TY - JOUR
T1 - Microsatellite instability in japanese esophageal carcinoma
AU - Nakashima, Hideaki
AU - Mori, Masaki
AU - Mimori, Koshi
AU - Inoue, Hiroshi
AU - Shibuta, Kenji
AU - Baba, Kinva
AU - Mafune, Ken‐Ichi ‐I
AU - Akiyoshi, Tsuyoshi
PY - 1995/8/22
Y1 - 1995/8/22
N2 - Recent studies have shown that microsatellite instability (MSI) may play an important role in the development of various types of cancer. However, there have been only 2 reports describing MSI in esophageal carcinoma and the clinicopathologic significance of MSI in this malignancy has not yet been clarified. To better elucidate the role of genetic instability in the development of esophageal carcinoma, we investigated the presence of MSI in 32 cases of esophageal cancer using paired samples of fresh frozen tumor and normal tissue by a method based on the polymerase chain reaction. MSI was defined as occurring in tumors which showed altered banding patterns at one or more microsatellite loci. The incidence of MSI in esophageal carcinoma was 6 out of 32 patients. MSI was observed more frequently in cases with small‐cell carcinoma (2 out of 2) than in cases with squamous‐cell carcinoma (4 out of 29). No cases with adenocarcinoma or Barrett's metaplasia were included in our series. No significant correlations between MSI and other clinicopathologic parameters were observed. The present study suggests that (I) some Japanese esophageal carcinomas certainly correlate with DNA replication error, and (2) MSI may be more frequent in small‐cell carcinoma of the esophagus than in squamous‐cell carcinoma of the esophagus. © 1995 Wiley‐Liss, Inc.
AB - Recent studies have shown that microsatellite instability (MSI) may play an important role in the development of various types of cancer. However, there have been only 2 reports describing MSI in esophageal carcinoma and the clinicopathologic significance of MSI in this malignancy has not yet been clarified. To better elucidate the role of genetic instability in the development of esophageal carcinoma, we investigated the presence of MSI in 32 cases of esophageal cancer using paired samples of fresh frozen tumor and normal tissue by a method based on the polymerase chain reaction. MSI was defined as occurring in tumors which showed altered banding patterns at one or more microsatellite loci. The incidence of MSI in esophageal carcinoma was 6 out of 32 patients. MSI was observed more frequently in cases with small‐cell carcinoma (2 out of 2) than in cases with squamous‐cell carcinoma (4 out of 29). No cases with adenocarcinoma or Barrett's metaplasia were included in our series. No significant correlations between MSI and other clinicopathologic parameters were observed. The present study suggests that (I) some Japanese esophageal carcinomas certainly correlate with DNA replication error, and (2) MSI may be more frequent in small‐cell carcinoma of the esophagus than in squamous‐cell carcinoma of the esophagus. © 1995 Wiley‐Liss, Inc.
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U2 - 10.1002/ijc.2910640413
DO - 10.1002/ijc.2910640413
M3 - Article
C2 - 7657394
AN - SCOPUS:0029129446
SN - 0020-7136
VL - 64
SP - 286
EP - 289
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 4
ER -