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Investigation to determine the cause of interstitial pneumonia by the EGFR inhibitors, and the development of that suppression method

Research Project

Project/Area Number 20791210
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeSingle-year Grants
Research Field Otorhinolaryngology
Research InstitutionYokohama City University

Principal Investigator

ISHIGURO Yukari  Yokohama City University, 医学研究科, 特任助教 (00423830)

Project Period (FY) 2008 – 2009
Project Status Completed (Fiscal Year 2009)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2009: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2008: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
KeywordsEGFR阻害剤 / 間質性肺炎
Research Abstract

Acute interstitial pneumonia is one of serious side effects of epidermal growth factor receptor (EGFR) inhibitor, although that cause is still unknown. Here we report that cancer cells treated with EGFR inhibitors induce fibrosis of normal lung cell. Human tangue squamous cell carcinoma (HSC-3) was cultured with EGFR-tyrosine kinase inhibitor (AG1478) or EGFR antibody. IL-6 expression level was elevated by EGFR inhibitors in HSC-3. Those supernatants were used as the conditioned medium. Then, OUS-11, normal human lung fibroblast-like cell line, was cultured with the conditioned medium. We investigated the expression of collagen, which was the marker for fibrosis, to confirm whether fibrosis was induced or not in OUS-11. That result showed that the expression level of collagen in OUS-11 treated with conditioned medium was higher than control cells. These data suggested that acute interstitial pneumonia was induced IL-6 from cancer cells treated with EGFR inhibitors.

Report

(3 results)
  • 2009 Annual Research Report   Final Research Report ( PDF )
  • 2008 Annual Research Report
  • Research Products

    (12 results)

All 2010 2009 2008

All Journal Article (7 results) (of which Peer Reviewed: 7 results) Presentation (5 results)

  • [Journal Article] Antitumor effects of lapatinib (GW572016), a dual inhibitor of EGFR anf HER-2, in combination with cisplatin or paclitaxel on head and neck squamous cell carcinoma.2010

    • Author(s)
      Kondo N, Tsukuda M, Ishiguro Y, Kimura M, Fujita K, Sakakibara A, Takahashi H, Toth G, Matsuda H.
    • Journal Title

      Oncol Rep. 23(4)

      Pages: 957-963

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Journal Article] aPKClambda/iota promotes growth of prostate cancer cells in an autocrine manner through transcriptional activation of interleukin-6.2009

    • Author(s)
      Ishiguro H, Akimoto K, Nagashima Y, Kojima Y, Sasaki T, Ishiguro-Imagawa Y, Nakaigawa N, Ohno S, Kubota Y, Uemura H
    • Journal Title

      Proc Natl Acad Sci U S A 106(38)

      Pages: 16369-74

    • Related Report
      2009 Final Research Report
    • Peer Reviewed
  • [Journal Article] Restoration of BRAK / CXCL14 gene expression by gefitinib is associated with antitumor efficacy of the drug in head and neck squamous cell carcinoma.2009

    • Author(s)
      Ozawa S, Kato Y, Ito S, Komori R, Shiiki N, Tsukinoki K, Ozono S, Maehata Y, Taguchi T, Imagawa-Ishiguro Y, Tsukuda M, Kubota E, Hata R
    • Journal Title

      Cancer Sci. 100(11)

      Pages: 2202-9

    • Related Report
      2009 Final Research Report
    • Peer Reviewed
  • [Journal Article] Antitumor effects of lapatinib (GW572016), a dual inhibitor of EGFR and HER-2, in combination with cisplatin or paclitaxel on head and neck squamous cell carcinoma.2009

    • Author(s)
      Kondo N, Tsukuda M, Ishiguro Y, Kimura M, Fujita K, Sakakibara A, Takahashi H, Toth G, Matsuda H
    • Journal Title

      Oncol Rep. 23(4)

      Pages: 957-63

    • Related Report
      2009 Final Research Report
    • Peer Reviewed
  • [Journal Article] aPKClambd/iota promotes growth of prostate cancer cells in an autocrine manner through transcriptional activation of interleukin-6.2009

    • Author(s)
      Ishiguro H, Akimoto K, Nagashima Y, Kojima Y, Sasaki T, Ishiguro-Imagawa Y, Nakaigawa N, Ohno S, Kubota Y, Uemura H.
    • Journal Title

      Proc Natl Acad Sci USA. 106(38)

      Pages: 16369-16374

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Restoration of BRAK/CXCL14 gene expression by gefitinib is associated with antitumor efficacy of the drug in head and neck squamous cell carcinoma.2009

    • Author(s)
      Ozawa S, Kato Y, Ito S, Komori R, Shiiki N, Tsukinoki K, Ozono S, Maehata Y, Taguchi T, Imagawa-Ishiguro Y, Tsukuda M, Kubota E, Hata R.
    • Journal Title

      Cancer Sci. 100(1)

      Pages: 2202-2209

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Involvement of EGFR in the response of squamous cell carcinoma of the head and neck cell lines to gefitinib.2008

    • Author(s)
      Taguchi T, Tsukuda M, Imagawa-Ishiguro Y, Kato Y, Sano D
    • Journal Title

      Oncol Rep. 19(1)

      Pages: 65-71

    • Related Report
      2009 Final Research Report
    • Peer Reviewed
  • [Presentation] 頭頸扁平上皮癌において、GefitinibはBRAK/CXCL14の発現を介して抗腫瘍効果を示す2009

    • Author(s)
      加藤靖正, 田口享秀, 石黒由香利, 佃守
    • Organizer
      第22回日本バイオセラピィ学会学術集会総会
    • Place of Presentation
      大阪
    • Related Report
      2009 Final Research Report
  • [Presentation] ケモカインBRAK/CXCL14をマーカー分子とした頭頸部扁平上皮癌への新たな併用療法の試み2009

    • Author(s)
      小澤重幸, 加藤靖正, 伊藤慎, 小森令賀, 椎木直人, 槻木恵一, 前畑洋次郎, 田口享秀, 石黒(今川)由香利, 佃守, 畑隆一郎, 久保田英朗
    • Organizer
      第19回日本口腔粘膜学会総会・学術集会
    • Place of Presentation
      葉山町
    • Related Report
      2009 Final Research Report
  • [Presentation] Fibrosis of normal lung cells is caused by some particular factors from cancer cells treated with EGFR-TKI2008

    • Author(s)
      石黒由香利
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Year and Date
      2008-10-29
    • Related Report
      2008 Annual Research Report
  • [Presentation] Fibrosis of normal lung cells is caused by some particular factors from cancer cells treated with EGFR-TKI.2008

    • Author(s)
      石黒由香利, 石黒斉, 佃守
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Related Report
      2009 Final Research Report
  • [Presentation] The role of aPKC lambda in prostate cancer progression.2008

    • Author(s)
      石黒斉, 秋本和憲, 長嶋洋治, 小島康幸, 石黒由香利, 佐々木毅, 上村博司, 大野茂男, 窪田吉信
    • Organizer
      第67回日本癌学会学術総会
    • Place of Presentation
      名古屋
    • Related Report
      2009 Final Research Report

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Published: 2008-04-01   Modified: 2016-04-21  

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