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Analyses of inhibitory effect of tumor angiogenesis, targeting the dynamism of bone marrow derived cells

Research Project

Project/Area Number 17590776
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Respiratory organ internal medicine
Research InstitutionMiyagi Cancer Center (2006)
Tohoku University (2005)

Principal Investigator

MAEMONDO Makoto  Miyagi Cancer Center, Dept.of Respirtory disease, Research Fellow, 免疫学部, 特任研究員 (40344676)

Project Period (FY) 2005 – 2006
Project Status Completed (Fiscal Year 2006)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2005: ¥1,800,000 (Direct Cost: ¥1,800,000)
KeywordsTumor angiogenesis / Bone marrow derived cell / NK4 / VEGF / pericyte / 腫瘍血管新生 / 肺癌
Research Abstract

We have studied effect of NK4 through anti-angiogenesis so far. We realized that NK4 suppressed tumor growth more effective in spite of low concentration of NK4 in tumor by intra-peritoneal injection than by intra-tumoral injection. We evaluated the recruitment of cells from bone marrow to xenograft tumor after transforming of NK4 adenovirus.
Method : Bone marrow transplantation was established below. The C57BL6 mice were exposed by lethal irradiation of 12Gy and transplanted hematopoietic stem cells from GFP mice. By this procedure, about 80% chimera mice can be obtained 2 weeks after bone marrow transplantation. Next, the chimera mice were inoculated LLC tumor infected by NK4 adenovirus (AdNK4)or Null adenovirus (AdNull). The tumor implanted in mice were measured in length and resected on day14 after inoculation and evaluated bone marrow derived cell and cells structured vessels dyed with zennon TM Tricolor Labeling Kit (Molecular probe) by laser scanning microscopy
Result : In vitro t … More here is no difference in growth of tumor cells infected with between NK4 adenovirus and Null adenovirus however, in vivo AdNK4 infected tumor were suppressed significantly in tumor growth. Though there are considerable amount of GFP positive cells infiltrated in tumor, most GFP positive cells did not merge with cells structured vessels. In resected tumor of NK4 groups, both tumor vessels and bone marrow derived cells decreased significantly. Many bone marrow derived cells were dyed with hematocyte markers (CD45 positive cells / GFP positive cells AdNK4 71.3%, AdNull 66.0% ). Interestingly, VEGF positive bone marrow derived cells decreaced considerably in tumor infected with AdNK4 compared to tumor infected with AdNull (GFP, VEGF double positive / total GFP positive cells: 36.3%, 8.2% respectively). The origin and differentiation of VEGF positive bone marrow derived cells has not unknown yet.
Conclusion : In this study, we could not find direct relation between anti-angiogenic effect and bone marrow derived cells, however, bone marrow derived cells decreased in tumor infected with NK4., These cells possibly have some effect on tumor angiogenesis in the paracrine manner. Further examination on the association among angiogenesis and bone marrow derived cells in the tumor suppressed by NK4 is needed. Less

Report

(3 results)
  • 2006 Annual Research Report   Final Research Report Summary
  • 2005 Annual Research Report
  • Research Products

    (13 results)

All 2006 2005

All Journal Article (13 results)

  • [Journal Article] Prospective phase II stuby of gefitinib for chemotherapy-naive patients with advanced non-small lung cancer with epidermal growth factor receptor gene2006

    • Author(s)
      Inoue A, Suzuki T, Fukuhara T
    • Journal Title

      J Clin Oncol 24

      Pages: 3340-3346

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Peritumoral injection of adenovirus vector sxpressing NK4 combined with gemcitabine treatment suppresses growth and metastasis of human pancreatic cancer cells implanted orthotopically in nude mice and prolongs survival2006

    • Author(s)
      Ogura Y, Mizumoto K, Nagai E
    • Journal Title

      Cancer Gene Ther 13

      Pages: 520-529

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Hepatocyte growth factor gene transfer to alveolar seppta for effective suppression of lung fibrosis2006

    • Author(s)
      Watanabe M, Ebina M, Orson F
    • Journal Title

      Mol ther 12

      Pages: 58-67

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Prospective phase II study of gefitinib for chemotherapy-naive patients with advanced non-small-cell lung cancer with epidermal growth factor receptor gene mutations2006

    • Author(s)
      Inoue A, Suzuki T, Fukuhara T
    • Journal Title

      J Clin Oncol 24

      Pages: 3340-3346

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Peritumoral injection of adenovirus vector expressing NK4 combined with gemcitabine treatment suppresses growth and metastasis of human pancreatic cancer cells implanted orthotopically in nude mice and prolongs survival2006

    • Author(s)
      Ogura Y, Mizumoto K, Nagai E
    • Journal Title

      Cancer Gene Ther 13

      Pages: 520-529

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Hepatocyte growth factor gene transfer to alveolar septa for effective suppression of lung fibrosis2006

    • Author(s)
      Watanabe M, Ebina M, Orson F
    • Journal Title

      Mol Ther 12

      Pages: 58-67

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Suppression of metastasis of human pancreatic cancer to the liver by transportal injection of recombinant adenoviral NK4 in nude mice.2005

    • Author(s)
      Murakami M, Nagai E, Mizumot K
    • Journal Title

      Int J Cancer 117

      Pages: 160-165

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Vaccination of dendritic cells loaded with Interleukin-12 secreting cancer cells augments in vivo antitumor immunity : Characteristics of syngeneic and allogeneic antigen presenting cell-cancer hybrid cells2005

    • Author(s)
      Suzuki T, Fukuhara T, Tanaka M
    • Journal Title

      Clin Cancer Res 11

      Pages: 58-66

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Suppression of peritoneal implantation of gastric cancer cells by adenovirus vector-mediated NK4 expression2005

    • Author(s)
      Fujiwara H, Kubota T, Amaike H
    • Journal Title

      Cancer Gene Ther 12

      Pages: 206-216

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Analyses of effect of NK4 on tumor angiogenesis through recruitment of bone marrow derived cells2005

    • Author(s)
      Okouchi S, Maemondo M, Toshiaki K, Tazawa R, Saijo Y, Nukiwa T.
    • Journal Title

      Nihon kokyuukigakkai zashi 43

      Pages: 275-275

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Peritumoral injection of adenovirus vector expressing NK4 combined with gemcitabine treatment suppresses growth and metastasis of human pancreatic cancer cells implanted orthotopically in nude mice and prolongs survival.2005

    • Author(s)
      Ogura, Y et al.
    • Journal Title

      Cancer Gene Ther. 9(Epub ahead of print)

    • Related Report
      2005 Annual Research Report
  • [Journal Article] T.Hepatocyte growth factor gene transfer to alveolar septa for effective suppression of lung fibrosis.2005

    • Author(s)
      Watanabe, M.et al.
    • Journal Title

      Mol Ther. 12(1)

      Pages: 58-67

    • Related Report
      2005 Annual Research Report
  • [Journal Article] Suppression of metastasis of human pancreatic cancer to the liver by transportal injection of recombinant adenoviral NK4 in nude mice.2005

    • Author(s)
      Murakami, M.et al.
    • Journal Title

      Int J Cancer. 117(1)

      Pages: 160-165

    • Related Report
      2005 Annual Research Report

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Published: 2005-04-01   Modified: 2016-04-21  

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