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Distinct expression profile of key molecules in crawling-type early gastric carcinoma

Authors
 Ha Young Woo  ;  Yoon Sung Bae  ;  Jie-Hyun Kim  ;  Sang Kil Lee  ;  Yong Chan Lee  ;  Jae-Ho Cheong  ;  Sung Hoon Noh  ;  Hyunki Kim 
Citation
 Gastric Cancer, Vol.20(4) : 612-619, 2017 
Journal Title
 Gastric Cancer 
ISSN
 1436-3291 
Issue Date
2017
MeSH
Adenocarcinoma/pathology* ; Adult ; Aged ; Biomarkers, Tumor/analysis* ; Female ; Humans ; Male ; Middle Aged ; Stomach Neoplasms/pathology* ; Transcriptome
Keywords
Crawling-type adenocarcinoma ; Gastric cancer ; Protein expression profile
Abstract
BACKGROUND: Gastric "crawling-type" adenocarcinoma (CRA) is a tumor histologically characterized by irregularly fused glands with low-grade cellular atypia that tends to spread laterally in the mucosa. To date, the expression characteristics of the key molecules involved in CRA, including receptor tyrosine kinases (RTKs), mismatch repair (MMR) proteins, phosphatase and tensin homolog (PTEN), as well as the Epstein-Barr virus (EBV) status, have yet to be uncovered. METHODS: We constructed tissue microarrays of 94 CRAs, 72 conventional-type differentiated adenocarcinomas (CDAs), and 71 intramucosal poorly cohesive adenocarcinomas (PCAs) from early gastric cancers to evaluate and compare the pathological and expression profiles of potential key molecules for molecular classification (EBV; four MMR proteins-MLH1, MSH2, PMS2, and MSH6; three RTKs-HER2, MET, and EGFR; PTEN; and p53). RESULTS: None of the CRAs showed MMR deficiency (0.0 % vs. 5.6 %, CRA vs. CDA, p = 0.036), HER2 overexpression (0.0 % vs. 12.5 %, p = 0.001), or loss of PTEN expression (0.0 % vs. 9.7 %, p = 0.003). Moreover, MET overexpression (4.4 % vs. 19.4 %, p = 0.004), and a mutant p53 pattern (12.4 % vs. 62.5 %, p < 0.001) were significantly less common in CRAs than in CDAs. However, clinicopathological features and all the profile of the molecules of CRAs were close to those of the PCA group. CONCLUSIONS: CRA demonstrated unique clinicopathological characteristics and showed a distinct expression profile of key molecules, which was close to that of a null phenotype. These results support the classification of CRA as a distinct subgroup of gastric adenocarcinoma.
Full Text
https://link.springer.com/article/10.1007%2Fs10120-016-0652-y
DOI
10.1007/s10120-016-0652-y
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Jie-Hyun(김지현) ORCID logo https://orcid.org/0000-0002-9198-3326
Kim, Hyunki(김현기) ORCID logo https://orcid.org/0000-0003-2292-5584
Noh, Sung Hoon(노성훈) ORCID logo https://orcid.org/0000-0003-4386-6886
Bae, Yoon Sung(배윤성)
Woo, Ha Young(우하영) ORCID logo https://orcid.org/0000-0002-3078-6484
Lee, Sang Kil(이상길) ORCID logo https://orcid.org/0000-0002-0721-0364
Lee, Yong Chan(이용찬) ORCID logo https://orcid.org/0000-0001-8800-6906
Cheong, Jae Ho(정재호) ORCID logo https://orcid.org/0000-0002-1703-1781
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URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/161092
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