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1998 Fiscal Year Final Research Report Summary

Development of the Gene-missile therapy against human malignant gliomas using monocyte as a carrier.

Research Project

Project/Area Number 09671431
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Cerebral neurosurgery
Research InstitutionKumamoto University

Principal Investigator

TAKESHIMA Hideo  Kumamoto Univ.Sch.Med., Instructor, 医学部, 助手 (70244134)

Co-Investigator(Kenkyū-buntansha) SAITO Yoshiki  Kumamoto Univ.Sch.Med., Instructor, 医学部, 助手 (50304994)
NISHI Toru  Kumamoto Univ.Hosp.Instructor, 医学部・附属病院, 助手 (00264309)
KOCHI Masato  Kumamoto Univ.Sch.Med., Associate professor, 医学部, 助教授 (70178218)
USHIO Yukitaka  Kumamoto Univ.Sch.Med., Professor, 医学部, 教授 (20028583)
KURATSU Jun-ichi  Kagoshima Univ.Sch.Med., Professor (20145296)
Project Period (FY) 1997 – 1998
KeywordsMCP-1 / monocyte / CCR2 / Oct-1 / C / EBP / promoter / gene regulation / glioma
Research Abstract

The human monocyte chemoattractant protein-1 receptor designated hCCR2 is an essential co-receptor in cell entry by the human immunodeficiency virus as well as a receptor for monocyte chemoattractant protein-1, a member of the family of C-C chemokines that mediate monocyte chemotaxis. To elucidate the molecular mechanisms underlying the transcriptional regulation of hCCR2, we cloned and sequenced the hCCR2 gene ; it was approximately 8 kb in length and consisted of three exons divided by two introns. In the 5'-flanking region, there were the typical mammalian promoter consensus elements, a CAAT box and a TATA box, resulting in a single transcription initiation site. In addition, we found clustered tissue-specific cis-regulatory elements such as GATA consensus sequences, Oct-1 binding sequences, and CAAT/enhancer-binding protein binding sequences. Luciferase assays with various promoter deletions and gel mobility shift assays indicated that three cis-regulatory elements located within the region from -89 to +118 are required for basal activity in THP-1 cells. One element is an octamer sequence 36-bp upstream from the TATA box ; it binds mainly to Oct-1 and is capable of increasing transcriptional activity. The other two elements, which are tandem recognition sites of the CAAT/enhancer-binding protein family, are located in the 5'-untranslated region and account for the transcriptional activation as well as the tissue specificity of hCCR2.

  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] Takeshima,H.et al.: "Monocyte chemoattractant protein-1(MCP-1)derived from human malignant glioma.-Biological meanings of its expression and application for the treatment of malignant glioma." Research Trends. (in press). (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamamoto,K.,Takeshima,H.,et al.: "Cloning and functional characterization of the 5'-flanking region of the human monocyte chemoattractant protein-1 receptor(CCR2)gene." J.Biol.Chem.274・8. 4646-4654 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Yamamoto, K., Takeshima, H., Hamada, K., Nakao, M., Kino, T., Nishi, T., Kochi, M., Kuratsu, J., Yoshimura, T., Ushio, Y.: "Cloning and functional characterization of the 5'-flanking region of the human monocyte chemoattractant protein-1 receptor (CCR2) gene. Essential role of 5' untranslated region in tissue specific expression." J.Biol.Chem.274. 4646-4654 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takeshima, H., Kuratsu, J., Yamamoto, K., Nishi, T., Yamashiro, S., Ushio, Y., and Yoshimura, T.: "Monocyte chemoattractant protein-1 (MCP-1) derived from human malignant glioma. -Biological meanings of its expression and application for the treatment of malignant glioma." Research Trends. (in press). (1999)

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

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Published: 1999-12-08  

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