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Hiroshi Sootome
Observed name:
H. Sootome
Institution:
Taiho Pharmaceutical (Japan)
Observed institutions:
GlaxoSmithKline (United Kingdom),
GlaxoSmithKline (Japan),
Taiho Pharmaceutical (Japan),
Taiho Oncology (United States)
OpenAlex ID:
A5029873173
MK-2206, an Allosteric Akt Inhibitor, Enhances Antitumor Efficacy by Standard Chemotherapeutic Agents or Molecular Targeted Drugs In vitro and In vivo
2010
·
Hiroshi Hirai
, Hiroshi Sootome
, et al.
·
Molecular Cancer Therapeutics
·
949
Futibatinib Is a Novel Irreversible FGFR 1–4 Inhibitor That Shows Selective Antitumor Activity against FGFR-Deregulated Tumors
2020
·
Hiroshi Sootome
, Hidenori Fujita
, et al.
·
Cancer Research
·
215
PDF
A model for decoding resistance in precision oncology: acquired resistance to FGFR inhibitors in cholangiocarcinoma
2024
·
L. Goyal
, D. DiToro
, et al.
·
Annals of Oncology
·
51
PDF
Discovery of Futibatinib: The First Covalent FGFR Kinase Inhibitor in Clinical Use
2023
·
Satoru Ito
, Sachie Otsuki
, et al.
·
ACS Medicinal Chemistry Letters
·
50
PDF
Abstract A270: TAS-120, a highly potent and selective irreversible FGFR inhibitor, is effective in tumors harboring various FGFR gene abnormalities.
2013
·
Hiroaki Ochiiwa
, Hidenori Fujita
, et al.
·
Molecular Cancer Therapeutics
·
28
TAS-119, a novel selective Aurora A and TRK inhibitor, exhibits antitumor efficacy in preclinical models with deregulated activation of the Myc, β-Catenin, and TRK pathways
2021
·
Akihiro Miura
, Hiroshi Sootome
, et al.
·
Investigational New Drugs
·
21
Aurora A Inhibitor TAS-119 Enhances Antitumor Efficacy of Taxanes In Vitro and In Vivo : Preclinical Studies as Guidance for Clinical Development and Trial Design
2020
·
Hiroshi Sootome
, Akihiro Miura
, et al.
·
Molecular Cancer Therapeutics
·
20
Validation of universal conditions for duplex quantitative reverse transcription polymerase chain reaction assays
2006
·
Tsuyoshi Ishii
, Hiroshi Sootome
, et al.
·
Analytical Biochemistry
·
16
Abstract A271: TAS-120, an irreversible FGFR inhibitor, was effective in tumors harboring FGFR mutations, refractory or resistant to ATP competitive inhibitors .
2013
·
Hiroshi Sootome
, Yayoi Fujioka
, et al.
·
Molecular Cancer Therapeutics
·
11
Pimitespib, an HSP90 Inhibitor, Enhances the Efficacy of PARP Inhibitors in PARP Inhibitor‐Insensitive Breast Cancer Cells
2025
·
Hiromi Muraoka
, Hiromi Kazuno
, et al.
·
Cancer Science
·
6
PDF
Practical evaluation of universal conditions for four-plex quantitative PCR
2007
·
Tsuyoshi Ishii
, Hiroshi Sootome
, et al.
·
Analytical and Bioanalytical Chemistry
·
6
Abstract 1117: Acquired resistance to ATP-competitive and irreversible FGFR inhibitors (FGFRi's): A library-based approach
2021
·
Hiroshi Sootome
, Suzuko Kato
, et al.
·
Cancer Research
·
5
A cell-based screening method for specifically detecting kinase activity
2007
·
Mikiya Suda
, Tsuyoshi Ishii
, et al.
·
Analytical and Bioanalytical Chemistry
·
5
A Selective Cellular Screening Assay for B-Raf and c-Raf Kinases
2007
·
Tsuyoshi Ishii
, Hiroshi Sootome
, et al.
·
SLAS DISCOVERY
·
3
PDF
A Robust, Target-Driven, Cell-Based Assay for Checkpoint Kinase 1 Inhibitors
2007
·
Tsuyoshi Ishii
, Hiroshi Sootome
, et al.
·
SLAS DISCOVERY
·
3
PDF
Pharmacological characteristics and clinical effectiveness of Futibatinib (Lytgobi® Tablets), a covalently-binding, irreversible FGFR1–4 inhibitor
2024
·
Katsuya Takagaki
, Ryota Okude
, et al.
·
Folia Pharmacologica Japonica
·
2
PDF
Abstract 659: Synergistic antitumor activity of futibatinib (TAS-120), a FGFR1-4 inhibitor, and PI3K pathway inhibitors
2020
·
Akihiro Miura
, Hiroshi Sootome
, et al.
·
Cancer Research
·
2
Abstract 564: Futibatinib (TAS-120) plus chemotherapy demonstrates a synergistic effect across various FGFR-deregulated cancer cell lines and xenograft models
2020
·
Hiroshi Sootome
, Akihiro Miura
, et al.
·
Cancer Research
·
2
398 TAS-119 a selective inhibitor of Aurora A kinase, potentiates taxane therapy in breast and lung cancer models
2014
·
Y. Nakatsuru
, A. Hashimoto
, et al.
·
European Journal of Cancer
·
2
Abstract A272: Intermittent treatment with TAS-120, an irreversible FGFR inhibitor, is effective in tumors harboring a FGFR gene abnormality.
2013
·
Yoko Nakatsuru
, Hiroaki Ochiiwa
, et al.
·
Molecular Cancer Therapeutics
·
2
252 TAS-2104, a Highly Potent and Selective Aurora A Inhibitor, Enhanced Antitumor Activity of Taxanes in Vivo
2012
·
K. Ishihara
, N. Masuko
, et al.
·
European Journal of Cancer
·
2
Abstract 4437: Pimitespib (TAS-116), an HSP90 inhibitor, overcomes resistance to androgen receptor pathway inhibitors in prostate cancer by simultaneously targeting several key resistance mechanisms
2025
·
Hiromi Muraoka
, Kazuhisa Minamiguchi
, et al.
·
Cancer Research
·
1
MO13-2 Covalent FGFR inhibitor futibatinib exhibits sustained antitumor effects compared with ATP-competitive inhibitors
2023
·
Hiromi Muraoka
, Hiroshi Sootome
, et al.
·
Annals of Oncology
·
1
Data from Futibatinib Is a Novel Irreversible FGFR 1–4 Inhibitor That Shows Selective Antitumor Activity against FGFR-Deregulated Tumors
2023
·
Hiroshi Sootome
, Hidenori Fujita
, et al.
·
1
Covalent FGFR inhibitor futibatinib exhibits sustained antitumor effects compared with ATP-competitive inhibitors by being less prone to ontarget resistance
2022
·
H. Sootome
, H. Muraoka
, et al.
·
European Journal of Cancer
·
1
PDF
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Works count:
57
Citation count:
1,410
H-index:
9
I10-index:
9
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