Three Molecular Subtypes of Gastric Adenocarcinoma Have Distinct Histochemical Features Reflecting Epstein-Barr Virus Infection Status and Neuroendocrine Differentiation
Year: 2014
Type: article
Study design: Observational Study
Abstract: Current histopathologic classification schemes for gastric adenocarcinoma have limited clinical utility and are difficult to apply due to tumor heterogeneity. Elucidation of molecular subtypes of gastric cancer may contribute to our understanding of gastric cancer biology and to the development of new molecular markers that may lead to improved diagnosis, therapy, or prognosis. We previously demonstrated that Epstein-Barr virus (EBV)-infected gastric cancers have a distinct human gene expression profile compared with uninfected cancers. We now examine the histopathologic features characterizing infected (n=14) and uninfected (n=89) cancers; the latter of which are now further divided into 2 major molecular subtypes based on expression patterns of 93 RNAs. One uninfected gastric cancer subtype was distinguished by upregulation of 3 genes with neuroendocrine (NE) function (CHGA, GAST, and REG4 encoding chromogranin, gastrin, and the secreted peptide REG4 involved in epithelial cell regeneration), implicating hormonal factors in the pathogenesis of a major class of gastric adenocarcinomas. Evidence of NE differentiation (molecular, immunohistochemical, or morphologic) was mutually exclusive of EBV infection. EBV-infected tumors tended to have solid-type morphology with lymphoid stroma. This study reveals novel molecular subtypes of gastric cancer and their associated morphologies that demonstrate divergent NE features.
Authors: Olga Speck, Weihua Tang, Douglas R. Morgan, Pei Fen Kuan, Michael O. Meyers, Ricardo L. Dominguez, Enrique Martinez, Margaret L. Gulley
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: G2056852899, G206438753, Etiological Studies of Gastric Carcinoma, North Carolina Translational & Clinical Sciences Institute (NC TraCS), Network Group Integrated Translational Science Centers Application, Targeted chemoprevention of gastric carcinogenesis in high risk populations, G5950577451, Cancer and Leukemia Group B, G6741197049, Enhanced Formalin Fixation to Improve Tests on Solid Tissues, Gastric Cancer Epidemiology Initiative in Central America
OpenAlex ID: W2316530024
