Relationship between biological behavior and phenotypic expression in undifferentiated-type gastric carcinomas
- PMID: 16328596
- DOI: 10.1007/s10120-005-0340-9
Relationship between biological behavior and phenotypic expression in undifferentiated-type gastric carcinomas
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.
Similar articles
-
Re-evaluation of mucin phenotypes of gastric minute well-differentiated-type adenocarcinomas using a series of HGM, MUC5AC, MUC6, M-GGMC, MUC2 and CD10 stains.Pathol Int. 2004 May;54(5):311-21. doi: 10.1111/j.1440-1827.2004.01625.x. Pathol Int. 2004. PMID: 15086835
-
Gastric and intestinal phenotypic marker expression in gastric carcinomas and its prognostic significance: immunohistochemical analysis of 136 lesions.Oncology. 2001;61(3):212-20. doi: 10.1159/000055377. Oncology. 2001. PMID: 11574777
-
Mucin phenotype and background mucosa of intramucosal differentiated-type adenocarcinoma of the stomach.Oncology. 2004;66(5):379-87. doi: 10.1159/000079486. Oncology. 2004. PMID: 15331925
-
[Gastric differentiated stomach adenocarcinoma].Pathologe. 2001 Mar;22(2):97-104. doi: 10.1007/s002920000444. Pathologe. 2001. PMID: 11321735 Review. German.
-
The challenge of undifferentiated malignancies: Phenotype versus genotype! What matters most?Semin Diagn Pathol. 2021 Nov;38(6):117-118. doi: 10.1053/j.semdp.2021.09.002. Epub 2021 Sep 20. Semin Diagn Pathol. 2021. PMID: 34556375 Review. No abstract available.
Cited by
-
Re-evaluation of phenotypic expression in undifferentiated-type early gastric adenocarcinomas using mucin core protein and CDX2.Gastric Cancer. 2013 Apr;16(2):208-19. doi: 10.1007/s10120-012-0172-3. Epub 2012 Jul 25. Gastric Cancer. 2013. PMID: 22829163
-
Mucin phenotype of gastric cancer and clinicopathology of gastric-type differentiated adenocarcinoma.World J Gastroenterol. 2010 Oct 7;16(37):4634-9. doi: 10.3748/wjg.v16.i37.4634. World J Gastroenterol. 2010. PMID: 20872962 Free PMC article.
-
Can we resect EGC with Signet ring cells in Europe?J Gastrointest Cancer. 2013 Dec;44(4):422-7. doi: 10.1007/s12029-013-9529-z. J Gastrointest Cancer. 2013. PMID: 23912607
-
Relationship between clinicopathological features and mucin phenotypes of advanced gastric adenocarcinoma.World J Gastroenterol. 2010 Jun 14;16(22):2764-70. doi: 10.3748/wjg.v16.i22.2764. World J Gastroenterol. 2010. PMID: 20533596 Free PMC article.
-
The nature of the white opaque substance within colorectal neoplastic epithelium as visualized by magnifying endoscopy with narrow-band imaging.Endosc Int Open. 2016 Nov;4(11):E1151-E1157. doi: 10.1055/s-0042-116487. Epub 2016 Oct 20. Endosc Int Open. 2016. PMID: 27853741 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous