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Approach to the mechanism of invasion and metastasis in oral squamous cell carcinoma from sphingolipid.

Research Project

Project/Area Number 26670875
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Surgical dentistry
Research InstitutionKanazawa Medical University

Principal Investigator

KATO Koichiro  金沢医科大学, 医学部, 助教 (30719373)

Co-Investigator(Kenkyū-buntansha) UEDA Yoshimichi  金沢医科大学, 医学部, 教授 (50271375)
Co-Investigator(Renkei-kenkyūsha) OKAZAKI Toshiro  金沢医科大学, 医学部, 教授 (40233308)
Project Period (FY) 2014-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords口腔扁平上皮癌 / 浸潤性増殖
Outline of Final Research Achievements

Sphingosin kinase 1 is expressed in the invading squamous cell carcinoma (SCC) cells of the oral cavity. Expression of sphingosin kinase 1 is not related to the differentiation of the tumor cells. Sphingosin kinase 1 is not associated with proliferative activity of SCC of the oral cavity but epithelial-mesenchymal transition (EMT) of SCC cells. It is suggested that Grade 3 and 4C SCC cells require tumor cell-host cell interaction to upregulate SK1, and Grade 4D cells are not dependent on the interaction but able to upregulate SK1 by themselves and exhibit vigorous invading capability.

Report

(3 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report

URL: 

Published: 2014-04-04   Modified: 2017-05-10  

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