemistry to Clinic

L Rubira, E Deshayes, L Santoro, PO Kotzki, C Fersing - Pharmaceutics, 2023 - mdpi.com
The widespread use of peptide receptor radionuclide therapy (PRRT) represents a major
therapeutic breakthrough in nuclear medicine, particularly since the introduction of 177Lu …

[HTML][HTML] Novel preclinical gastroenteropancreatic neuroendocrine neoplasia models demonstrate the feasibility of mutation-based targeted therapy

F Viol, B Sipos, M Fahl, TS Clauditz, T Amin, M Kriegs… - Cellular Oncology, 2022 - Springer
Purpose Gastroenteropancreatic neuroendocrine neoplasms (GEP-NEN) form a rare and
remarkably heterogeneous group of tumors. Therefore, establishing personalized therapies …

[HTML][HTML] Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5

AK Giri, M Aavikko, L Wartiovaara, T Lemmetyinen… - Gastroenterology, 2023 - Elsevier
Background & Aims Small intestinal neuroendocrine tumor (SI-NET) is a rare disease, but its
incidence has increased over the past 4 decades. Understanding the genetic risk factors …

IGF2 drives formation of ileal neuroendocrine tumors in patients and mice

T Contractor, R Clausen, GR Harris… - Endocrine-Related …, 2020 - erc.bioscientifica.com
By the strictest of definitions, a genetic driver of tumorigenesis should fulfill two criteria: it
should be altered in a high percentage of patient tumors, and it should also be able to cause …

[HTML][HTML] Molecular subtyping in pancreatic neuroendocrine neoplasms: new insights into clinical, pathological unmet needs and challenges

J Yan, S Yu, C Jia, M Li, J Chen - … et Biophysica Acta (BBA)-Reviews on …, 2020 - Elsevier
Pancreatic neuroendocrine neoplasms (PanNENs) contain two primary subtypes with
distinct molecular features and associated clinical outcomes: well-differentiated …

Clinical implications of pathogenic germline variants in small intestine neuroendocrine tumors (SI-NETs)

K Perez, MH Kulke, A Chittenden, C Ukaegbu… - JCO Precision …, 2021 - ascopubs.org
PURPOSE An inherited basis for presumed sporadic neuroendocrine tumor (NET) has been
suggested by evidence of familial clustering of NET and a higher incidence of second …

[HTML][HTML] Clinical features, management, and molecular characteristics of familial small bowel neuroendocrine tumors

JY Lim, RF Pommier - Frontiers in Endocrinology, 2021 - frontiersin.org
Small bowel neuroendocrine tumors are rare tumors with an increasing incidence over the
last several decades. Early detection remains challenging because patients commonly …