Browse > Article
http://dx.doi.org/10.5230/jgc.2010.10.4.149

Microsatellite Instability Is Associated with the Clinicopathologic Features of Gastric Cancer in Sporadic Gastric Cancer Patients  

Kim, Shin-Hyuk (Department of Surgery, Hanyang University College of Medicine)
Ahn, Byung-Kyu (Department of Surgery, Hanyang University College of Medicine)
Nam, Young-Su (Department of Surgery, Hanyang University College of Medicine)
Pyo, Joo-Youn (Department of Pathology, Hanyang University College of Medicine)
Oh, Young-Ha (Department of Pathology, Hanyang University College of Medicine)
Lee, Kang-Hong (Department of Surgery, Hanyang University College of Medicine)
Publication Information
Journal of Gastric Cancer / v.10, no.4, 2010 , pp. 149-154 More about this Journal
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.
Keywords
Microsatellite instability; Stomach neoplasms; Synchronous gastric cancer;
Citations & Related Records
Times Cited By KSCI : 3  (Citation Analysis)
연도 인용수 순위
1 Lynch HT, Smyrk TC, Watson P, Lanspa SJ, Lynch JF, Lynch PM, et al. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review. Gastroenterology 1993;104:1535-1549.   DOI
2 Japanese Gastric Cancer Association. Japanese classifi cation of gastric carcinoma - 2nd english edition -. Gastric Cancer 1998;1:10-24.   DOI
3 Sepulveda AR, Santos AC, Yamaoka Y, Wu L, Gutierrez O, Kim JG, et al. Marked diff erences in the frequency of microsatellite instability in gastric cancer from diff erent countries. Am J Gastroenterol 1999;94:3034-3038.   DOI   ScienceOn
4 Lim S, Lee HS, Kim HS, Kim YI, Kim WH. Alteration of Ecadherin-mediated adhesion protein is common, but microsatellite instability is uncommon in young age gastric cancers. Histopathology 2003;42:128-136.   DOI   ScienceOn
5 Hayden JD, Cawkwell L, Quirke P, Dixon MF, Goldstone AR, Sue-Ling H, et al. Prognostic significance of microsatellite instability in patients with gastric carcinoma. Eur J Cancer 1997;33:2342-2346.   DOI   ScienceOn
6 Nakashima H, Inoue H, Honda M, Shibuta K, Arinaga S, Mori M, et al. Th e heterogeneity of microsatellite instability in multiple gastric cancers. Am J Gastroenterol 1995;90:653-656.
7 Oliveira C, Seruca R, Seixas M, Sobrinho-Simoes M. The clinicopathological features of gastric carcinomas with microsatellite instability may be mediated by mutations of diff erent "target genes": a study of the TGFbeta RII, IGFII R, and BAX genes. Am J Pathol 1998;153:1211-1219.   DOI
8 Miyoshi E, Haruma K, Hiyama T, Tanaka S, Yoshihara M, Shimamoto F, et al. Microsatellite instability is a genetic marker for the development of multiple gastric cancers. Int J Cancer 2001;95:350-353.   DOI   ScienceOn
9 Kodera Y, Yamamura Y, Torii A, Uesaka K, Hirai T, Yasui K, et al. Incidence, diagnosis and signifi cance of multiple gastric cancer. Br J Surg 1995;82:1540-1543.   DOI   ScienceOn
10 Kim HC, Roh SA, Yook JH, Oh ST, Kim BS, Yu CS, et al. Microsatellite instability and promoter methylation of hMLH1 in sporadic gastric carcinoma. J Korean Gastric Cancer Assoc 2003;3:50-55.   과학기술학회마을   DOI
11 Lauren P. The two histological main types of gastric carcinoma: diffuse and so-called intestinal-type carcinoma. An attempt at a HISTO-clinical classifi cation. Acta Pathol Microbiol Scand 1965;64:31-49.   DOI
12 Cleary JB, Kazarian KK, Mersheimer WL. Multiple primary cancer. Th irty patients with three or more primary cancers. Am J Surg 1975;129:686-690.   DOI   ScienceOn
13 Suraweera N, Duval A, Reperant M, Vaury C, Furlan D, Leroy K, et al. Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR. Gastroenterology 2002;123:1804-1811.   DOI   ScienceOn
14 Boland CR, Th ibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998;58:5248-5257.
15 Ahn YJ, Oh SJ, Song JW, Kang WH, Hyung WJ, Choi SH, et al. The clinicopathologic features and prognosis of multiple early gastric cancer. J Korean Gastric Cancer Assoc 2008;8:198-203.   과학기술학회마을   DOI
16 Ribeiro U Jr, Jorge UM, Safatle-Ribeiro AV, Yagi OK, Scapulatempo C, Perez RO, et al. Clinicopathologic and immunohistochemistry characterization of synchronous multiple primary gastric adenocarcinoma. J Gastrointest Surg 2007;11:233-239.   DOI   ScienceOn
17 Bae JS, Lee JH, Ryu KW, Kim YW, Bae JM. Characteristics of synchronous cancers in gastric cancer patients. Cancer Res Treat 2006;38:25-29.   DOI   ScienceOn
18 Tahara E. Molecular mechanism of stomach carcinogenesis. J Cancer Res Clin Oncol 1993;119:265-272.   DOI
19 Chong JM, Fukayama M, Hayashi Y, Takizawa T, Koike M, Konishi M, et al. Microsatellite instability in the progression of gastric carcinoma. Cancer Res 1994;54:4595-4597.
20 Pedroni M, Tamassia MG, Percesepe A, Roncucci L, Benatti P, Lanza G Jr, et al. Microsatellite instability in multiple colorectal tumors. Int J Cancer 1999;81:1-5.   DOI   ScienceOn
21 Sengupta SB, Yiu CY, Boulos PB, De Silva M, Sams VR, Delhanty JD. Genetic instability in patients with metachronous colorectal cancers. Br J Surg 1997;84:996-1000.   DOI   ScienceOn
22 Bae JM, Won YJ, Jung KW, Suh KA, Ahn DH, Park JG. Annual report of the central cancer registry in Korea-1999: based on registered data from 128 hospitals. Cancer Res Treat 2001;33:367-372.   DOI
23 Honmyo U, Misumi A, Murakami A, Haga Y, Akagi M. Clinicopathological analysis of synchronous multiple gastric carcinoma. Eur J Surg Oncol 1989;15:316-321.
24 Kaibara N, Maeta M, Ikeguchi M. Patients with multiple primary gastric cancers tend to develop second primaries in organs other than the stomach. Surg Today 1993;23:186-188.   DOI   ScienceOn