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Relationship between 15-hydroxyprostaglandin dehydrogenase and gastric adenocarcinoma
Annals of Surgical Treatment and Research ; : 302-308, 2014.
Article in English | WPRIM | ID: wpr-152271
ABSTRACT

PURPOSE:

Prostaglandin E2 (PGE2) is a contributory carcinogen in gastric adenocarcinoma. 15-Hydroxyprostaglandin dehydrogenase (15-PGDH) catabolizes PGE2 by oxidizing its 15(s)-hydroxy group. The aim of this study was to investigate the expression of 15-PGDH in gastric adenocarcinoma tissue and the relationship between 15-PGDH expression and clinicopathologic features of gastric adenocarcinoma.

METHODS:

Ninety-nine patients who underwent surgical resection for gastric adenocarcinoma between January 2007 and December 2007 were enrolled and evaluated retrospectively.

RESULTS:

In 62 patients (62.6%), 15-PGDH expression was lower in gastric adenocarcinoma tissue than in nonneoplastic tissue. Regarding the relationship between 15-PGDH expression and clinicopathological features, 15-PGDH expression was significantly lower in tissues with poor differentiation (P = 0.002), advanced T stage (P = 0.0319), a higher number of lymph node metastases (P = 0.045), lymphatic invasion (P = 0.031), and vascular invasion (P = 0.036).

CONCLUSION:

15-PGDH expression was associated with a subset of clinicopathologic features such as differentiation grade, T stage, lymphatic invasion, and vascular invasion.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Oxidoreductases / Stomach Neoplasms / Dinoprostone / Adenocarcinoma / Retrospective Studies / Lymph Nodes / Neoplasm Metastasis Type of study: Observational study Limits: Humans Language: English Journal: Annals of Surgical Treatment and Research Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Oxidoreductases / Stomach Neoplasms / Dinoprostone / Adenocarcinoma / Retrospective Studies / Lymph Nodes / Neoplasm Metastasis Type of study: Observational study Limits: Humans Language: English Journal: Annals of Surgical Treatment and Research Year: 2014 Type: Article