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Development of hormone-dependent salivary cancer therapy based on the comprehensive understanding of androgen receptor

Research Project

Project/Area Number 16K19090
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Human pathology
Research InstitutionFujita Health University

Principal Investigator

Sakurai Kouhei  藤田保健衛生大学, 医学部, 助教 (10608756)

Project Period (FY) 2016-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2017: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2016: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Keywords唾液腺導管癌 / 転写因子 / FOXA1 / マイクロアレイ / アンドロゲン受容体 / 転写制御 / mRNA / 唾液腺腫瘍 / 病理学 / 分子生物学
Outline of Final Research Achievements

The purpose of this study is to reveal the molecular pathogenesis of salivary duct carcinoma (SDC). SDC, an androgen receptor (AR)-positive malignancy, is a relatively rare salivary cancer characterized by extremely poor outcome. The growth of SDC is reported to be androgen dependent. Although androgen deprivation therapy (ADT) might be effective in SDC based on its effect on other AR-expressing cancers, such as prostate cancer (PCa) and apocrine carcinoma of the breast (ACB), its detailed gene expression signature in SDC is unclear. In this study we compare the gene expressions of SDC, PCa and ACB to reveal their shared and distinct features. We aim to identify novel diagnostic marker and develop therapeutic strategy for SDC.

Report

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

    (15 results)

All 2018 2017 2016

All Journal Article (3 results) (of which Peer Reviewed: 3 results,  Open Access: 1 results) Presentation (12 results)

  • [Journal Article] Unveiling the protein coding-independent function of the TET family in gastric cancer2018

    • Author(s)
      Sakurai, K., Tsukamoto, T.
    • Journal Title

      Non-coding RNA Investig

      Volume: 2 Pages: 17-17

    • DOI

      10.21037/ncri.2018.03.03

    • Related Report
      2017 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Visualization of neutrophil extracellular traps and fibrin meshwork in human fibrinopurulent inflammatory lesions. II. Ultrastructural study2016

    • Author(s)
      Onouchi T, Shiogama K, Matsui T, Mizutani Y, Sakurai K, Inada K, Tsutsumi Y
    • Journal Title

      Acta Histochemica et Cytochemica

      Volume: 49 Pages: 117-123

    • NAID

      130005262541

    • Related Report
      2016 Research-status Report
    • Peer Reviewed
  • [Journal Article] Visualization of neutrophil extracellular traps and fibrin meshwork in human fibrinopurulent inflammatory lesions. I. Light microscopic study2016

    • Author(s)
      Shiogama K, Onouchi T, Mizutani Y, Sakurai K, Inada K, Tsutsumi Y
    • Journal Title

      Acta Histochemica et Cytochemica

      Volume: 49 Pages: 109-116

    • NAID

      130005262535

    • Related Report
      2016 Research-status Report
    • Peer Reviewed
  • [Presentation] DNA二重鎖切断マーカーγ-H2AXを用いた胃発がん物質の短期同定2018

    • Author(s)
      岡部麻子、桐山諭和、鈴木周五、櫻井浩平、高橋智、塚本徹哉
    • Organizer
      第34回 日本毒性病理学会学術集会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 大腸癌先進部における低分化胞巣とDesmoplastic reactionとリンパ球浸潤の検討2017

    • Author(s)
      荒川敏、伊勢谷昌志、冨重博一、川辺則彦、永田英俊、浅野之夫、伊藤良太郎、清水謙太郎、稲田健一、櫻井浩平、堀口明彦
    • Organizer
      第26回 日本癌病態治療研究会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 炎症性細胞診標本中に好中球細胞外トラップは存在するのか?2017

    • Author(s)
      塩竈和也、櫻井浩平、稲田健一、堤寛
    • Organizer
      第58回 日本臨床細胞学会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 細胞診標本における好中球細胞外トラップの証明2017

    • Author(s)
      塩竈和也、尾之内高慶、水谷泰嘉、櫻井浩平、稲田健一、堤寛
    • Organizer
      第106回 日本病理学会総会
    • Related Report
      2017 Annual Research Report
  • [Presentation] NETsとフィブリンの微細構造解析2017

    • Author(s)
      尾之内高慶、塩竈和也、水谷泰嘉、櫻井浩平、稲田健一、堤寛
    • Organizer
      第106回 日本病理学会総会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 酵素抗原法の技術開発:パラフィン包埋切片において固定法が抗体活性におよぼす影響2017

    • Author(s)
      水谷泰嘉、塩竈和也、尾之内高慶、櫻井浩平、稲田健一、堤寛
    • Organizer
      第106回 日本病理学会総会
    • Related Report
      2017 Annual Research Report
  • [Presentation] 前立腺癌進展に関与するアンドロゲン受容体制御性non-coding RNA clusters2016

    • Author(s)
      櫻井浩平
    • Organizer
      第39回 日本分子生物学会年会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2016-11-30
    • Related Report
      2016 Research-status Report
  • [Presentation] アンドロゲン受容体とパイオニアリングファクターFOXA1が、唾液腺導管癌の診断と治療に与 える影響2016

    • Author(s)
      櫻井浩平、笠原正男、水谷泰嘉、稲田健一
    • Organizer
      第75回 日本癌学会総会
    • Place of Presentation
      パシフィコ横浜
    • Year and Date
      2016-10-06
    • Related Report
      2016 Research-status Report
  • [Presentation] Shared molecular and pathological features among salivary duct carcinoma, prostate and breast cancers expressing androgen receptor and FOXA12016

    • Author(s)
      Sakurai K, Kusafuka K, Kawai R, Urano M, Kuroda M
    • Organizer
      第27回 日本臨床口腔病理学会総会
    • Place of Presentation
      広島大学
    • Year and Date
      2016-08-10
    • Related Report
      2016 Research-status Report
  • [Presentation] AR 陽性唾液腺導管癌の進展におけるFOXA1 の分子病理学的解析2016

    • Author(s)
      櫻井浩平、和佐野浩一郎、川崎泰士、草深公秀、浦野誠
    • Organizer
      第40 回日本頭頸部癌学会
    • Place of Presentation
      埼玉ソニックシティ
    • Year and Date
      2016-06-09
    • Related Report
      2016 Research-status Report
  • [Presentation] 唾液腺導管癌のアンドロゲン遮断療法に対する抵抗性とFOXA1 の発現変動の関連について2016

    • Author(s)
      和佐野浩一郎、川崎泰士、櫻井浩平
    • Organizer
      第40 回日本頭頸部癌学会
    • Place of Presentation
      埼玉ソニックシティ
    • Year and Date
      2016-06-09
    • Related Report
      2016 Research-status Report
  • [Presentation] ホルモン制御性long non-coding RNA であるDRAIC は、前立腺癌の浸潤を抑制する2016

    • Author(s)
      櫻井浩平、塩竃和也、水谷泰嘉、尾之内高慶、山道信毅、稲田健一、堤寛
    • Organizer
      第105 回 日本病理学会総会
    • Place of Presentation
      仙台国際センター
    • Year and Date
      2016-05-12
    • Related Report
      2016 Research-status Report

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Published: 2016-04-21   Modified: 2019-03-29  

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