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Reprogramming of hematological malignancies

Research Project

Project/Area Number 21790924
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Hematology
Research InstitutionKeio University

Principal Investigator

MATSUKI Eri  Keio University, 医学部, 研究員 (80468503)

Project Period (FY) 2009 – 2010
Project Status Completed (Fiscal Year 2010)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2009: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Keywords造血器腫瘍 / リプログラミング
Research Abstract

The current research aimed on identifying the mechanism of transformation of low grade hematological malignancies into a highly aggressive tumor, and to develop novel therapeutics for these types of tumors through reprogramming technology. In order to understand the mechanism of transformation in hematological malignancies, we also focused on a rare subtype of lymphoma called plasmablastic lymphoma, and identified that the aberrant expression of Xbp1(s) led to the transformation into plasmablastic appearance, and that inhibition of Xbp1(s) through a proteasome inhibitor bortezomib harbored a potential for treatment for this type of lymphoma.

Report

(3 results)
  • 2010 Annual Research Report   Final Research Report ( PDF )
  • 2009 Annual Research Report
  • Research Products

    (4 results)

All 2011 2010

All Journal Article (2 results) (of which Peer Reviewed: 2 results) Presentation (2 results)

  • [Journal Article] Identification of loss of p16 expression and upregulation of MDR-1 as genetic events resulting from two novel chromosomal translocations found in a plasmablastic lymphoma of the uterus.2011

    • Author(s)
      Matsuki E, Miyakawa Y, Asakawa S, et al.
    • Journal Title

      Clinical Cancer Research 17巻8号

      Pages: 2101-2112

    • Related Report
      2010 Final Research Report
    • Peer Reviewed
  • [Journal Article] Identification of loss of p16 expression and upregulation of MDR-1 as genetic events resulting from two novel chromosomal translocations found in a plasmablastic lymphoma of the uterus.2011

    • Author(s)
      Matsuki E, Miyakawa Y, Asakawa S, et al.
    • Journal Title

      Clinical Cancer Research

      Volume: 17 Pages: 2101-2109

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Presentation] Establishment of a Novel Cell Line of Plasmablastic Lymphoma with Loss of p16 Tumor Suppressor Protein and Overexpression of MDR.2010

    • Author(s)
      Matsuki E, Miyakawa Y, Asakawa S, et al.
    • Organizer
      52^<nd> Annual Meeting of the American Society of Hematology.
    • Place of Presentation
      Orlando, USA.
    • Related Report
      2010 Final Research Report
  • [Presentation] Establishment of a Novel Cell Line of Plasmablastic Lymphoma with Loss of p16 Tumor Suppressor Protein and Overexpression of MDR2010

    • Author(s)
      Matsuki E, Miyakawa Y, Asakawa S, et al.
    • Organizer
      52^<nd> Annual Meeting of the American Society of Hematology
    • Place of Presentation
      米国、Orlando
    • Related Report
      2010 Annual Research Report

URL: 

Published: 2009-04-01   Modified: 2016-04-21  

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