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Basic study on anti-tumor activity of non-vitamin K dependent oral anticoagulants (NOACs)

Research Project

Project/Area Number 16K08633
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Pathological medical chemistry
Research InstitutionSuzuka University of Medical Science

Principal Investigator

SUZUKI Koji  鈴鹿医療科学大学, 薬学部, 教授 (70077808)

Research Collaborator HIRAMOTO Keiichi  
HAYASHI Tatsuya  
OKAMOTO Takayuki  
NISHIOKA Junji  
AKITA Nobuyuki  
TERASAWA Masahiro  
Project Period (FY) 2016-04-01 – 2019-03-31
Project Status Completed (Fiscal Year 2018)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2018: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2016: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Keywords抗凝固薬 / NOACs / Xa因子阻害薬 / Xa因子受容体 / 抗腫瘍作用 / 抗転移作用 / 大腸癌細胞 / メラノーマ細胞 / 癌 / 薬学 / 病理学 / 細胞・組織 / 酵素
Outline of Final Research Achievements

Non-vitamin K-dependent oral anticoagulants (NOACs) are used as preventives for cerebral thromboembolism and deep vein thrombosis in the lower limbs. In this study, we analyzed the antitumor effects of NOACs. Anti-thrombin drug (drug A) and anti-Xa drug (drug B, drug C) are orally administered daily to tumor-bearing mice to which colon cancer cells Colon-26 cells have been transplanted, and blood and tumor tissue obtained from mice on day 21 were collected and analyzed. As a result, drug B dose-dependently suppressed the growth of tumor cells, the expression of IL-6 and MMP-2 in blood, the expression of cell membrane factor Xa receptor of tumor tissue, and the expression of cell division related factors. It also promoted apoptosis of tumor cells. In addition, drug B suppressed metastasis of melanoma cells to the lung, liver and other organs.

Academic Significance and Societal Importance of the Research Achievements

現在、癌患者数は増加の一途にあり、これまでにない新しい視点からの癌の発生や増殖・転移阻止の方策の確立が求められている。私はこれまでの血栓止血学研究の経験から、血液の流動性維持に重要な凝固制御系因子が癌細胞の増殖や転移を抑制する可能性を示してきた。そこで本研究では、癌細胞の増殖と転移に及ぼす経口抗凝固薬NOACsの影響とその作用機序を解析し、NOACsが癌細胞の増殖と転移を抑制することを示し、その作用機序の一端を明らかにすることができた。こうした研究はこれまで国内外で殆ど行われておらず、得られた成果は独創的で、学術的にも重要であり、癌制御に向けた社会的意義は非常に大きいと考えられる。

Report

(1 results)
  • 2018 Final Research Report ( PDF )

URL: 

Published: 2016-04-21   Modified: 2020-03-30  

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