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Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias

Background and study aims: The authors previously reported that the white opaque substance (WOS) in gastric epithelial neoplasia was caused by accumulation of lipid droplets by immunohistochemical and immunoelectron microscopic studies of adipophilin, which was recently identified and validated as a...

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Autores principales: Ueo, Tetsuya, Yonemasu, Hirotoshi, Yao, Kenshi, Ishida, Tetsuya, Togo, Kazumi, Yanai, Yuka, Fukuda, Masahide, Motomura, Mitsuteru, Narita, Ryoich, Murakami, Kazunari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: © Georg Thieme Verlag KG 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683146/
https://www.ncbi.nlm.nih.gov/pubmed/26716119
http://dx.doi.org/10.1055/s-0034-1393177
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author Ueo, Tetsuya
Yonemasu, Hirotoshi
Yao, Kenshi
Ishida, Tetsuya
Togo, Kazumi
Yanai, Yuka
Fukuda, Masahide
Motomura, Mitsuteru
Narita, Ryoich
Murakami, Kazunari
author_facet Ueo, Tetsuya
Yonemasu, Hirotoshi
Yao, Kenshi
Ishida, Tetsuya
Togo, Kazumi
Yanai, Yuka
Fukuda, Masahide
Motomura, Mitsuteru
Narita, Ryoich
Murakami, Kazunari
author_sort Ueo, Tetsuya
collection PubMed
description Background and study aims: The authors previously reported that the white opaque substance (WOS) in gastric epithelial neoplasia was caused by accumulation of lipid droplets by immunohistochemical and immunoelectron microscopic studies of adipophilin, which was recently identified and validated as a marker of lipid droplets. The aim of the current study was to investigate the characteristics of the histologic differentiation and mucin phenotype in WOS-positive gastric epithelial neoplasias. Patients and methods: A total of 130 gastric epithelial neoplasias (45 adenomas and 85 early adenocarcinomas) from 120 patients were retrospectively evaluated. The presence or absence of WOS was evaluated by M-NBI. Lipids were examined by immunohistochemical staining for adipophilin. Tissue phenotypes were immunohistochemically classified as intestinal (I), gastrointestinal (GI), and gastric (G) using antibodies against CD10, MUC2, MUC5AC and MUC6. The histologic differentiation and mucin phenotype of WOS-positive neoplasias were characterized and examined according to adipophilin expression. Results: The presence of WOS by M-NBI was correlated with histologic differences between adenoma or differentiated type adenocarcinoma and mixed type or undifferentiated type adenocarcinoma (P = 0.0153). Adipophilin was only expressed in primary adenoma and well to moderately differentiated adenocarcinoma components but not in undifferentiated components. WOS and adipophilin expression were only observed in neoplasias with I or GI phenotypes, but not in those with the G phenotype (P < 0.0001). Conclusions: WOS in gastric epithelial neoplasias might indicate differentiation into a mature histological subtype with GI or I mucin phenotype.
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spelling pubmed-46831462015-12-29 Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias Ueo, Tetsuya Yonemasu, Hirotoshi Yao, Kenshi Ishida, Tetsuya Togo, Kazumi Yanai, Yuka Fukuda, Masahide Motomura, Mitsuteru Narita, Ryoich Murakami, Kazunari Endosc Int Open Article Background and study aims: The authors previously reported that the white opaque substance (WOS) in gastric epithelial neoplasia was caused by accumulation of lipid droplets by immunohistochemical and immunoelectron microscopic studies of adipophilin, which was recently identified and validated as a marker of lipid droplets. The aim of the current study was to investigate the characteristics of the histologic differentiation and mucin phenotype in WOS-positive gastric epithelial neoplasias. Patients and methods: A total of 130 gastric epithelial neoplasias (45 adenomas and 85 early adenocarcinomas) from 120 patients were retrospectively evaluated. The presence or absence of WOS was evaluated by M-NBI. Lipids were examined by immunohistochemical staining for adipophilin. Tissue phenotypes were immunohistochemically classified as intestinal (I), gastrointestinal (GI), and gastric (G) using antibodies against CD10, MUC2, MUC5AC and MUC6. The histologic differentiation and mucin phenotype of WOS-positive neoplasias were characterized and examined according to adipophilin expression. Results: The presence of WOS by M-NBI was correlated with histologic differences between adenoma or differentiated type adenocarcinoma and mixed type or undifferentiated type adenocarcinoma (P = 0.0153). Adipophilin was only expressed in primary adenoma and well to moderately differentiated adenocarcinoma components but not in undifferentiated components. WOS and adipophilin expression were only observed in neoplasias with I or GI phenotypes, but not in those with the G phenotype (P < 0.0001). Conclusions: WOS in gastric epithelial neoplasias might indicate differentiation into a mature histological subtype with GI or I mucin phenotype. © Georg Thieme Verlag KG 2015-12 2015-11-05 /pmc/articles/PMC4683146/ /pubmed/26716119 http://dx.doi.org/10.1055/s-0034-1393177 Text en © Thieme Medical Publishers
spellingShingle Article
Ueo, Tetsuya
Yonemasu, Hirotoshi
Yao, Kenshi
Ishida, Tetsuya
Togo, Kazumi
Yanai, Yuka
Fukuda, Masahide
Motomura, Mitsuteru
Narita, Ryoich
Murakami, Kazunari
Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
title Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
title_full Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
title_fullStr Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
title_full_unstemmed Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
title_short Histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
title_sort histologic differentiation and mucin phenotype in white opaque substance-positive gastric neoplasias
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683146/
https://www.ncbi.nlm.nih.gov/pubmed/26716119
http://dx.doi.org/10.1055/s-0034-1393177
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