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2017 Fiscal Year Final Research Report

The chemoprevention of esophageal carcinogenesis with chronic inflammation by the suppression of lipoxygenase

Research Project

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Project/Area Number 15K10090
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Digestive surgery
Research InstitutionKanazawa University

Principal Investigator

Oyama Katsunobu  金沢大学, 附属病院, 助教 (70460350)

Co-Investigator(Kenkyū-buntansha) 伏田 幸夫  金沢大学, 医学系, 准教授 (10301194)
Project Period (FY) 2015-04-01 – 2018-03-31
Keywords食道発癌 / 炎症発癌 / ラットモデル / LOX
Outline of Final Research Achievements

The incidence of Barrett’s epithelium in control group was 94%, in pranlukast group; 69%, the incidence of esophageal adenocarcinoma in control group; 69%, pranlukast group; 15%. Both of Barrett’s epithelium and esophageal adenocarcinoma generation were significantly suppressed by pranlukast administration. Pranlukast administration suppressed tissue growth activity and increased apoptosis. Infiltrating macrophages were reduced by pranlukast administration.
The administration of pranlukast suppressed the generation of Barrett's epithelium and· esophageal adenocarcinoma. Suppression of chronic inflammatory condition by LOX inhibition lead to suppression of carcinogenesis. Moreover, infiltration of macrophages was particularly suppressed among inflammatory cells. Excessive stimulation of tissue growth by macrophages was considered to be one of carcinogenic factors.

Free Research Field

消化器外科学

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Published: 2019-03-29  

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