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Modern Management of Gastric Neuroendocrine Neoplasms.

Curr Treat Options Oncol

September 2024

Department of Medicine, Section of Medical Oncology, Yale School of Medicine, 25 York Street, New Haven, CT, 06510, USA.

Gastric neuroendocrine neoplasms (G-NENs) are a heterogeneous group of tumors that broadly fall into two groups. The first group, driven by oversecretion of gastrin, are generally multifocal, small, and behave indolently with a low (but non-zero) risk of progression and metastatic spread. They are conventionally categorized into type 1, with endogenous gastric-based overproduction of gastrin, and type 2 G-NEN, with overproduction of gastrin from an extra-gastric gastrin-secreting tumor.

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Article Synopsis
  • Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are complex cancers influenced by the interaction of tumor cells with their surrounding microenvironment, necessitating the study of tumor-derived signals.
  • Researchers utilized digital spatial profiling (DSP) to analyze the expression of immune and neural proteins in a variety of GEP-NETs, demonstrating that immune-related proteins may facilitate neuroendocrine differentiation and tumor growth.
  • The findings indicated notable differences between gastrin-secreting and non-functional NETs, particularly in protein expression and immune cell presence, with MEN1-related tumors showing strong immune exclusion and unique neuro-immune signatures.
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Zollinger-Ellison syndrome (ZES) is a distinct syndrome characterized by hyperchlorhydria-induced peptic ulcer disease and chronic diarrhea. It is the result of a gastrin-excess state caused by a duodenal or pancreatic neuroendocrine tumor referred to as gastrinoma. This gastrin-secreting neuroendocrine tumor is usually sporadic in nature, or part of multiple endocrine neoplasia type 1 syndrome.

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