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Microsatellite instability is associated with the clinicopathologic features of gastric cancer in sporadic gastric cancer patientsopen access

Authors
Kim, Shin HyukAhn, Byung KyuNam, Young SuPyo, Joo YounOh, Young HaLee, Kang Hong
Issue Date
Dec-2010
Publisher
The Korean Gastric Cancer Association
Keywords
Microsatellite instability; Stomach neoplasms; Synchronous gastric cancer
Citation
Journal of Gastric Cancer, v.10, no.4, pp.149 - 154
Indexed
SCOPUS
KCI
OTHER
Journal Title
Journal of Gastric Cancer
Volume
10
Number
4
Start Page
149
End Page
154
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/173349
DOI
10.5230/jgc.2010.10.4.149
ISSN
2093-582X
Abstract
Purpose: Replication error is an important mechanism in carcinogenesis. The microsatellite instability (MSI-H) of colorectal cancers is associated with the development of multiple cancers. The influence of MSI-H on the development of multiple gastric cancers in sporadic gastric cancer patients has not been defined. This study was performed to reveal the association between the clinicopathologic features and MSI in sporadic gastric cancers. Materials and Methods: Between July 2004 and March 2009, the clinicopathologic characteristics, including MSI status, were evaluated in 128 consecutive patients with sporadic gastric cancers. None of the patients had hereditary non-polyposis colorectal cancer of familial gastric cancer. The markers that were recommended by the NCI to determine the MSI status for colorectal cancers were used. Results: MSI-H cancers were found in 10.9% of the patients (14/128). Synchronous gastric cancers were shown in 4 patients (3.1%). Synchronous cancers were found in 2 of 14 patients with MSI-H gastric cancer (14.3%) and 2 of 114 patients with MSS gastric cancer (1.8%; P=0.059, Fisher's exact test). Among the patients with synchronous cancer 50% (2/4) had MSI-H cancer, but 9.7% of the patients (12/124) without synchronous cancer had MSI-H cancer. MSI-H (RR, 24.7; 95% CI, 1.5~398.9; P=0.024) was related with to synchronous gastric cancer, but age, gender, family history, histologic type, location, gross morphology, size, and stage were not related to synchronous gastric cancer. Conclusions: MSI is associated with the intestinal-type gastric cancer and the presence of multiple gastric cancers in patients with sporadic gastric cancer. Special attention to the presence of synchronous and the development of metachronous multiple cancer in patients with MSI-H gastric cancer is needed.
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