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

2003 Fiscal Year Final Research Report Summary

Mechanism of cancer metastasis via chemokine and its clinical application

Research Project

Project/Area Number 14571140
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General surgery
Research InstitutionKyushu University

Principal Investigator

YOSHITAKE Shinichirou  Kyushu Univ.Hospital, Research Associate, 大学病院, 助手 (80315142)

Co-Investigator(Kenkyū-buntansha) MORI Masaki  Medical Institute of Bioregulatlon Kyushu Univ., Professor, 生体防御医学研究所, 教授 (70190999)
Project Period (FY) 2002 – 2003
KeywordsFractalkine / CX3CR1 / colorectal cancer / CD3^+T lymphocyte / NK cell / RT-PCR
Research Abstract

Local and systemic immune responses are impaired in patients with colorectal cancer (CRC) and it is known that the number of tumor infiltrating lymphocytes (TILs) is considerably a few. On the otherhand, some CRC cases that much TIL were observed, are better prognosis than those of few cases. However, it is ordinary that antigenisity make lymphocyte infiltration, it is possible that Fractalkine, one of chemoattractants, without antigenisity also recruit lymphocyte for tumor lesion. We made hypothesis that Fractalkine would recruit lymphocyte in the tumor and play on important role of antitumorimmunity. We analyzed therefore the expression level of Fractaikine in CRC cell lines as well as in clinical samples. The expression level of Fractaikine was correlated with the density of TIL. The CRC cases with strong Fractalkine expression showed better prognosis than those with weak expression. These data suggest that Fractalkineitiducedbythe tumorwouldrecruitlymphocyteto tumor site and these TILs would induce better prognosis. The expression level of Fractaikine was an essential biomarker for predicting prognosis of patient with CRC. Fractalkine was considered to be one the blomarker for the detection of the patients with high risk for recurrence, who might benefit from additional therapeutic strategies such as adjuvant therapy.

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Yamaguchi, H., et al.: "Identification of HLA-A24-restricted CTL epitope from cancer-testis antigen, JNY-ESO-1,and induction of a specific anfitumor immune response."Clin Cancer Res. 10. 890-896 (2004)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamashita, K., et al.: "Clinical significance of secreted protein acidic and rich in cystein in esophageal carcinoma and its relation to carcinoma progression."Cancer. 97. 2412-2419 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamaguchi, H., et al.: "Stimulation of CD40 inhibits Fas- or chemotherapy-mediated apoptosis and increases cell motility in human gastric carcinoma cells."Int J Oncol. 23. 1697-1702 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tanaka, F et al.: "Intratumoral injection of dendritic cells after treatment of anticancer drugs induces tumor-specific antitumor effect in vivo."Int J Cancer. 101. 265-269 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shibuta, K., et al.: "Regional Expression of CXCL12/CXCR4 in Liver and Heoatocellular Carcinoma and Cell-cycle Variation during in vitro Differentiation"Jpn J Cancer Res. 93. 789-797 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 黒木 保, 井上 裕, 森 正樹: "消化器外科 レビュー:発癌機構(分担執筆)"総合医学社. 268

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamaguchi, H., et al.: "Identification of HLA-A24-restricted CTL epitope from cancer-testis antigen, NY-ESO-1, and induction of a specific antitumor immune response."Clin Cancer Res. 10. 890-896 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yamashita, K., et al.: "Clinical significance of secreted protein acidic and rich in cystein in esophageal carcinoma and its relation to carcinoma progression."Cancer. 97. 2412-2419 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yamaguchi, H., et al.: "Stimulation of CD4O inhibits Fas-or chemotherapy-mediated apoptosis and increases cell motility in human gastric carcinoma cells."Int J Oncol. 23. 1697-1702 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tanaka, F et al.: "Intratumoral injection of dendritic cells after treatment of anticancer drugs induces tumor-specific antitumor effect in vivo."Int J Cancer. 101. 265-269 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shibuta, K., et al.: "Regional Expression of CXCL12 / CXCR4 in Liver and Hepatocellular Carcinoma and Cell-cycle Variation during in vitro Differentiation"Jpn J Cancer Res. 93. 789-797 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuroki T, et al.: "SHOKAKIGEKA REVIEW : Carcinogenesis"SHOKAKIGEKA (Japanese). 268(8) (2003)

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 2005-04-19  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi