Investigation of functional roles of mutant IDH as specific mutations in cartilage-forming tumors and its application for the development of treatment
Project/Area Number |
15H04956
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Orthopaedic surgery
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Research Institution | Kyoto University |
Principal Investigator |
Toguchida Junya 京都大学, ウイルス・再生医科学研究所, 教授 (40273502)
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Co-Investigator(Kenkyū-buntansha) |
金 永輝 京都大学, 医学研究科, 特定助教 (90620344)
岡本 健 京都大学, 医学研究科, 准教授 (30414113)
池谷 真 京都大学, iPS細胞研究所, 准教授 (20442923)
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Co-Investigator(Renkei-kenkyūsha) |
Watanabe Akira 京都大学, iPS細胞研究所, 特定拠点助教 (60506765)
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Project Period (FY) |
2015-04-01 – 2018-03-31
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Project Status |
Completed (Fiscal Year 2017)
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Budget Amount *help |
¥16,900,000 (Direct Cost: ¥13,000,000、Indirect Cost: ¥3,900,000)
Fiscal Year 2017: ¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2016: ¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2015: ¥8,060,000 (Direct Cost: ¥6,200,000、Indirect Cost: ¥1,860,000)
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Keywords | chondrosarcoma / IDH / iPSC / p16 / IDH遺伝子 / 軟骨形成性腫瘍 / iPS細胞 / 軟骨腫瘍 / 間葉系幹細胞 / 神経幹細胞 / ヒストンメチル化 / 軟骨形成腫瘍 |
Outline of Final Research Achievements |
Mutations of IDH gene are driver mutations in cartilage-forming tumors. To understand the mechanism of tumor specificity and functional role of IDH mutations in tumorigenesis of cartilage-forming tumors, we have performed experiments using human iPS cells. We established iPS cells with a drug-inducible mutant IDH gene in the AAVS1 locus and induced the expression of mutant IDH after the differentiation into mesenchymal stem cells (MSC). As a result, we have observed that mutant IDH has an inhibitor effect for the growth of MSC and as for the effects on differentiation, it inhibited osteogenesis and promoted the expression of cartel-related genes. To recapitulate the tumorigenesis in vitro, we further introduced the knock-out type mutations of p16 gene as a passenger mutation into IDH-AAVS-iPSCs and investigated the tumor forming capacity of iMSCs with mutant IDH and without p16 gene.
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Report
(4 results)
Research Products
(23 results)
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[Journal Article] Chondroblastoma of extra-craniofacial bones: Clinicopathological analyses of 103 cases.2017
Author(s)
Konishi E, Nakashima Y, Mano M, Tomita Y, Kubo T, Araki N, Morii E, Yoshikawa H, Haga H, Toguchida J, Ueda T, Osawa M, Hoshi M, Inoue T, Aono M, Yanagisawa A.
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Journal Title
Pathol Int
Volume: 67
Issue: 10
Pages: 495-502
DOI
Related Report
Peer Reviewed
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[Journal Article] BMP-SMAD-ID promotes reprogramming to pluripotency by inhibiting p16/INK4A-dependent senescence2016
Author(s)
Hayashi, Y., Hsiao, EC., Sami, S., Lancero, M., Schlieve, CR., Nguyen, T., Yano, K., Nagahashi, A., Ikeya, M., Matsumoto, Y., Nishimura, K., Fukuda, A., Hisatake, K., Tomoda, K., Asaka, I., Toguchida, J., Conklin, BR., and Yamanaka, S
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Journal Title
Proc. Natl. Acad. Sci. U S A
Volume: 113
Pages: 13057-13062
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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[Journal Article] Feasibility and efficacy of gemcitabine and docetaxel combination chemotherapy for bone and soft tissue sarcomas: multi-institutional retrospective analysis of 134 patients.2016
Author(s)
Tanaka, K., Joyama, S., Chuman, H., Hiraga, H., Morioka, H., Yoshikawa, H., Hosaka, M., Takahashi, M., Kubo, T., Hatano, H., Kaya, M., Toguchida, J., Nishida, Y., Nagano, A., Tsumura, H., and Iwamoto, Y.
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Journal Title
World J. Surg. Oncol
Volume: 14
Pages: 306-306
Related Report
Peer Reviewed
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[Journal Article] SS18-SSX, the Oncogenic Fusion Protein in Synovial Sarcoma, Is a Cellular Context-Dependent Epigenetic Modifier.2015
Author(s)
Tamaki S, Fukuta M, Sekiguchi K, Jin Y, Nagata S, Hayakawa K, Hineno S, Okamoto T, Watanabe M, Woltjen K, Ikeya M, Kato T Jr, Toguchida J.
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Journal Title
PLoS One
Volume: 10
Issue: 11
Pages: e0142991-e0142991
DOI
NAID
Related Report
Peer Reviewed / Open Access
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[Journal Article] Mutant IDH1 Dysregulates the Differentiation of Mesenchymal Stem Cells in Association with Gene-Specific Histone Modifications to Cartilage- and Bone-Related Genes.2015
Author(s)
Jin Y, Elalaf H, Watanabe M, Tamaki S, Hineno S, Matsunaga K, Woltjen K, Kobayashi Y, Nagata S, Ikeya M, Kato T Jr, Okamoto T, Matsuda S, Toguchida J.
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Journal Title
PLoS One
Volume: 10
Issue: 7
Pages: e0131998-e0131998
DOI
NAID
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Primary central chondrosarcoma of long bone, limb girdle and trunk: Analysis of 174 cases by numerical scoring on histology2015
Author(s)
Konishi E, Nakashima Y, Mano M, Tomita Y, Nagasaki I, Kubo T, Araki N, Haga H, Toguchida J, Ueda T, Sakuma T, Imahori M, Morii E, Yoshikawa H, Tsukamoto Y, Futani H, Wakasa K, Hoshi M, Hamada S, Takeshita H, Inoue T, Aono M, Kawabata K, Murata H, Katsura K, Urata Y, Ueda H, Yanagisawa A.
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Journal Title
Pathology International
Volume: 65
Issue: 9
Pages: 468-75
DOI
Related Report
Peer Reviewed / Open Access / Acknowledgement Compliant
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[Journal Article] Screening of BCOR-CCNB3 sarcoma using immunohistochemistry for CCNB3: A clinicopathological report of three pediatric cases.2015
Author(s)
Shibayama T, Okamoto T, Nakashima Y, Kato T, Sakurai T, Minamiguchi S, Kataoka TR, Shibuya S, Yoshizawa A, Toguchida J, Haga H.
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Journal Title
Pathol Int
Volume: 65
Issue: 8
Pages: 410-414
DOI
Related Report
Peer Reviewed
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[Presentation] EXPLORATION OF CANDIDATE GENES TO INDUCE CARTILAGE TUMORS WITH MUTANT IDH1 GENE USING IPSC2016
Author(s)
Kamakura, T., Jin, Y., Matsunaga, K., Watanabe, M., Tamaki, S., Okamoto, T., Yoshitomi, H., Toguchida, J
Organizer
CTOS 2016 Annual Meeting
Place of Presentation
Lisbon(Portugal)
Year and Date
2016-11-09
Related Report
Int'l Joint Research
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[Presentation] SS18-SSX, the oncogenic fusion protein in synvival sarcoma, is a cellular context-dependent epigenetic modifier2015
Author(s)
Tamaki S, Fukuta M, Sekiguchi K, Hayakawa K, Jin Y, Hineno S, Okamoto T, Watanbe M, Woltjen K, Ikeya M, Kato T, Toguchida J
Organizer
第20回CTOS
Place of Presentation
Salt Lake City(USA)
Year and Date
2015-11-05
Related Report
Int'l Joint Research
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