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Nagao Toshikage  長尾 俊景

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NAGAO TOSHIKAGE  長尾 俊景

NAGAO Toshikage  長尾 俊景

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Researcher Number 10622798
Other IDs
Affiliation (Current) 2025: 東京科学大学, 大学院医歯学総合研究科, 講師
Affiliation (based on the past Project Information) *help 2025: 東京科学大学, 大学院医歯学総合研究科, 講師
2022 – 2023: 東京医科歯科大学, 大学院医歯学総合研究科, 講師
2021: 東京医科歯科大学, 東京医科歯科大学病院, 助教
2019 – 2020: 東京医科歯科大学, 医学部附属病院, 助教
2012 – 2013: 東京医科歯科大学, 医学部附属病院, 助教
Review Section/Research Field
Principal Investigator
Basic Section 54010:Hematology and medical oncology-related / Hematology
Keywords
Principal Investigator
難治性B細胞腫瘍 / 治療プライミング効果 / 抗体-TLRリガンド複合体 / 抗体-オリゴヌクレオチド複合体 / S化CpG-ODN / 細胞内浸透抗体 / COT / 臨床的バイオマーカー / COT(TPL2) / MYD88 / Jak2-V617F / 造血器腫瘍
  • Research Projects

    (4 results)
  • Research Products

    (17 results)
  • Co-Researchers

    (2 People)
  •  The novel TLR4 ligand-antibody conjugate effectively sensitizes refractory B-cell lymphoma to target therapies.Principal Investigator

    • Principal Investigator
      長尾 俊景
    • Project Period (FY)
      2025 – 2027
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 54010:Hematology and medical oncology-related
    • Research Institution
      Institute of Science Tokyo
  •  Therapeutic potential of novel antibody-oligonucleotide conjugate for intractable B-cell lymphomasPrincipal Investigator

    • Principal Investigator
      長尾 俊景
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 54010:Hematology and medical oncology-related
    • Research Institution
      Tokyo Medical and Dental University
  •  COT, a new molecular target in refractory B-cell malignancies and its clinical applicationPrincipal Investigator

    • Principal Investigator
      NAGAO TOSHIKAGE
    • Project Period (FY)
      2019 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 54010:Hematology and medical oncology-related
    • Research Institution
      Tokyo Medical and Dental University
  •  Mechanisms involved in degradation of activated thyrosine kinase mutants induced by anti-cancer drugs and its clinical applicationPrincipal Investigator

    • Principal Investigator
      NAGAO Toshikage
    • Project Period (FY)
      2012 – 2013
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Hematology
    • Research Institution
      Tokyo Medical and Dental University

All 2021 2020 2019 2014 2013 2012

All Journal Article Presentation

  • [Journal Article] Proliferation and survival signaling from both Jak2-V617F and Lyn involving GSK3 and mTOR/p70S6K/4EBP1 in PVTL-1 cell line newly established from acute myeloid leukemia transformed from polycythemia vera.2014

    • Author(s)
      Nagao T, Kurosu T, Umezawa Y, Nogami A, Oshikawa G, Tohda S, Yamamoto M, Miura O
    • Journal Title

      PLoS One

      Volume: 9 Issue: 1 Pages: e84746-e84746

    • DOI

      10.1371/journal.pone.0084746

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-24591384, KAKENHI-PROJECT-24790966, KAKENHI-PROJECT-26461416
  • [Journal Article] PECAM-1 is involved in BCR/ABL signaling and may downregulate imatinib-induced apoptosis of Philadelphia chromosome-positiveleukemia cells2013

    • Author(s)
      Wu N, Kurosu T, Oshikawa G, Nagao T,Miura O
    • Journal Title

      Int J Oncol

      Volume: 42(2) Issue: 2 Pages: 419-28

    • DOI

      10.3892/ijo.2012.1729

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591030, KAKENHI-PROJECT-24591384, KAKENHI-PROJECT-24790966
  • [Journal Article] Inhibition of the PI3K/Akt/GSK3 Pathway Downstream of BCR/ABL, Jak2-V617F, or FLT3-ITD Downregulates DNA Damage-Induced Chk1 Activation as Well as G2/M Arrest and Prominently Enhances Induction of Apoptosis2013

    • Author(s)
      Kurosu T, Nagao T, Wu N, Oshikawa G, Miura O
    • Journal Title

      PLoS One

      Volume: 8 Issue: 11 Pages: e79478-e79478

    • DOI

      10.1371/journal.pone.0079478

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24591384, KAKENHI-PROJECT-24790966
  • [Presentation] Involvement of TPL2/p105/STAT3 axis in tumorigenesis of ABC-DLBCL2021

