Jang Tae Jung, Ji Ye Seob, Jung Ki Hoon
Department of Pathology, Dongguk University College of Medicine, 707 Sukjang-dong, Kyongju, Kyongbuk 780-714, Korea.
Yonsei Med J. 2008 Dec 31;49(6):917-22. doi: 10.3349/ymj.2008.49.6.917.
Gastric carcinoma tissues release high level of prostaglandin E2 (PGE2) when compared to non-neoplastic mucosa, and cyclooxygenase-2 (COX-2), which is the rate-limiting enzyme in prostaglandin (PG) biosynthesis, is often overexpressed in gastric carcinomas and during gastric carcinogenesis. However, little is known about the expression of 15-hydroxyprostaglandin dehydrogenase (15-PGDH), the key enzyme responsible for the biological inactivation of PG, in gastric carcinomas.
We investigated the expression of 15-PGDH in 28 cases of advanced gastric carcinomas by Western blot analysis and also the relation between its expression and the gene promoter methylation.
15-PGDH expression was significantly decreased in gastric carcinomas compared to corresponding non-neoplastic tissues and inversely correlated with the expression of proliferating cell nuclear antigen in gastric carcinomas. However, there was no correlation between 15-PGDH expression and pathological findings such as nodal metastasis and vascular invasion. Promoter hypermethylation of 15-PGDH gene was not detected in carcinomas, with only a negligible expression of the enzyme.
Our results suggested that 15-PGDH has tumor suppressor activity in gastric carcinomas.
与非肿瘤性黏膜相比,胃癌组织释放高水平的前列腺素E2(PGE2),且环氧化酶-2(COX-2)作为前列腺素(PG)生物合成中的限速酶,在胃癌及胃癌发生过程中常过度表达。然而,关于15-羟基前列腺素脱氢酶(15-PGDH)这一负责PG生物失活的关键酶在胃癌中的表达情况,人们了解甚少。
我们通过蛋白质印迹分析研究了28例进展期胃癌中15-PGDH的表达情况,并探讨了其表达与基因启动子甲基化之间的关系。
与相应的非肿瘤组织相比,胃癌中15-PGDH的表达显著降低,且与胃癌中增殖细胞核抗原的表达呈负相关。然而,15-PGDH的表达与诸如淋巴结转移和血管侵犯等病理结果之间并无关联。在癌组织中未检测到15-PGDH基因的启动子高甲基化,该酶的表达仅可忽略不计。
我们的结果表明,15-PGDH在胃癌中具有肿瘤抑制活性。