TY - JOUR
T1 - Nectin1 expression is frequently decreased in gastric cancers
AU - Takahashi, Yu
AU - Yamamichi, Nobutake
AU - Inada, Ken ichi
AU - Shiogama, Kazuya
AU - Sakurai, Kouhei
AU - Takeuchi, Chihiro
AU - Mizutani, Yasuyoshi
AU - Tsutsumi, Yutaka
AU - Koike, Kazuhiko
N1 - Publisher Copyright:
© 2018 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd
PY - 2018/10
Y1 - 2018/10
N2 - Gastric cancer (GC) is rich in many different histological types, but how the histological pattern is defined remains to be proved. The relation between GC histological types and the expression of nectin1, which is one of the cell adhesion molecules that composes adherens junction, has not been reported. According to a publicly available database of 406 GC patients, the median overall survival of Nectin1 high expression patients was 55.4 months and that of low expression patients was 25.6 months (P = 0.0246). Using surgically or endoscopically resected GC samples, nectin1 expression was analyzed by immunohistochemistry. Nectin1 expressed at adherens junction in all the normal epithelial cells. However, nectin1 expressed not at adherens junction but at apical membrane in epithelial cells in intestinal metaplasia. The expression pattern of nectin1 in intestinal type GC resembled to intestinal metaplasia. In order to analyze the difference in nectin1 expression between GC histological types, a total of 116 intestinal type GC and 33 diffuse type GC. The expression of necitin1 in diffuse type GC (3.0%) was remarkably decreased compared to that in intestinal type GC (65.5%) (P < 0.0001). In conclusion, this is the first report showing an association between nectin1 expression and histological subtypes of GC.
AB - Gastric cancer (GC) is rich in many different histological types, but how the histological pattern is defined remains to be proved. The relation between GC histological types and the expression of nectin1, which is one of the cell adhesion molecules that composes adherens junction, has not been reported. According to a publicly available database of 406 GC patients, the median overall survival of Nectin1 high expression patients was 55.4 months and that of low expression patients was 25.6 months (P = 0.0246). Using surgically or endoscopically resected GC samples, nectin1 expression was analyzed by immunohistochemistry. Nectin1 expressed at adherens junction in all the normal epithelial cells. However, nectin1 expressed not at adherens junction but at apical membrane in epithelial cells in intestinal metaplasia. The expression pattern of nectin1 in intestinal type GC resembled to intestinal metaplasia. In order to analyze the difference in nectin1 expression between GC histological types, a total of 116 intestinal type GC and 33 diffuse type GC. The expression of necitin1 in diffuse type GC (3.0%) was remarkably decreased compared to that in intestinal type GC (65.5%) (P < 0.0001). In conclusion, this is the first report showing an association between nectin1 expression and histological subtypes of GC.
UR - http://www.scopus.com/inward/record.url?scp=85053633524&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85053633524&partnerID=8YFLogxK
U2 - 10.1111/pin.12721
DO - 10.1111/pin.12721
M3 - Article
C2 - 30221498
AN - SCOPUS:85053633524
SN - 1320-5463
VL - 68
SP - 557
EP - 562
JO - Pathology International
JF - Pathology International
IS - 10
ER -