T
Taiji Ito
Researcher at University of Tokyo
Publications - 18
Citations - 1264
Taiji Ito is an academic researcher from University of Tokyo. The author has contributed to research in topics: Gene silencing & Chromatin remodeling. The author has an hindex of 16, co-authored 18 publications receiving 1199 citations.
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Journal ArticleDOI
miR-21 Gene Expression Triggered by AP-1 Is Sustained through a Double-Negative Feedback Mechanism
Shuji Fujita,Taiji Ito,Taketoshi Mizutani,Shigeru Minoguchi,Nobutake Yamamichi,Kouhei Sakurai,Hideo Iba +6 more
TL;DR: It is shown that activation protein 1 (AP-1) activates the miR-21 transcription in conjugation with the SWI/SNF complex, after PMA stimulation, through the conserved AP-1 and PU.1 binding sites in the promoter identified here.
Journal ArticleDOI
Identification of SWI·SNF Complex Subunit BAF60a as a Determinant of the Transactivation Potential of Fos/Jun Dimers
Taiji Ito,Mai Yamauchi,Mitsue Nishina,Nobutake Yamamichi,Taketoshi Mizutani,M Ui,Masao Murakami,Hideo Iba +7 more
TL;DR: It is shown that BAF60a, a subunit of the SWI·SNF chromatin remodeling complex, is a determinant of the transactivation potential of Fos/Jun dimers.
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The VEGF angiogenic switch of fibroblasts is regulated by MMP-7 from cancer cells
TL;DR: The data suggest that fibroblasts may store VEGF in a latent state in the extracellular environment for urgent use in angiogenesis, resulting in tumor-selective utilization of fibroblast-derived V EGF.
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The Brm gene suppressed at the post-transcriptional level in various human cell lines is inducible by transient HDAC inhibitor treatment, which exhibits antioncogenic potential
Nobutake Yamamichi,Mitsue Yamamichi-Nishina,Taketoshi Mizutani,Hirotaka Watanabe,Shigeru Minoguchi,Nao Kobayashi,Satoko Kimura,Taiji Ito,Naohisa Yahagi,Masao Ichinose,Masao Omata,Hideo Iba +11 more
TL;DR: It is shown here that these Brm-deficient human tumor cell lines carry a functional Brm gene, and all of the treated cells showed prolonged induction of Brm expression after the removal of HDAC inhibitors, and acquired the ability to maintain retroviral gene expression.
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A New System for Stringent, High-Titer Vesicular Stomatitis Virus G Protein-Pseudotyped Retrovirus Vector Induction by Introduction of Cre Recombinase into Stable Prepackaging Cell Lines
Tohru Arai,Kazuyuki Matsumoto,Kanako Saitoh,M Ui,Taiji Ito,Masao Murakami,Yumi Kanegae,Izumu Saito,François-Loïc Cosset,Yasuhiro Takeuchi,Hideo Iba +10 more
TL;DR: Stable prepackaging cell lines which can be converted into packaging cell lines for high-titer vesicular stomatitis virus G protein (VSV-G)-pseudotyped retrovirus vectors by the introduction of Cre recombinase-expressing adenovirus are reported on.