Development of diagnostic method and its application to treatment in GIST with particular mutations through creating monoclonal antibodies
Project/Area Number |
16H05166
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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 |
Human pathology
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Research Institution | Hyogo Medical University |
Principal Investigator |
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Project Period (FY) |
2016-04-01 – 2019-03-31
|
Project Status |
Completed (Fiscal Year 2018)
|
Budget Amount *help |
¥17,550,000 (Direct Cost: ¥13,500,000、Indirect Cost: ¥4,050,000)
Fiscal Year 2018: ¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2017: ¥5,980,000 (Direct Cost: ¥4,600,000、Indirect Cost: ¥1,380,000)
Fiscal Year 2016: ¥6,500,000 (Direct Cost: ¥5,000,000、Indirect Cost: ¥1,500,000)
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Keywords | GIST / c-kit / PDGFRA / mutation / antibody / Mutation / 病理学 / GIST / c-kit遺伝子変異 / 特異抗体 / 診断と治療 |
Outline of Final Research Achievements |
Among the gene mutations observed in GISTs, Dup-502&503 of the c-kit gene, Asp842Val of the PDGFRA gene and Del-557&558 of the c-kit gene were targeted to make specific antibodies to use for image diagnosis and therapy. High titer fraction on ELISA was obtained, but the final products of specific antibodies for them were not gained. We also investigated the clinicopathological characteristics of GISTs in NF1 patients, effective neoadjuvant imatinib therapy for giant gastric GISTs and condition of management of high-risk GIST patients in the real world.
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Academic Significance and Societal Importance of the Research Achievements |
GISTの治療はその病態解明に伴って劇的に進歩したが、分子標的治療に対する二次耐性の問題は患者のさらなる予後改善の足かせとなっている。GISTに特徴的なc-kit遺伝子やPDGFRA遺伝子の変異に対する特異的なモノクローナル抗体の作製が可能となれば、これまでの分子標的薬とは異なった機序で病気を制御できる可能性があり、画像診断にも応用できると考えたが、思いのほか抗体作製に難渋し、達成できなかった。補助金による研究終了後もさらなる工夫を行って継続したい。並行する研究では、各種GISTの病態の解明や実臨床での再発高リスクGIST症例の実態等が明らかにでき、今後のGIST診療に役立つものと考えられた。
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Report
(4 results)
Research Products
(15 results)
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[Journal Article] Adherence to the guidelines and the pathological diagnosis of high-risk gastrointestinal stromal tumors in the real world2019
Author(s)
Nishida T, Sakai Y, Takagi M, Ozaka M, Kitagawa Y, Kurokawa Y, Masuzawa T, Naito Y, Kagimura T, Hirota S, and the members of the STAR ReGISTry Study Group
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Journal Title
Gastric Cancer
Volume: 印刷中
Issue: 1
Pages: 118-125
DOI
NAID
Related Report
Peer Reviewed / Open Access
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[Journal Article] SOCS1 gene therapy has antitumor effects in imatinib-resistant gastrointestinal stromal tumor cells through FAK/PI3K signaling.2018
Author(s)
Sugase T, Takahashi T, Serada S, Fujimoto M, Ohkawara T, Hiramatsu K, Nishida T, Hirota S, Saito Y, Tanaka K, Miyazaki Y, Makino T, Kurokawa Y, Yamasaki M, Nakajima K, Hanasaki K, Kishimoto T, Mori M, Doki Y, Naka T.
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Journal Title
Gastric Cancer.
Volume: epub
Issue: 6
Pages: 968-976
DOI
NAID
Related Report
Peer Reviewed / Open Access
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[Journal Article] Genomic and transcriptomic analysis of imatinib resistance in gastrointestinal stromal tumors.2017
Author(s)
Takahashi T, Elzawahry A, Mimaki S, Furukawa E, Nakatsuka R, Nakamura H, Nishigaki T, Serada S, Naka T, Hirota S, Shibata T, Tsuchihara K, Nishida T, Kato M.
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Journal Title
Genes Chromosomes Cancer.
Volume: 56
Issue: 4
Pages: 303-313
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Detecting secondary c-KIT mutations in the peripheral blood of patients with imatinib-resistant gastrointestinal stromal tumor.2016
Author(s)
Wada N, Kurokawa Y, Takahashi T, Hamakawa T, Hirota S, Naka T, Miyazaki Y, Makino T, Yamasaki M, Nakajima K, Takiguchi S, Mori M, Doki Y.
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Journal Title
Oncology
Volume: 90
Issue: 2
Pages: 112-117
DOI
Related Report
Peer Reviewed
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[Journal Article] Clinicopathological characteristics, surgery and survival outcomes of patients with duodenal gastrointestinal stromal tumors.2016
Author(s)
Sugase T, Takahashi T, Nakajima K, Hirota S, Masuzawa T, Nishida T, Kimura Y, Miyazaki Y, Makino T, Kurokawa Y, Yamasaki M, Takiguchi S, Mori M, Doki Y.
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Journal Title
Digestion.
Volume: 94
Issue: 1
Pages: 30-36
DOI
Related Report
Peer Reviewed
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