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Accumulation of Genetic Alterations and Chromosome Abnormalities in the Onset and Subsequent Progression of Myelodysplastic Syndromes

Research Project

Project/Area Number 12670999
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Hematology
Research InstitutionKyoto Prefecture University of Medicine

Principal Investigator

HORIIKE Shigeo  Kyoto Prefectural University of Medicine, Third Department of Internal Medicine, Assistant Professor, 医学部, 助手 (10209273)

Project Period (FY) 2000 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2002: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 2001: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 2000: ¥1,500,000 (Direct Cost: ¥1,500,000)
Keywordsmyelodysplastic syndrome / acute myeloid leukemia / genetic alteration / prognosis / p53 gene / AML1遺伝子 / 予後スコアリングシステム / p53遺伝子 / 悪性リンパ腫 / エクソンイントロン構造 / 急性白血病 / 染色体 / runtドメイン / MDS / RUNX1遺伝子 / 遺伝子多型 / GST / NQO1
Research Abstract

This project on the accumulation of genetic events during the onset and the progression of myelodysplastic syndrome (MDS) revealed three major points as follws:
(1) Refined mutational events in the Runt domain of the AML1 gone were identified in 5 patients (2.9%) of 176 patients with myeloid leukemia including 85 with MDS. Among these 5 patients, 4 exclusively showed a frame-shift mutation caused by several base-pairs deletion or insertion, resulting in V93del, 1150ins, I168ins and A120ins, respectively. Longitudinal analyses during their disease course revealed all mutations were detected in the first sample, which means AML1 mutations in MDS may be one of the earliest genetic alterations accumulated during the onset and subsequent disease progression.
(2) In order to investigate mutational events in DNA repair genes, we tried to optimize sequencing procedures for 1108 exons of 68 genes, and the optimization for 924 exons has already been finished. Among these 68 genes, we analyzed 97 exons of 6 DNA mismatch repair genes using DNA samples from marrow cells from 48 patients with MDS, 48 with malignant lymphoma, and 48 with AML. Among 79 exons (14753 base-pairs in coding regions) successfully analyzed, 31 mutational events were identified, which involved 7 in hMLH1, 1 in hMSH2, 3 in hMSH6, none in hPMS1, and 9 in hPMS2.
(3) We validated the usefulness of the International Prognostic Scoring System (IPSS) in our series of de novo MDS patients. We also revealed the prognostic significance of p53 configurations of those patients, and multivariate analysis uncovered its configuration was the most important prognostic factor, followed by the IPSS risk-stratification. Moreover, within the same IPSS category, patients with a p53 mutation showed significantly shorter survival time than those with wild-type configuration

Report

(4 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • 2000 Annual Research Report
  • Research Products

    (21 results)

All Other

All Publications (21 results)

  • [Publications] Horiike S, Kita-Sasai Y, Nakao M, Taniwaki M: "Configuration of the TP53 gene as an independent prognostic parameter of myelodysplastic syndrome"Leukemia Lymphoma. (in press). (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Nomura K, Sekoguchi S, Ueda K, Horiike S, Nishida K, Nakamura S, Taniwaki M.: "Differentiation of follicular from mucosa-associated lymphoid tissue lymphoma by detection of t(14;18) on single-cell preparations and paraffin-embedded sections"Genes Chromosomes Cancer. 33(2). 213-216 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Nakao M, Horiike S, Okuda T, et al.: "Novel insertion mutations of the hematopoiesis-related transcription factor, AML1/RUNX1, associated with myelodysplastic syndrome"BLOOD. 98(11). 352a (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Jamal R, Taketani T, Taki T, Bessho F, Hongo T, Hamaguchi H, Horiike S, et al.: "Coduplication of the MLL and FLT3 gene in patients with acute myeloid leukemia"Genes, Chromosomes & Cancer. 31(2). 187-190 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Kita-Sasai Y, Horiike S, Misawa S, Kaneko H, Kobayashi M, et al.: "International prognostic scoring system and TP53 mutations are independent prognostic indicators for patients with myelodysplastic syndrome"British Journal of Haematology. 115(2). 309-312 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Naoe T, Takeyama K, Yokoazawa T, Kiyoi H, Horiike S, et al.: "Analysis of genetic polymorphism in NQO1,GST-M1,GST-T1,and CYP3A4 in 469 Japanese patients with therapy-related leukemia/MDS and de novo AML"Clinical Cancer Research. 6(10). 4091-4095 (2000)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Horiike S, Kita-Sasai Y, Nakao M et al.: "Configuration of the TP53 gene as an independent Prognostic parameter of mayelodysplastic syndrome"Leukemia Lymphoma. in press. (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Nomura K, Sekoguchi S, Ueda K, Horiike S, et al.: "Differentiation of follicular from muco-associated lymphid tisue lymphoma by detection of t (14;18) on single cell preparations and paraffin-embedded sections"Genes Chromosomes & Cancer. 33(2). 213-216 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Nakao M, Horiike S, Okuda T, et al.: "Novel insertion mutations of the hematopoiesisrelated transcription factor, AML1/RUNX1, associated with myelodysplastic syndrome"BLOOD. 98(11). 352a (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Jurnal R, Taketani T, Taki T, Bessho F, Hongo T et al.: "Coduplication of the MLL and FLT3 gene in patients with acutemyeloid leukemia"Genes Chromosomes & Cancer. 31(2). 187-190 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Kita-Sasai Y, Hosiike S, Misawa S, Kanoko H, et al.: "International prognostic scoring system and TP53 mutations are independent prognostic indicators for patients with myelodysplastic syndrome"British Journal of Haematology. 115(2). 309-312 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Naie T, Takeyama K, Yokozawa T, Kiyoi H, et al.: "Analysis of genetic polymorphisms in NQO1, GST-M1, GST-T1, and CYP3A4 in 469 Japanese patients with therapy-related leukemia/myelodysplastic syndrome and de novo acute myeloid leukemia"Clinical Cancer Research. 6(10). 4091-4095 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] Horiike S, Kita-Sasai Y, Nakao M, Taniwaki M: "Configuration of the TP53 gene as an independent prognostic parameter of myelodysplastic syndrome"Leukemia Lymphoma. (in press). (2003)

    • Related Report
      2002 Annual Research Report
  • [Publications] Nomura K, Sekoguchi S, Ueda K, Horiike S, Nishida K, Nakamura S, Taniwaki M.: "Differentiation of follicular from mucosa-associated lymphoid tissue lymphoma by detection of t(14;18) on single-cell preparations and paraffin-embedded sections"Genes Chromosomes Cancer. 33(2). 213-216 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Nomura K, Sekoguchi S, Ueda K, Horiike S, Nishida K, Nakamura S, Taniwaki M.: "Differntiation of follicular from mucosa-associated lymphoid tissue lymphoma by detection of t(14;18)on single-cell preparations and paraffinembedded sections"Genes Chromosomes Cancer. 33(2). 213-216 (2002)

    • Related Report
      2001 Annual Research Report
  • [Publications] Jamal R, Taketani T, Taki T, Bessho F, Hongo T, Hamaguchi H, Horiike S, et al.: "Coduplication of the MLL and FLT3 gene in patients with acute myeloid leukemia"Genes, Chromosomes & Cancer. 31(2). 187-190 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Kita-Sasai Y, Horiike S, Misawa S, Kaneko H, Kobayashi M, et al.: "International prognostic scoring system and TP53 mutations are independent prognostic indicators for patients with myelodysplastic syndrome"British Journal of Haematology. 115(2). 309-312 (2001)

    • Related Report
      2001 Annual Research Report
  • [Publications] Nakazawa N,Nishida K,Tamura A,kobayashi M,Iwai T,Horiike S, et al.: "Interphase detection of t (4;14)(p16.3;q32.3) by in situ hybridization and FGFR3 overexpression in plasma cell malignancies"Cancer Genetics & Cytogenetics. 117(2). 89-96 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Naoe T,Takeyama K,Yokozawa T,Kiyoi H,Seto M,Uike N,Ino T, et al.: "Analysis of genetic polymorphism in NQO1, GST-M1, GST-T1 and CYP3A4 in 469 Japanese patients with therapy-related leukemia/MDS and de novo AML"Clinical Cancer Research. 6(10). 4091-4095 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Kuroda J,Kimura S,Akaogi T,Hayashi H,Yamano T,Sasai Y,Horiike S, et al.: "Myelodysplastic syndrome with clonal eosinophilia accompanied by eosinophilic pulmonary interstitial infiltration"Acta Haematologica. 104(2). 119-123 (2000)

    • Related Report
      2000 Annual Research Report
  • [Publications] Jamal R,Taketani T,Taki T,Bessho F,Hongo T,Hamaguchi H,Horiike S,et al.: "Coduplication of the MLL and FLT3 gene in patients with acute myeloid leukemia"Genes, Chromosomes & Cancer. (in press). (2001)

    • Related Report
      2000 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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