    • Author(s)
      吉藤康太、本村鷹多朗、野上彩子、岡田啓五、森毅彦、長尾俊景
    • Organizer
      日本血液学会学術集会
    • Data Source
      KAKENHI-PROJECT-19K08832
  • [Presentation] Tpl2 (COT kinase) regulates cell survival and proliferation in ABC-like DLBCL.2020

    • Author(s)
      Toshikage Nagao
    • Organizer
      第82回日本血液学術集会
    • Data Source
      KAKENHI-PROJECT-19K08832
  • [Presentation] Establishment and characterization of the new ABC-type DLBCL cell line TMD122019

    • Author(s)
      Toshikage Nagao
    • Organizer
      第81回日本血液学会学術集会
    • Data Source
      KAKENHI-PROJECT-19K08832
  • [Presentation] Establishment of TNET-1, a novel cell line derived from triple-negative essential thrombocythemia2019

    • Author(s)
      Toshikage Nagao
    • Organizer
      第81回日本血液学会学術集会
    • Data Source
      KAKENHI-PROJECT-19K08832
  • [Presentation] Molecular biological analysis of a novel MYD88 mutation, L265-RPP, in Waldenstrom macrogloblinemia2013

    • Author(s)
      長尾 俊景, 梅澤 佳央, 野上 彩子, 黒須 哲也, 三浦 修
    • Organizer
      第75回日本血液学会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] Molecular biological analysis of a novel MYD88 mutation, L265-RPP, in Waldenstrom macroglobulinemia2013

    • Author(s)
      Nagao T, Umezawa Y, Nogami A, Kurosu T, Miura O.
    • Organizer
      第75回日本血液学会総会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] Molecular basis for differential response of Flt3-ITD and TKD toPI3K/Akt and proteasome inhibitors2013

    • Author(s)
      野上 彩子, 押川 学, 福武 周作, 長尾 俊景, 梅澤 佳央, 黒須 哲也, 三浦 修
    • Organizer
      第75回日本血液学会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] Molecular basis for differential response of Flt3-ITD and TDK to PI3K/Akt and proteasome inhibitors.2013

    • Author(s)
      野上 彩子、押川 学、福武 周作、長尾 俊景、梅澤 佳央、黒須 哲也、三浦 修
    • Organizer
      第75回日本血液学会総会
    • Place of Presentation
      札幌
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] Flt3-ITD及びFlt3-TKD発現細胞の分子標的薬への感受性の差違とその分子基盤2012

    • Author(s)
      押川 学、長尾 俊景、野上 彩子、呉 楠、黒須 哲也、三浦 修
    • Organizer
      第74回日本血液学会学術集会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] 新規樹立Jak2-V617F発現白血病細胞株PV-T1でのLyn活性化を伴う細胞増殖シグナル伝達機構2012

    • Author(s)
      長尾 俊景、山本 正英、押川 学、野上 彩子、呉 楠、黒須 哲也、東田 修二、三浦 修
    • Organizer
      第74回日本血液学会学術集会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] 新規樹立Jak2-V617F 発現白血病細胞株PV-T1 でのLyn 活性化を伴う細胞増殖シグナル伝達機構2012

    • Author(s)
      長尾 俊景, 山本 正英, 押川 学, 野上 彩子, 呉 楠, 黒須 哲也, 東田 修二, 三浦 修
    • Organizer
      第74回日本血液学会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] BCR/ABL 発現細胞におけるChk1 とp53 を介した細胞周期チェックポイント活性化の相互調節機構2012

    • Author(s)
      黒須 哲也, 呉 楠, 野上 彩子, 押川学, 長尾 俊景, 三浦 修
    • Organizer
      第74回日本血液学会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] BCR/ABL発現細胞におけるChk1とp53を介した細胞周期チェックポイント活性化の相互調節機構2012

    • Author(s)
      黒須 哲也、呉 楠、野上 彩子、押川 学、長尾 俊景、三浦 修
    • Organizer
      第74回日本血液学会学術集会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-24790966
  • [Presentation] Flt3-ITD 及びFlt3-TKD 発現細胞の分子標的薬への感受性の差異とその分子基盤2012

    • Author(s)
      押川 学, 長尾 俊景, 野上 彩子, 呉楠, 黒須 哲也, 三浦 修
    • Organizer
      第74回日本血液学会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-24790966
  • 1.  黒須 哲也
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 2.  三浦 修
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results

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