Literature DB >> 16328596

Relationship between biological behavior and phenotypic expression in undifferentiated-type gastric carcinomas.

Akira Kabashima1, Takashi Yao, Yoshihiko Maehara, Masazumi Tsuneyoshi.   

Abstract

BACKGROUND: It has been proved that some differentiated-type gastric carcinomas have a gastric phenotype. Similarly, it can be conjectured that some undifferentiated-type gastric carcinomas have an intestinal phenotype and that there are biological differences between undifferentiated-type gastric carcinomas with a gastric phenotype and those with an intestinal phenotype. We classified the phenotypes of early undifferentiated-type gastric carcinomas and investigated the relationship between their biological behavior and the phenotypes.
METHODS: Sixty lesions of intramucosal undifferentiated-type gastric carcinoma were classified into four phenotypes; gastric type, incomplete-intestinal type, complete-intestinal type, and unclassified type, according to the expression of CD10, MUC2, small-intestinal mucinous antigen (SIMA), human gastric mucin (HGM), or concanavalin A (ConA).
RESULTS: The incidence of gastric-type carcinoma, incomplete-intestinal-type carcinoma, and complete-intestinal-type carcinoma was 33% (20 cases), 65% (39 cases), and 2% (1 case), respectively. There was no significant difference in any of the clinicopathological factors examined between the 20 gastric-type carcinomas and the 40 intestinal-type carcinomas, but there were significant differences in the morphological findings. Intestinal-type carcinomas had a glandular structure more frequently than the gastric-type carcinomas. The spreading pattern of gastric-type carcinomas showed a middle-layer type more frequently than the intestinal-type carcinomas.
CONCLUSION: Undifferentiated-type gastric carcinomas frequently expressed an intestinal phenotype. There were differences in the growth patterns between undifferentiated-type gastric carcinomas with a gastric phenotype and those with the intestinal phenotype.

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Year:  2005        PMID: 16328596     DOI: 10.1007/s10120-005-0340-9

Source DB:  PubMed          Journal:  Gastric Cancer        ISSN: 1436-3291            Impact factor:   7.370


  28 in total

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Journal:  World J Gastroenterol       Date:  2010-10-07       Impact factor: 5.742

3.  Re-evaluation of phenotypic expression in undifferentiated-type early gastric adenocarcinomas using mucin core protein and CDX2.

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Journal:  Gastric Cancer       Date:  2012-07-25       Impact factor: 7.370

4.  Can we resect EGC with Signet ring cells in Europe?

Authors:  Fabrice Caillol; Erwan Bories; Jerôme Guiramand; Christian Pesenti; Florat Poizat; Geneviève Monges; Marc Giovannini
Journal:  J Gastrointest Cancer       Date:  2013-12

5.  The nature of the white opaque substance within colorectal neoplastic epithelium as visualized by magnifying endoscopy with narrow-band imaging.

Authors:  Kentaro Imamura; Kenshi Yao; Takashi Hisabe; Masami Nambu; Kensei Ohtsu; Tetsuya Ueo; Shinji Yano; Hiroshi Ishihara; Takashi Nagahama; Takao Kanemitsu; Kazutomo Yamasaki; Toshiyuki Matsui; Hiroshi Tanabe; Akinori Iwashita; Tsutomu Daa; Shigeo Yokoyama; Kazuhisa Matsunaga; Munechika Enjoji
Journal:  Endosc Int Open       Date:  2016-10-20
  5 in total

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