Identification of novel therapeutic target of melanoma with focus on gain-of-function mutation of SH3 domain of KIT
Project/Area Number |
15K15414
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Dermatology
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Research Institution | Fujita Health University (2016) Nagoya University (2015) |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
KOSHIKAWA Naohiko 神奈川県立がんセンター臨床研究所, がん生物学部, 部長 (70334282)
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Project Period (FY) |
2015-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2015: ¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
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Keywords | 悪性黒色腫 / KIT / SH3ドメイン / 色素異常症 / c-KIT |
Outline of Final Research Achievements |
The aims of this study are to identify novel theraputic targets of melanoma caused by KIT mutation, and to elucidate that a novel KIT mutation creates SH3 domain which binds to some proteins which have SH2 domain. Constitutive malignant KIT mutation expressed amelanotic melanocyte cell line, constitutive non-malignant KIT mutaion expressed amelonotic melanocyte cell line, and constitutive wild type KIT expressed amelonotic melonocyte cell line were established. The novel kit mutation was proven to create SH3 domain by proteome analysis. Some binding proteins which bound to the KIT mutation were identified. Moreover, some proteins, which overexpressed in constitutive malignant KIT mutation expressed amelonotic melonocyte cell line, were also identified.
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Report
(3 results)
Research Products
(63 results)
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[Journal Article] Pityriasis rubra pilaris type V as an auto inflammatory disease by CARD14 mutations.2017
Author(s)
Takeichi T, Sugiura K, Nomura T, Sakamoto T, Ogawa Y, Oiso N, Futei Y, Fujisaki A, Koizumi A, Aoyama Y, Nakajima K, Hatano Y, Hayashi K, Akemi Ishida-Yamamoto A, Fujiwara S, Sano S, Iwatsuki K, Kawada A, Suga Y, Shimizu H, McGrath JA, Akiyama M.
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Journal Title
JAMA Dermatol
Volume: 153
Issue: 1
Pages: 66-70
DOI
Related Report
Peer Reviewed / Int'l Joint Research / Acknowledgement Compliant
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[Journal Article] Novel and recurrent ATP2A2 mutations in Japanese patients with Darier’s disease2016
Author(s)
Noda K, Takeichi T, Okuno Y, Takama H, Miura S, Kagami S, Hino H, Nakamura Y, Fujio Y, Konohana I, Otani A, Mukai H, Sugiura K, Akiyama M.
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Journal Title
Nagoya Journal of Medical Science
Volume: 78
Issue: 4
Pages: 485-492
DOI
NAID
ISSN
2186-3326
URL
Related Report
Peer Reviewed / Int'l Joint Research
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[Journal Article] Dyschromatosis symmetrica hereditaria and Aicardi-Goutires syndrome 6 are phenotypic variants caused by ADAR1 mutations.2016
Author(s)
Kono M, Matsumoto F, Suzuki Y, Suganuma M, Saitsu H, Ito Y, Fujiwara S, Matsumoto K, Moriwaki S, Matsumoto N, Tomita Y, Sugiura K, Akiyama M.
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Journal Title
J Invest Dermatol.
Volume: 136
Issue: 4
Pages: 875-8
DOI
Related Report
Peer Reviewed / Int'l Joint Research
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[Journal Article] Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.2015
Author(s)
Kono M, Suganuma M, Takama H, Zarzoso I, Saritha M, Bodet D, Aboobacker S, Kaliaperumal K, Suzuki T, Tomita Y, Sugiura K, Akiyama M.
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Journal Title
Br J Dermatol
Volume: 173
Issue: 2
Pages: 584-6
DOI
Related Report
Peer Reviewed / Int'l Joint Research
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[Journal Article] Essential role of the cytochrome P450 CYP4F22 in the production of acylceramide, the key lipid for skin permeability barrier formation.2015
Author(s)
Ohno Y, Nakamichi S, Ohkuni A, Kamiyama N, Naoe A, Tsujimura H, Yokose U, Sugiura K, Ishikawa J, Akiyama M, Kihara A.
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Journal Title
Proc Natl Acad Sci U S A
Volume: 112
Issue: 25
Pages: 7707-12
DOI
NAID
Related Report
Peer Reviewed / Open Access
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[Journal Article] Diversity of humoral responses to the centromere proteins among HCV-related chronic liver disease, PBC and AIH patients.2015
Author(s)
Himoto T, Tanaka N, Saito A, Muro Y, Sugiura K, Tani J, Miyoshi H, Morishita A, Yoneyama H, Haba R, Masaki T.
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Journal Title
Clin Res Hepatol Gastroenterol
Volume: 39
Issue: 2
Pages: 222-229
DOI
Related Report
Peer Reviewed
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[Presentation] 先天性縮毛症・乏毛症2015
Author(s)
杉浦一充
Organizer
第20回日本臨床毛髪学会学術集会
Place of Presentation
総合あいしんセンター 高知県高知市
Year and Date
2015-12-05
Related Report
Invited
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