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2017 Fiscal Year Final Research Report

The molecular mechanism of a lipid mediator involved in metabolic dynamics of breast cancer

Research Project

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Project/Area Number 15K15471
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field General surgery
Research InstitutionNiigata University

Principal Investigator

Nagahashi Masayuki  新潟大学, 医歯学総合病院, 講師 (30743918)

Co-Investigator(Kenkyū-buntansha) 西條 康夫  新潟大学, 医歯学系, 教授 (10270828)
小山 諭  新潟大学, 医歯学系, 教授 (10323966)
小杉 伸一  新潟大学, 医歯学総合病院, 特任教授 (90401736)
小林 隆  新潟大学, 医歯学総合病院, 講師 (40464010)
Project Period (FY) 2015-04-01 – 2018-03-31
Keywords脂質メディエーター / スフィンゴシン-1-リン酸 / スフィンゴシンキナーゼ / 癌代謝 / メタボローム / CRISPR/Cas9
Outline of Final Research Achievements

A pleiotropic bioactive lipid mediator, sphingosine-1-phosphate (S1P), produced by sphingosine kinases (SphK1 and SphK2) regulates many physiological and pathological processes. We hypothesized that SphKs regulates cancer cell-specific metabolism, which related to the cancer cell proliferation and survival. Metabolomics profiles of both SphK1KO and SphK2KO breast cancer cells were dramatically changed in the glycolysis pathway and TCA cycle compared to the control cells. Our data suggests that SphKs play an important role in cancer specific metabolism.

Free Research Field

腫瘍外科

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Published: 2019-03-29  

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