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Elucidation of interaction between of LINC complex with adhesion molecule

Research Project

Project/Area Number 24659162
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeSingle-year Grants
Research Field Human pathology
Research InstitutionOsaka University

Principal Investigator

HAMADA Yoshinosuke  大阪大学, 医学(系)研究科(研究院), 助教 (10362683)

Co-Investigator(Kenkyū-buntansha) MATSUURA Nariaki  大阪大学, 大学院医学系研究科, 教授 (70190402)
KAWAGUCHI Naomasa  大阪大学, 大学院医学系研究科, 准教授 (70224748)
MORI Seizi  大阪大学, 大学院医学系研究科, 助教 (90467506)
Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
KeywordsLINC complex / nesprin / laminA/C / SUN1 / SUN2 / nesprin2 / 分子病理
Research Abstract

The evaluation of mRNA and protein expression by cellular experiments revealed a decrease in the expression of SUN2 and nesprin 2, and the evaluation of the expression of these proteins by immunostaining of tissue samples revealed a tendency for a decrease in the expression of lamin A/C, SUN1, SUN2, and nesprin 2. Furthermore, results of the statistical analysis showed that lamin A/C and nesprin 2 contributed to the exacerbation of breast cancer. Previous cellular-level studies have also reported the existence of a relationship between decreased lamin A/C expression and the exacerbation of breast cancer. These evidences suggest that the expression of LINC complex proteins tends to be decreased in patients with breast cancer and that a decreased expression of lamin A/C and nesprin 2, in particular, is involved in the exacerbation of breast cancer.

Report

(3 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • Research Products

    (1 results)

All 2013

All Journal Article (1 results) (of which Peer Reviewed: 1 results)

  • [Journal Article] A dominant-negative FGF1 mutant (the R50E mutant) suppresses tumorigenesis and angiogenesis.2013

    • Author(s)
      Mori S, Tran V, Nishikawa K, Kaneda T, Hamada Y, Kawaguchi N, Fujita M, Takada YK, Matsuura N, Zhao M, Takada Y.
    • Journal Title

      PLoS One.

      Volume: 8

    • Related Report
      2013 Annual Research Report
    • Peer Reviewed

URL: 

Published: 2013-05-31   Modified: 2019-07-29  

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