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Identification of master regulator on TNBC malignant using TAT protein system

Research Project

Project/Area Number 25893153
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field General surgery
Research InstitutionYamaguchi University

Principal Investigator

WATANABE Kenji  山口大学, 大学研究推進機構, 助教 (50711264)

Research Collaborator MIZUKAMI Yoichi  
URUSHIMA Yutaka  
Project Period (FY) 2013-08-30 – 2015-03-31
Project Status Completed (Fiscal Year 2014)
Budget Amount *help
¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
KeywordsTNBC / TAT protein
Outline of Final Research Achievements

Triple-negative breast cancer (TNBC) is one of breast cancer subtype and often shows more malignant phenotype compared to other subtype of breast cancer. Although there are many reports about TNBC, the master regulator involved in malignancy of TNBC is unclear. In this study, we paid our attentions to TNBC and tried to identify the master regulator involved in proliferation activity of TNBC. To achieve our purpose, we extracted the proteins from TNBC cell line, MDA-MB-231 cells, and fractionated them using ion-exchange chromatography. We transfected the each fractionated proteins into HCC38 cell by TAT system, and measured cell proliferation activity. However, the remarkable change was not detected.

Report

(3 results)
  • 2014 Annual Research Report   Final Research Report ( PDF )
  • 2013 Annual Research Report
  • Research Products

    (1 results)

All 2014

All Presentation (1 results)

  • [Presentation] エイズ侵入タンパク質を用いた乳癌発症因子のハイスループットスクリーニング2014

    • Author(s)
      宇留島裕、泉友則、渡邉健司、濱野公一、水上洋一
    • Organizer
      山口大学生命医工学研究センター開設記念シンポジウム
    • Place of Presentation
      山口大学(山口県宇部市)
    • Year and Date
      2014-12-26
    • Related Report
      2014 Annual Research Report

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Published: 2013-09-12   Modified: 2019-07-29  

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