2011 Fiscal Year Final Research Report
Genomic instability in the absence of FANCJ and its possible contribution to tumorigenesis
Project/Area Number |
21590338
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Pathological medical chemistry
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Research Institution | Kyushu University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
TOKUNAGA Eriko 九州大学, 大学病院, 学術研究員 (50325453)
MORITA Masaru 九州がんセンター, 消化器外科, 医師 (30294937)
KAKEJI Yoshihiro 九州大学, 医学研究院, 准教授 (80284488)
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Project Period (FY) |
2009 – 2011
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Keywords | 分子腫瘍学 |
Research Abstract |
FANCJ is not only one of Fanconi anemia genes but also functions in cooperation with tumor suppressor gene products such as BRCA1 and MLH1. We found that(1) FANCJ deficient cells displayed a characteristic genomic instability phenotype. Moreover, we obtained clinical data that suggest that FANCJ affects anti-tumor effect of 5-FU in colorectal cancer patients.
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[Journal Article] Maehara Y. FANCJ expression predicts the response to 5-fluorouracil-based chemotherapy in MLH1-proficient colorectal cancer
Author(s)
Fujinaka Y, Matsuoka K, Iimori M, Tuul M, Sakasai R, Yoshinaga K, Saeki H, Morita M, Kakeji Y, Gillespie DA, Yamamoto K, Takata M, Kitao H
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Journal Title
Annals of Surgical Oncology(2012) in press
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[Journal Article] Maehara Y. ATR-Chk1 signaling pathway and homologous recombinational repair protect cells from 5-fluorouracil cytotoxicity
Author(s)
Fujinaka Y, Matsuoka K, Iimori M, Tuul M, Sakasai R, Yoshinaga K, Saeki H, Morita M, Kakeji Y, Gillespie DA, Yamamoto K, Takata M, Kitao H
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Journal Title
DNA Repair(Amst)
Volume: 11(3)
Pages: 247-58
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[Journal Article] High expression of BUBR1 is one of the factors for inducing DNA aneuploidy and progression in gastric cancer
Author(s)
Ando K, Kakeji Y, Kitao H, Iimori M, Zhao Y, Yoshida R, Oki E, Yoshinaga K, Matumoto T, Morita M, Sakaguchi Y, Maehara Y
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Journal Title
Cancer Science
Volume: 101(3)
Pages: 639-45
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