Regulatory RNAs and the design of cancer therapy using RNA biotechnology
Project/Area Number |
14035253
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Research Category |
Grant-in-Aid for Scientific Research on Priority Areas
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Allocation Type | Single-year Grants |
Review Section |
Biological Sciences
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Research Institution | Research Institute for Clinical Oncology, Saitama Cancer Center |
Principal Investigator |
KOZU Tomoko Research Institute for Clinical Oncology, Saitama Cancer Center, Research Institute for Clinical Oncology, Chiefinvestigator (60161874)
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Co-Investigator(Kenkyū-buntansha) |
ISHIKAWA Fuyuki Kyoto University, Graduate School of Biostudies, Department of Gene Mechanisms, Professor (30184493)
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Project Period (FY) |
2002 – 2006
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Project Status |
Completed (Fiscal Year 2006)
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Budget Amount *help |
¥67,500,000 (Direct Cost: ¥67,500,000)
Fiscal Year 2006: ¥12,400,000 (Direct Cost: ¥12,400,000)
Fiscal Year 2005: ¥12,400,000 (Direct Cost: ¥12,400,000)
Fiscal Year 2004: ¥14,200,000 (Direct Cost: ¥14,200,000)
Fiscal Year 2003: ¥14,200,000 (Direct Cost: ¥14,200,000)
Fiscal Year 2002: ¥14,300,000 (Direct Cost: ¥14,300,000)
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Keywords | nucleic acids / cancer / regulation of gene expression / RNA interference / biotechnology / telomerase / telomere / RNA aptamer / 発生・分化 / 発現抑制 |
Research Abstract |
It has recently been revealed that non-coding RNAs (regulatory RNAs) play important roles in the regulation of gene expression. The aims of this study were to manifest the role of microRNAs in hematopoietic differentiation and leukemogenesis, to clarify the regulation of telomerase activity, and to develop new methods for cancer diagnosis and therapy using RNA biotechnology on the basis of the physiological functions of regulatory RNAs. The following results were obtained: i) Knockdown of the leukemia fusion gene by siRNAs resulted in down-regulation of self-renewal activity and induction of differentiation, suggesting that these siRNAs can be used as therapeutics for leukemia; ii) MicroRNA expressions changed dynamically during differentiation to monocyte/macrophage in HL-60 cells; iii) RNA aptamers against the KRAS oncoprotein and other cancer-related proteins were obtained, which will become seeds for new methods of cancer diagnosis and therapy; iv) Telomerase is a specialized reverse transcriptase that synthesizes telomeric DNA using an intrinsic RNA template. Although the genes encoding the catalytic subunit and the template RNA have been identified, little is known about how telomerase is recruited to telomeres in vivo. In this study, we tried to biochemically identify such factors in human and fission yeast. We found that human telomerase is very resistant to extraction. However, we isolated fission yeast proteins Poz1 and Ccq1 that negatively and positively regulate telomerase.
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Report
(6 results)
Research Products
(134 results)
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[Journal Article] Characterization of a novel oncogenic K-ras mutation in colon cancer.2007
Author(s)
Akagi, K., Uchibori, R., Yamaguchi, K., Kurosawa, K., Tanaka, Y., Kozu, T.
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Journal Title
Biochem Biophys Res Commun 352
Pages: 728-732
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Journal Article] Cell-cycle-dependent Xenopus TRF1 recruitment to telomere chromatin regulated by Polo-like kinase.2006
Author(s)
Nishiyama, A., Muraki, K., Saito, M., Ohsumi, K., Kishimoto, T. Ishikawa, F.
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Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Variant forms of upstream stimulatory factors (USFs)control the promoter activity of hTERT, the human gene encoding the catalytic subunit of telomerase.2002
Author(s)
Yago, M., Ohki, R., Hatakeyama, S., Fuiita, T., Ishikawa, F.
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Journal Title
FEBS Lett 520
Pages: 40-46
Description
「研究成果報告書概要(和文)」より
Related Report
Peer Reviewed
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[Publications] Kanoh, J., Francesconi, S., Collura, A., Schramke, V., Ishikawa, F., Baldacci, G., Geli, V.: "The Fission Yeast spSet1p is a Histone H3-K4 Methyltransferase that Functions in Telomere Maintenance and DNA Repair in an ATM Kinase Rad3-dependent Pathway."J.Mol.Biol.. 326. 1081-1094 (2003)
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[Publications] Sakai, H., T.Urano, K.Ookata, M.-H.Kim, Y.Hirai, M.Saito, Y.Nojima, F.Ishikawa: "MBD3 and HDAC1, two components of the NuRD complex, are localized at Aurora-A-positive centrosomes in M phase"J. Biol. Chem.. 277. 48714-48723 (2003)
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