• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Elucidation of COMMD1 effect in HIV-1 latent infection establishment

Research Project

Project/Area Number 16H07080
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Virology
Research InstitutionKumamoto University

Principal Investigator

Kudo Eriko  熊本大学, エイズ学研究センター, 特定事業研究員 (00779176)

Project Period (FY) 2016-08-26 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥2,990,000 (Direct Cost: ¥2,300,000、Indirect Cost: ¥690,000)
Fiscal Year 2017: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
KeywordsHIV-1 / HIV-1宿主因子 / 潜伏感染 / COMMD1 / 転写制御 / ウイルス
Outline of Final Research Achievements

The effect of HIV-1 host factors has identified in primary infection. However, the effect in latent infection establishment is unknown. COMMD1 inducible cell line suppressed HIV-1 replication and decreased integrated HIV-1 genome. HIV-1 latently infection establishment and reactivation effect were similar between COMMD1 high and low expressed cells. Moreover, -1kbp COMMD1 promoter construct has highest activity in both myeloid and lymphoid cells. Therefore, this study indicates that COMMD1 doesn’t have effect for HIV-1 latent infection establishment and transcriptional regulation in myeloid cells was regulated in a further upstream.

Report

(3 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Annual Research Report
  • Research Products

    (5 results)

All 2017 2016 Other

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 1 results) Presentation (1 results) Remarks (1 results)

  • [Journal Article] Restoring PU.1 induces apoptosis and modulates viral transactivation via interferon-stimulated genes in primary effusion lymphoma2017

    • Author(s)
      Goto H、Kariya R、Kudo E、Okuno Y、Ueda K、Katano H、Okada S
    • Journal Title

      Oncogene

      Volume: 36 Issue: 37 Pages: 5252-5262

    • DOI

      10.1038/onc.2017.138

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed
  • [Journal Article] nhibition of autophagy by chloroquine induces apoptosis in primary effusion lymphoma in vitro and in vivo through induction of endoplasmic reticulum stress.2016

    • Author(s)
      Masud Alam M, Kariya R, Kawaguchi A, Matsuda K, Kudo E, Okada S.
    • Journal Title

      Apoptosis.

      Volume: 10 Issue: 10 Pages: 1191-1201

    • DOI

      10.1007/s10495-016-1277-7

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Inhibition of carbonic anhydrase potentiates bevacizumab treatment in cholangiocarcinoma.2016

    • Author(s)
      Vaeteewoottacharn K, Kariya R, Dana P, Fujikawa S, Matsuda K, Ohkuma K, Kudo E, Kraiklang R, Wongkham C, Wongkham S, Okada S.
    • Journal Title

      Tumour Biol.

      Volume: 7 Issue: 7 Pages: 9023-9035

    • DOI

      10.1007/s13277-016-4785-8

    • Related Report
      2016 Annual Research Report
    • Peer Reviewed
  • [Presentation] Sp1によるHIV-1潜伏感染の維持因子COMMD1の転写制御2016

    • Author(s)
      Eriko Kudo, Manabu Taura, Seiji Okada
    • Organizer
      第64回日本ウイルス学会学術集会
    • Place of Presentation
      札幌コンベンションセンター
    • Year and Date
      2016-10-23
    • Related Report
      2016 Annual Research Report
  • [Remarks] 岡田プロジェクト研究室ホームページ

    • URL

      http://www.caids.kumamoto-u.ac.jp/data/okada/default.html

    • Related Report
      2017 Annual Research Report 2016 Annual Research Report

URL: 

Published: 2016-09-02   Modified: 2019-03-29  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi