Details of the Researcher

PHOTO

Narufumi Kitamura
Section
Graduate School of Medicine
Job title
Associate Professor
Degree
  • Ph.D in Engineering (Kyoto University)

e-Rad No.
50624912

Research History 6

  • 2021/06 - Present
    Graduate School of Medicine, Tohoku University Department of Medical Physics Associate Professor

  • 2019/02 - 2021/05
    Graduate School of Medicine, Tohoku University Department of Medical Physics Lecturer

  • 2017/04 - 2019/01
    Graduate School of Medicine, Tohoku University Department of Medical Physics Assistant Professor

  • 2013/10 - 2017/03
    Graduate School of Medicine, Tohoku University Department of Surgical Oncology Assistant Professor

  • 2011/10 - 2013/10
    Institute for Frontier Medical Sciences, Kyoto University Department of Reparative Materials Postdoctoral fellow

  • 2006/04 - 2007/09
    KASYU CO., LTD.

Show all Show first 5

Education 4

  • Kyoto University Graduate School of Engineering Department of Polymer Chemistry

    2008/10 - 2011/09

  • Kyoto University Graduate School of Engineering Department of Chemical Engineering

    2007/10 - 2008/09

  • Kyoto University Graduate School of Engineering Department of Chemical Engineering

    2005/04 - 2006/03

  • Kyoto University Faculty of Engineering Undergraduate School of Industrial Chemistry

    2000/04 - 2005/03

Professional Memberships 4

  • Society of Nano Science and Technology

  • THE JAPANESE CANCER ASSOCIATION

  • THE SOCIETY OF POLYMER SCIENCE, JAPAN

  • THE CHEMICAL SOCIETY OF JAPAN

Research Interests 5

  • cancer

  • radiotherapy

  • nanomaterial

  • biochemistry

  • biomaterial

Research Areas 5

  • Energy / Quantum beam science / Angiography, Radiotherapy

  • Life sciences / Radiology / Angiography, Radiotherapy

  • Other / Other / pathological diagnosis Laboratory medicine

  • Nanotechnology/Materials / Polymer chemistry / nanomaterial

  • Nanotechnology/Materials / Biochemistry / Imaging Agent, Sensitizer

Papers 32

  1. Intracellular oxygen monitoring and oxygen demand assessment using Ir(ppy)3-encapsulated polymeric micelles. International-journal Peer-reviewed

    Narufumi Kitamura, Keiji Kajiwara, Shoichi Yamamoto, Mayumi Takano-Kasuya, Kunimasa Hiyama, Hiroshi Kita, Kohsuke Gonda

    Bioorganic & medicinal chemistry 137 118632-118632 2026/03/14

    DOI: 10.1016/j.bmc.2026.118632  

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    Intracellular oxygen concentration is a pivotal indicator of cellular metabolic and functional states that may be influenced by pathologic conditions, including hypoxia in solid tumors and hyperglycemia. Currently, methods for quantifying cellular oxygen levels-particularly within immune cells implicated in hypoxic dysfunction-are underdeveloped. Here, we introduce a novel biocompatible intracellular oxygen sensor developed by encapsulating the poorly water-soluble phosphorescent dye tris(2-phenylpyridinato)iridium(III) (Ir(ppy)₃) within micelles formed from 2-methacryloyloxyethyl phosphorylcholine (MPC) polymers. This micelle system enables efficient delivery and stable retention of the phosphorescent dye within the cytoplasm. Building on prior confocal microscopy studies characterizing the properties of MPC polymers, our findings reveal that cellular uptake of these polymers occurs via a cell-penetrating translocation mechanism, effectively bypassing significant endosomal sequestration and thus facilitating cytoplasmic oxygen sensing. Micelles prepared with a 30-μM Ir(ppy)₃ stock solution exhibited optimal phosphorescence and clear oxygen sensitivity. Using this sensor, we observed distinct oxygen consumption kinetics between KPL-4 and MDA-MB231 breast cancer cells. Moreover, analysis of the response of NK92-CD16 cells, an NK cell-derived immune cell line, to varying glucose levels revealed that high glucose conditions (300-400 mg/dL) significantly suppress the hypoxia-induced increase in phosphorescence, indicating reduced metabolic oxygen demand. Overall, this MPC micelle-encapsulated Ir(ppy)₃ platform serves as a robust tool for evaluating cellular metabolic states and in vitro responses to microenvironmental cues, such as hypoxia and hyperglycemia.

  2. Microregional HER2/HER3 density on cancer cells based on multi-point binding detection using nanoparticle-modified cantilever AFM Peer-reviewed

    Narufumi Kitamura, Daisuke Yamamoto, Mayumi Takano-Kasuya, Hiroshi Tada, Naoya Saito, Naoko Furusawa, Yasushi Nakano, Takanori Ishida, Kohsuke Gonda

    Colloids and Surfaces B: Biointerfaces 256 115043-115043 2025/12

    Publisher: Elsevier BV

    DOI: 10.1016/j.colsurfb.2025.115043  

    ISSN: 0927-7765

  3. Mitochondrial dynamics as a novel treatment strategy for triple-negative breast cancer. International-journal Peer-reviewed

    Yuechen Wang, Narumi Harada-Shoji, Narufumi Kitamura, Yuto Yamazaki, Akiko Ebata, Masakazu Amari, Mika Watanabe, Minoru Miyashita, Hiroshi Tada, Takaaki Abe, Takashi Suzuki, Kohsuke Gonda, Takanori Ishida

    Cancer medicine 13 (2) e6987 2024/01

    DOI: 10.1002/cam4.6987  

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    INTRODUCTION: Triple-negative breast cancer (TNBC), recognized as the most heterogeneous type of breast cancer (BC), exhibits a worse prognosis than other subtypes. Mitochondria dynamics play a vital role as mediators in tumorigenesis by adjusting to the cell microenvironments. However, the relationship between mitochondrial dynamics and metabophenotype exhibits discrepancies and divergence across various research and BC models. Therefore, this study aims to explore the role of mitochondrial dynamics in TNBC drug resistance and tumorigenesis. METHODS: The Wst-8 test was conducted to assess doxorubicin sensitivity in HCC38, MDA-MB-231 (TNBC), and MCF-7 (luminal). Confocal microscopy and FACS were used to quantify the mitochondrial membrane potential (ΔφM), mitophagy, and reactive oxygen species (ROS) production. Agilent Seahorse XF Analyzer was utilized to measure metabolic characteristics. Dynamin-related protein-1 (DRP1), Parkin, and p62 immunohistochemistry staining were performed using samples from 107 primary patients with BC before and after neoadjuvant chemotherapy (NAC). RESULTS: MDA-MB-231, a TNBC cell line with reduced sensitivity to doxorubicin, reduced ΔφM, and enhanced mitophagy to maintain ROS production through oxidative phosphorylation (OXPHOS)-based metabolism. HCC38, a doxorubicin-sensitive cell line, exhibited no alterations in ΔφM or mitophagy. However, it demonstrated an increase in ROS production and glycolysis. Clinicopathological studies revealed that pretreatment (before NAC) expression of DRP1 was significant in TNBC, as was pretreatment expression of Parkin in the hormone receptor-negative group. Furthermore, low p62 levels seem to be a risk factor for recurrence-free survival. CONCLUSION: Our findings indicated that the interplay between mitophagy, linked to a worse clinical prognosis, and OXPHOS metabolism promoted chemotherapy resistance in TNBC. Mitochondrial fission is prevalent in TNBC. These findings suggest that targeting the unique mitochondrial metabolism and dynamics in TNBC may offer a novel therapeutic strategy for patients with TNBC.

  4. Clinical Significance of ABCG2/BCRP Quantified by Fluorescent Nanoparticles in Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy Peer-reviewed

    Hiroshi Tada, Kohsuke Gonda, Narufumi Kitamura, Takanori Ishida

    Cancers 15 (8) 2365-2365 2023/04/18

    Publisher: MDPI AG

    DOI: 10.3390/cancers15082365  

    eISSN: 2072-6694

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    Breast cancer resistance protein (BCRP), also known as ATP-binding cassette transporter G2 (ABCG2), is associated with chemotherapy resistance. BCRP is also implicated in breast cancer stem cells, and is reported as a poor prognostic factor. However, the relationship of BCRP levels in breast cancer tissues with chemotherapy resistance and prognosis has not been clarified. We aimed to evaluate the correlation between BCRP expression and prognosis in breast cancer using immunohistochemistry with fluorescent phosphor-integrated dots (IHC-PIDs). A total of 37 breast cancer patients with residual cancer in the primary tumor and axillary lymph nodes were evaluated. BCRP levels in breast cancer tissue and metastatic lymph nodes were quantitatively detected after neoadjuvant chemotherapy (NAC). Among these 37 patients, 24 had corresponding core needle biopsies obtained before NAC. Biomarker assay with IHC-PIDs showed high accuracy for the quantitative assessment of BCRP with low expression. High BCRP expression in the primary tumor and metastatic lymph nodes after preoperative chemotherapy was associated with worse overall survival. In conclusion, high BCRP levels may be associated with poor prognosis in patients with breast cancer, having residual tumors within the primary tumor and lymph nodes after preoperative chemotherapy. These findings provide a basis for further appropriate adjuvant therapy in these patients.

  5. Development of gold-coated magnetic nanoparticles as a theranostic agent for magnetic hyperthermia and CT imaging applications Peer-reviewed

    Loi Tonthat, Mone Kimura, Tomoyuki Ogawa, Narufumi Kitamura, Yoshio Kobayashi, Kohsuke Gonda, Shin Yabukami

    AIP Advances 13 (2) 025239-025239 2023/02/01

    Publisher: AIP Publishing

    DOI: 10.1063/9.0000592  

    eISSN: 2158-3226

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    In this study, we aim to develop gold-coated Fe3O4 nanoparticles (Fe3O4@Au NPs) as theranostic agents for magnetic hyperthermia and CT imaging applications. The Fe3O4 NPs were synthesized via thermal decomposition method, and the gold was then deposited onto the surface of Fe3O4 NPs by reducing gold acetate at 190 °C. The average sizes of Fe3O4 and Fe3O4@Au NPs were 5.2 nm and 6.1 nm, respectively, which are effectively removed by the kidneys. The magnetization of Fe3O4@Au NPs (9.7 emu/g-Fe3O4) at 300 K was much smaller than that of Fe3O4 NPs (52.4 emu/g-Fe3O4). The heating efficiency of Fe3O4@Au NPs in water was sufficient to treat the tumor at 43–45 °C, and their high CT value of 851 HU was obtained. The synthesized ultrasmall Fe3O4@Au NPs showed great promise as a potential theranostic agent for magnetic hyperthermia and CT imaging applications.

  6. X-ray irradiation negatively affects immune responses in the lymphatic network Peer-reviewed

    Sawa Kanabuchi, Narufumi Kitamura, Mayumi Takano-Kasuya, Tomoya Inose, Chihiro Nishidate, Mizuki Yamanashi, Makoto Kudo, Tatsuki Ito, Naho Ito, Hiroshi Okamoto, Yusuke Taniyama, Yoshio Kobayashi, Takashi Kamei, Kohsuke Gonda

    Microvascular Research 104511-104511 2023/02

    Publisher: Elsevier BV

    DOI: 10.1016/j.mvr.2023.104511  

    ISSN: 0026-2862

  7. Development of X-ray contrast agents using single nanometer-sized gold nanoparticles and lactoferrin complex and their application in vascular imaging Peer-reviewed

    Tomoya Inose, Narufumi Kitamura, Mayumi Takano-Kasuya, Masayuki Tokunaga, Norikazu Une, Chihiro Kato, Mayu Tayama, Yukina Kobayashi, Noriko Yamauchi, Daisuke Nagao, Takuji Aimiya, Naoko Furusawa, Yasushi Nakano, Yoshio Kobayashi, Kohsuke Gonda

    Colloids and Surfaces B: Biointerfaces 203 111732-111732 2021/07

    Publisher: Elsevier BV

    DOI: 10.1016/j.colsurfb.2021.111732  

    ISSN: 0927-7765

  8. The anti-angiogenic agent lenvatinib induces tumor vessel normalization and enhances radiosensitivity in hepatocellular tumors International-journal Peer-reviewed

    Norikazu Une, Mayumi Takano-Kasuya, Narufumi Kitamura, Mineto Ohta, Tomoya Inose, Chihiro Kato, Ryuichi Nishimura, Hiroshi Tada, Shigehito Miyagi, Takanori Ishida, Michiaki Unno, Takashi Kamei, Kohsuke Gonda

    Medical Oncology 38 (6) 60-60 2021/06

    Publisher: Springer Science and Business Media LLC

    DOI: 10.1007/s12032-021-01503-z  

    ISSN: 1357-0560

    eISSN: 1559-131X

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    The evaluation of angiogenesis inhibitors requires the analysis of the precise structure and function of tumor vessels. The anti-angiogenic agents lenvatinib and sorafenib are multi-target tyrosine kinase inhibitors that have been approved for the treatment of hepatocellular carcinoma (HCC). However, the different effects on tumor vasculature between lenvatinib and sorafenib are not well understood. In this study, we analyzed the effects of both drugs on vascular structure and function, including vascular normalization, and investigated whether the normalization had a positive effect on a combination therapy with the drugs and radiation using micro X-ray computed tomography with gold nanoparticles as a contrast agent, as well as immunohistochemical analysis and interstitial fluid pressure (IFP) measurement. In mice subcutaneously transplanted with mouse HCC cells, treatment with lenvatinib or sorafenib for 14 days inhibited tumor growth and reduced the tumor vessel volume density. However, analysis of integrated data on vessel density, rates of pericyte-covering and perfused vessels, tumor hypoxia, and IFP measured 4 days after drug treatment showed that treatment with 3 mg/kg of lenvatinib significantly reduced the microvessel density and normalized tumor vessels compared to treatment with 50 mg/kg of sorafenib. These results showed that lenvatinib induced vascular normalization and improved the intratumoral microenvironment in HCC tumors earlier and more effectively than sorafenib. Moreover, such changes increased the radiosensitivity of tumors and enhanced the effect of lenvatinib and radiation combination therapy, suggesting that this combination therapy is a powerful potential application against HCC.

  9. Heterogeneous Drug Efficacy of an Antibody-Drug Conjugate Visualized Using Simultaneous Imaging of Its Delivery and Intracellular Damage in Living Tumor Tissues Peer-reviewed

    Kohsuke Gonda, Hiroshi Negishi, Mayumi Takano-Kasuya, Narufumi Kitamura, Naoko Furusawa, Yasushi Nakano, Yoh Hamada, Masayuki Tokunaga, Hideo Higuchi, Hiroshi Tada, Takanori Ishida

    TRANSLATIONAL ONCOLOGY 13 (6) 100764-100764 2020/06

    DOI: 10.1016/j.tranon.2020.100764  

    ISSN: 1936-5233

  10. A millisecond structured illumination microscope for super-resolution live cell imaging Peer-reviewed

    Tomu Suzuki, Shinji Kajimoto, Narufumi Kitamura, Mayumi Takano-Kasuya, Naoko Furusawa, Yasushi Nakano, Hiroshi Fukumura, Kohsuke Gonda, Takakazu Nakabayashi

    Applied Physics Express 13 (4) 045002 (4 page) 2020/03

    DOI: 10.35848/1882-0786/ab7cef  

  11. Automated Quantification of Extranuclear ERα using Phosphor-integrated Dots for Predicting Endocrine Therapy Resistance in HR+/HER2- Breast Cancer. International-journal Peer-reviewed

    Zhaorong Guo, Hiroshi Tada, Narufumi Kitamura, Yoh Hamada, Minoru Miyashita, Narumi Harada-Shoji, Akiko Sato, Yohei Hamanaka, Kouki Tsuboi, Nobuhisa Harada, Mayumi Takano-Kasuya, Hisatake Okada, Yasushi Nakano, Noriaki Ohuchi, Shin-Ichi Hayashi, Takanori Ishida, Kohsuke Gonda

    Cancers 11 (4) 2019/04/12

    DOI: 10.3390/cancers11040526  

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    In addition to genomic signaling, Estrogen receptor alpha (ERα) is associated with cell proliferation and survival through extranuclear signaling contributing to endocrine therapy (ET) resistance. However, the relationship between extranuclear ERα and ET resistance has not been extensively studied. We sought to measure extranuclear ERα expression by immunohistochemistry using phosphor-integrated dots (IHC-PIDs) and to assess its predictive value for ET resistance. After quantitative detection of ERα by IHC-PIDs in vitro, we developed "the nearest-neighbor method" to calculate the extranuclear ERα. Furthermore, tissue sections from 65 patients with HR+/HER2- BC were examined by IHC-PIDs, and the total ERα, nuclear ERα, extranuclear ERα PIDs score, and ratio of extranuclear-to-nuclear ERα (ENR) were measured using the novel method. We demonstrate that quantification of ERα using IHC-PIDs exhibited strong correlations to real-time qRT-PCR (r2 = 0.94) and flow cytometry (r2 = 0.98). High ERα ENR was significantly associated with poor overall survival (p = 0.048) and disease-free survival (DFS) (p = 0.007). Multivariate analysis revealed that the ERα ENR was an independent prognostic factor for DFS [hazard ratio, 3.8; 95% CI, 1.4-11.8; p = 0.006]. Our automated measurement has high accuracy to localize and assess extranuclear ERα. A high ERα ENR in HR+/HER2- BC indicates decreased likelihood of benefiting from ET.

  12. Quantitative analyses of amount and localization of radiosensitizer gold nanoparticles interacting with cancer cells to optimize radiation therapy Peer-reviewed

    Keiichiro Hatoyama, Narufumi Kitamura, Mayumi Takano-Kasuya, Masayuki Tokunaga, Takahiro Oikawa, Mineto Ohta, Yoh Hamada, Hiroshi Tada, Yoshio Kobayashi, Takashi Kamei, Kohsuke Gonda

    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 508 (4) 1093-1100 2019/01

    DOI: 10.1016/j.bbrc.2018.12.016  

    ISSN: 0006-291X

    eISSN: 1090-2104

  13. Quantitative diagnosis of HER2 protein expressing breast cancer by single-particle quantum dot imaging Peer-reviewed

    Minoru Miyashita, Kohsuke Gonda, Hiroshi Tada, Mika Watanabe, Narufumi Kitamura, Takashi Kamei, Hironobu Sasano, Takanori Ishida, Noriaki Ohuchi

    CANCER MEDICINE 5 (10) 2813-2824 2016/10

    DOI: 10.1002/cam4.898  

    ISSN: 2045-7634

  14. X-ray computed tomography imaging of a tumor with high sensitivity using gold nanoparticles conjugated to a cancer-specific antibody via polyethylene glycol chains on their surface Peer-reviewed

    Tomohiko Nakagawa, Kohsuke Gonda, Takashi Kamei, Liman Cong, Yoh Hamada, Narufumi Kitamura, Hiroshi Tada, Takanori Ishida, Takuji Aimiya, Naoko Furusawa, Yasushi Nakano, Noriaki Ohuchi

    SCIENCE AND TECHNOLOGY OF ADVANCED MATERIALS 17 (1) 387-397 2016

    DOI: 10.1080/14686996.2016.1194167  

    ISSN: 1468-6996

    eISSN: 1878-5514

  15. Interaction between cells and poly(ethylene glycol)-lipid conjugates Peer-reviewed

    Toru Itagaki, Yusuke Arima, Rei Kuwabara, Narufumi Kitamura, Hiroo Iwata

    COLLOIDS AND SURFACES B-BIOINTERFACES 135 765-773 2015/11

    DOI: 10.1016/j.colsurfb.2015.08.014  

    ISSN: 0927-7765

    eISSN: 1873-4367

  16. A DNA hybridization system for labeling of neural stem cells with SPIO nanoparticles for MRI monitoring post-transplantation Peer-reviewed

    Edgar Y. Egawa, Narufumi Kitamura, Ryusuke Nakai, Yusuke Arima, Hiroo Iwata

    BIOMATERIALS 54 158-167 2015/06

    DOI: 10.1016/j.biomaterials.2015.03.017  

    ISSN: 0142-9612

    eISSN: 1878-5905

  17. Highly Sensitive Imaging of Cancer with Functional Nanoparticles Peer-reviewed

    Kohsuke Gonda, Yoh Hamada, Narufumi Kitamura, Hiroshi Tada, Minoru Miyashita, Takashi Kamei, Takanori Ishida, Noriaki Ohuchi

    JOURNAL OF PHOTOPOLYMER SCIENCE AND TECHNOLOGY 28 (6) 731-736 2015

    DOI: 10.2494/photopolymer.28.731  

    ISSN: 0914-9244

  18. Labeling of islet cells with iron oxide nanoparticles through DNA hybridization for highly sensitive detection by MRI Peer-reviewed

    Narufumi Kitamura, Ryusuke Nakai, Haruyasu Kohda, Keiko Furuta-Okamoto, Hiroo Iwata

    BIOORGANIC & MEDICINAL CHEMISTRY 21 (22) 7175-7181 2013/11

    DOI: 10.1016/j.bmc.2013.08.063  

    ISSN: 0968-0896

    eISSN: 1464-3391

  19. Heat-initiated detection for reduced glutathione with F-19 NMR probes based on modified gold nanoparticles Peer-reviewed

    Narufumi Kitamura, Kazuo Tanaka, Yoshiki Chujo

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 23 (1) 281-286 2013/01

    DOI: 10.1016/j.bmcl.2012.10.105  

    ISSN: 0960-894X

    eISSN: 1464-3405

  20. Reduced glutathione-resisting F-19 NMR sensors for detecting HNO Peer-reviewed

    Narufumi Kitamura, Tatsuhiro Hiraoka, Kazuo Tanaka, Yoshiki Chujo

    BIOORGANIC & MEDICINAL CHEMISTRY 20 (15) 4668-4674 2012/08

    DOI: 10.1016/j.bmc.2012.06.013  

    ISSN: 0968-0896

  21. Heavy metal-free F-19 NMR probes for quantitative measurements of glutathione reductase activity using silica nanoparticles as a signal quencher Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Yoshiki Chujo

    BIOORGANIC & MEDICINAL CHEMISTRY 20 (1) 96-100 2012/01

    DOI: 10.1016/j.bmc.2011.11.026  

    ISSN: 0968-0896

  22. Bimodal Quantitative Monitoring for Enzymatic Activity with Simultaneous Signal Increases in F-19 NMR and Fluorescence Using Silica Nanoparticle-Based Molecular Probes Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Yoshiki Chujo

    BIOCONJUGATE CHEMISTRY 22 (8) 1484-1490 2011/08

    DOI: 10.1021/bc100381x  

    ISSN: 1043-1802

  23. Reductive Glutathione-Responsive Molecular Release Using Water-Soluble POSS Network Polymers Peer-reviewed

    Kazuo Tanaka, Wataru Ohashi, Narufumi Kitamura, Yoshiki Chujo

    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN 84 (6) 612-616 2011/06

    DOI: 10.1246/bcsj.20110032  

    ISSN: 0009-2673

    eISSN: 1348-0634

  24. Biodegradable Main-Chain Phosphate-Caged Fluorescein Polymers for the Evaluation of Enzymatic Activity Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Yoshiki Chujo

    MACROMOLECULES 43 (14) 6180-6184 2010/07

    DOI: 10.1021/ma1009066  

    ISSN: 0024-9297

  25. Preparation for Highly Sensitive MRI Contrast Agents Using Core/Shell Type Nanoparticles Consisting of Multiple SPIO Cores with Thin Silica Coating Peer-reviewed

    Kazuo Tanaka, Asako Narita, Narufumi Kitamura, Wataru Uchiyama, Masahito Morita, Toshiro Inubushi, Yoshiki Chujo

    LANGMUIR 26 (14) 11759-11762 2010/07

    DOI: 10.1021/la1015077  

    ISSN: 0743-7463

  26. Reversible signal regulation system of F-19 NMR by redox reactions using a metal complex as a switching module Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Yuichi Takahashi, Yoshiki Chujo

    BIOORGANIC & MEDICINAL CHEMISTRY 17 (11) 3818-3823 2009/06

    DOI: 10.1016/j.bmc.2009.04.039  

    ISSN: 0968-0896

    eISSN: 1464-3391

  27. Improving Proton Relaxivity of Dendritic MRI Contrast Agents by Rigid Silsesquioxane Core Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Kensuke Naka, Masahito Morita, Toshiro Inubushi, Moeko Chujo, Masaya Nagao, Yoshiki Chujo

    POLYMER JOURNAL 41 (4) 287-292 2009

    DOI: 10.1295/polymj.PJ2008274  

    ISSN: 0032-3896

  28. Acceleration of guanine oxidation under visible light irradiation by photon upconversion based on triplet-triplet annihilation. Peer-reviewed

    Tanaka K, Kitamura N, Inafuku K, Chujo Y

    Nucleic acids symposium series (2004) 53 (53) 183-184 2009

    Publisher: Oxford University Press

    DOI: 10.1093/nass/nrp092  

    ISSN: 1746-8272

  29. Assembly system of direct modified superparamagnetic iron oxide nanoparticles for target-specific MRI contrast agents Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Masahito Morita, Toshiro Inubushi, Yoshiki Chujo

    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS 18 (20) 5463-5465 2008/10

    DOI: 10.1016/j.bmcl.2008.09.035  

    ISSN: 0960-894X

  30. Synthesis of Multimodal19F NMR Probes Based on Cubic Silsesquioxanes Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Yoshiki Chujo

    Photomedicine and Photobiology 30 23-24 2008/07

    Publisher: The Japanese Society for Photomedicine and Photobiology

  31. Multi-modal F-19 NMR probe using perfluorinated cubic silsesquioxane-coated silica nanoparticles for monitoring enzymatic activity Peer-reviewed

    Kazuo Tanaka, Narufumi Kitamura, Kensuke Naka, Yoshiki Chujo

    CHEMICAL COMMUNICATIONS (46) 6176-6178 2008

    DOI: 10.1039/b815022b  

    ISSN: 1359-7345

  32. Properties of superparamagnetic iron oxide nanoparticles assembled on nucleic acids. Peer-reviewed

    Tanaka K, Kitamura N, Chujo Y

    Nucleic acids symposium series (2004) (52) 693-694 2008

    DOI: 10.1093/nass/nrn350  

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Misc. 25

  1. Imaging of Venous Thrombus Formation Mechanisms Using Synchrotron Radiation and X-ray Contrast NanoParticle

    Mone KIMURA, Narufumi KITAMURA, Kohsuke GONDA

    Medical Imaging Technology 44 (2) 80-85 2026/03

  2. 遷移金属錯体を基盤としたバイオイメージング

    北村成史

    光技術動向調査報告書 2025/03

  3. 血管新生阻害剤による腫瘍血管正常化の窓の多次元解析

    當山 亮太, 細沼 由季, 熊谷 圭悟, 宇根 範和, 春田 知洋, 関川 明生, 米山 明男, 兵藤 一行, 北村 成史, 権田 幸祐

    日本DDS学会学術集会プログラム予稿集 40回 609-609 2024/07

    Publisher: 日本DDS学会

  4. 乳癌基礎研究の最前線 腫瘍血管正常化の窓のナノバイオ解析と治療応用

    権田 幸祐, 當山 亮太, 多田 寛, 米山 明男, 兵藤 一行, 石田 孝宣, 北村 成史

    日本乳癌学会総会プログラム抄録集 32回 26-26 2024/07

    Publisher: (一社)日本乳癌学会

  5. バイオイメージングにおける蛍光粒子材料の応用動向

    北村成史

    光技術動向調査報告書 2024/03

  6. 静脈血栓塞栓症の発症予測診断を目指した光計測による血栓形成機序の解明

    木村森音, 佐々木洋輔, 米山明男, 兵藤一行, 春田知洋, 関川明生, 古澤直子, 檜山邦雅, 北弘志, 北村成史, 権田幸祐, 権田幸祐

    日本血栓止血学会誌 35 (2) 2024

    ISSN: 0915-7441

  7. Multi-Dimensional Imaging of Venous Thrombosis Mechanisms by X-Ray Phase Contrast CT Using Synchrotron Radiation

    木村森音, 佐々木洋輔, 米山明男, 兵藤一行, 春田知洋, 関川明生, 古澤直子, 檜山邦雅, 北弘志, 小林芳男, 北村成史, 権田幸祐, 権田幸祐

    量子ビームサイエンスフェスタ(Web) 2023 2024

  8. 蛍光ナノ材料を用いたウイルスセンシング技術

    北村成史, 権田幸祐

    オプトニューズ 18 (4) 2023/03

  9. ナノ粒子を利用した静脈血栓形成過程のマルチモーダルイメージング

    木村森音, 佐々木洋輔, 北村成史, 権田幸祐

    ナノ学会大会講演予稿集 21st (Web) 2023

  10. 静脈血栓塞栓症の発症予測技術への応用を目指した光イメージングによる血栓形成機序の解明

    木村森音, 佐々木洋輔, 米山明男, 兵藤一行, 古澤直子, 檜山邦雅, 北弘志, 北村成史, 権田幸祐

    日本血管生物医学会学術集会プログラム・抄録集 31st (CD-ROM) 2023

  11. 有機蛍光ナノ粒子を用いた生体イメージング技術

    北村成史

    光技術動向調査報告書 2022/03

  12. Nanomedicine Using Photosensitive Nanoparticles

    西館智尋, 金野智浩, 坂本武琉, 木下菜月, 鳥井猛流, 橋本佳樹, 川内敬子, 三好大輔, 今井陽介, 小林芳男, 山内紀子, 北村成史, 権田幸祐

    ナノ学会大会講演予稿集 20th 2022

  13. 蛍光ナノ粒子を用いた乳癌バイオマーカーの高感度定量法

    多田 寛, 権田 幸祐, 北村 成史, 石田 孝宣

    日本臨床細胞学会雑誌 60 (Suppl.2) 382-382 2021/10

    Publisher: (公社)日本臨床細胞学会

    ISSN: 0387-1193

    eISSN: 1882-7233

  14. 様々な手法で見る生体試料 高輝度蛍光ナノ粒子を用いた病理解析による乳癌内分泌療法の耐性予測

    権田 幸祐, 北村 成史, 石田 孝宣, 多田 寛

    バイオイメージング 30 (2) 44-44 2021/08

    Publisher: 日本バイオイメージング学会

    ISSN: 1342-2634

  15. Visualization of Biological Information and Quantitative Evaluation of Pathological Conditions Using Functional Nanoparticles

    Narufumi Kitamura, Hiroshi Tada, Mayumi Takano-Kasuya, Yoshio Kobayashi, Takanori Ishida, Takasi Kamei, Kohsuke Gonda

    化学工業 72 (4) 258-267 2021/04

    ISSN: 0451-2014

  16. 【蛍光イメージングと癌治療】蛍光イメージングによる抗体医薬の創薬支援および薬効予測診断

    権田 幸祐, 根岸 洋, 高野 真由美, 北村 成史, 古澤 直子, 中野 寧, 多田 寛, 石田 孝宣

    癌と化学療法 48 (2) 170-175 2021/02

  17. 核外ERαの定量分析に基づくHR+/HER2乳癌の内分泌療法抵抗性の予測(Prediction of endocrine therapy resistance in HR+/HER2 breast cancer based on quantitative analysis of extranuclear ERα)

    北村 成史, 多田 寛, 濱田 庸, 宮下 穣, 原田 成美, 濱中 洋平, 坪井 洸樹, 大内 憲明, 林 慎一, 石田 孝宣, 権田 幸祐

    日本癌学会総会記事 78回 J-1030 2019/09

    Publisher: (一社)日本癌学会

    ISSN: 0546-0476

  18. 血管新生阻害剤に対する薬剤耐性を回避する新たな腫瘍兵糧攻め療法の開発

    加藤智尋, 北村成史, 徳永正之, 濱田庸, 鳩山恵一朗, 高野真由美, 福原武志, 今井陽介, 権田幸祐

    日本心血管内分泌代謝学会学術総会プログラム及び抄録集 23rd 2019

  19. Quantification of protein heterodimers by using fluorescent nanoparticles for breast cancer diagnosis

    Narufumi Kitamura, Hiroshi Tada, Kohsuke Gonda

    CANCER SCIENCE 109 521-521 2018/12

    ISSN: 1349-7006

  20. 乳がん診断技術への応用を指向した蛍光ナノ粒子によるタンパク質ヘテロダイマーの定量(Quantification of protein heterodimers by using fluorescent nanoparticles for breast cancer diagnosis)

    北村 成史, 多田 寛, 権田 幸祐

    日本癌学会総会記事 77回 557-557 2018/09

    Publisher: 日本癌学会

    ISSN: 0546-0476

  21. Prognostic value of nuclear and non-nuclear estrogen receptor expression by immunohistochemistry with phosphor-integrated dots in hormone receptor-positive early breast cancer

    Zhaorong Guo, Hiroshi Tada, Narufumi Kitamura, Yoh Hamada, Shin-ichi Hayashi, Noriaki Ohuchi, Kosuke Gonda, Takanori Ishida

    CANCER RESEARCH 78 (13) 2018/07

    DOI: 10.1158/1538-7445.AM2018-5243  

    ISSN: 0008-5472

    eISSN: 1538-7445

  22. 金ナノ粒子を用いたがん転移リンパ節への光熱療法の開発

    及川 隆洋, 権田 幸祐, 高野 真由美, 猪瀬 智也, 徳永 正之, 北村 成史, 小林 芳男, 鳩山 恵一朗, 小野寺 優, 石田 裕嵩, 丸山 祥太, 佐藤 千晃, 濱田 庸, 瓶子 隆弘, 櫻井 直, 谷山 裕亮, 亀井 尚

    日本外科学会定期学術集会抄録集 118回 2119-2119 2018/04

    Publisher: (一社)日本外科学会

  23. 腫瘍血管に対するVEGF標的薬の効果を高感度4次元X線CTイメージングで解析する

    徳永正之, 北村成史, 濱田庸, 高野真由美, 今井陽介, 権田幸祐

    日本心血管内分泌代謝学会学術総会プログラム及び抄録集 21st 110 2017

  24. 新規蛍光ナノ粒子を用いた乳癌バイオマーカーの高感度定量評価

    郭 ショウ蓉, 多田 寛, 北村 成史, 濱田 庸, 権田 幸祐, 大内 憲明

    日本癌学会総会記事 75回 P-2156 2016/10

    Publisher: 日本癌学会

    ISSN: 0546-0476

  25. Development and evaluation of labeled islet cells using iron oxide nanoparticles and DNA hybridization. Peer-reviewed

    Nakai R, Kitamura N, Iwata Hi

    Joint Annual Meeting ISMRM & ESMRMB 2014 2014

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Research Projects 14

  1. 放射線治療のアブスコパル効果を促進する腫瘍血管正常化の高分解能X線計測と応用

    権田 幸祐, 北村 成史, 多田 寛

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(B)

    Institution: 東北大学

    2025/04/01 - 2028/03/31

  2. 糖尿病におけるがんリスク増加の機序解明とがん種横断的リスク診断技術の開発

    高野 真由美, 北村 成史, 権田 幸祐

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(C)

    Institution: 東北大学

    2025/04/01 - 2028/03/31

  3. Pharmacokinetic analysis of antibody drug conjugate in tumor cells utilizing synchrotron soft X-ray imaging

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Scientific Research (B)

    Institution: National Institutes for Quantum Science and Technology

    2023/04/01 - 2026/03/31

  4. 放射線治療に有用なアブスコパル効果の発現機序解明と応用

    権田 幸祐, 多田 寛, 北村 成史

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(B)

    Institution: 東北大学

    2022/04/01 - 2025/03/31

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    放射線治療のアブスコパル効果は、研究が停滞していたが、がん免疫研究の進展で再注目されてきた。その結果、放射線照射によるがん細胞傷害が、がん抗原の露出量を増やし、これにより免疫応答を介してアブスコパル効果の発現が促進されることが分かってきた。以上の研究では、腫瘍径の値や腫瘍の一部の組織切片データを用いて解析が行われた。そのためアブスコパル効果を発現する腫瘍を、分子から組織全体に渡り統合的に計測し解析する技術に欠けており、腫瘍内で不均一に起こるアブスコパル効果の実態を正しく評価することが難しかった。本研究では、蛍光計測とX線CT計測を行い、アブスコパル効果発現の鍵となる「腫瘍微小環境」や「がん免疫応答」の経時変化に注目しつつ、両計測データを統合的に解析し、その応用としてこの効果の発現を促進・最適化させる治療法開発を試みる。 以上の研究目的を実現するため、2022年度は、血管新生阻害剤を用いたアブスコパル効果の発現を誘導する放射線治療モデルの構築を試みた。この実験では、マウスの足背に1次腫瘍として癌細胞を移植し、2日後に同マウスの腰に同じ癌細胞を移植 (2次腫瘍)した。また治療条件は、コントロール群、放射線照射群 (1次腫瘍のみ)、血管新生阻害剤投与群、併用療法群の4群で行った。その結果、腫瘍径の大きさに関して治療効果データに有意差を示す実験系の確立に成功した。 2023年度は、病理解析によって治療効果の詳細な解析を行なった。その結果、2次腫瘍において、腫瘍血管のペリサイト被覆率は、血管新生阻害剤投与群と併用療法群において促進され、また腫瘍血管面積密度あたりのCD8陽性T細胞の浸潤数が、血管新生阻害剤投与群と併用療法群で優位に増えていることが分かった。この結果は、血管新生阻害剤投与によって腫瘍血管の正常化が進み、その結果、CD8陽性T細胞の浸潤数が増加したことを示唆していた。

  5. 非標準的遺伝子四重鎖への効果的薬剤送達を基盤とする新規光線力学療法の開発

    北村 成史, 石田 孝宣, 亀井 尚, 多田 寛, 金野 智浩, 権田 幸祐

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(C)

    Institution: 東北大学

    2022/04/01 - 2025/03/31

  6. プロテオーム・メタボローム解析による乳癌の新規悪性度評価と代謝標的治療効果予測

    多田 寛, 権田 幸祐, 石田 孝宣, 原田 成美, 北村 成史

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(C)

    Institution: 東北大学

    2022/04/01 - 2025/03/31

  7. リンパネットワークのメカノバイオ解析に基づくリンパ節転移機序の解明と診断技術開発

    高野 真由美, 北村 成史, 権田 幸祐

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(C)

    Institution: 東北大学

    2022/04/01 - 2025/03/31

  8. 放射線治療に有用なアブスコパル効果の発現機序解明と応用

    権田 幸祐, 多田 寛, 北村 成史

    Offer Organization: 日本学術振興会

    System: 科学研究費助成事業

    Category: 基盤研究(B)

    Institution: 東北大学

    2022/04/01 - 2025/03/31

  9. Development of new cancer therapy by tumor blood vessel-specific radiation therapy

    GONDA Kohsuke

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Challenging Research (Exploratory)

    Institution: Tohoku University

    2019/06/28 - 2022/03/31

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    In this study, we aimed to develop a method for improving the antitumor effect of an angiogenesis inhibitor (bevacizumab). In 2019, conditions for low-dose radiation therapy to be used in combination therapy with bevacizumab administration were examined. In addition, the tumor-bearing mice administered with gold nanoparticles (AuNPs) were irradiated with radiation, and radiosensitization effect of AuNPs on tumor shrinkage was investigated. In 2020, to evaluate the histological effect of combination therapy of angiogenesis inhibitor and radiation therapy, we developed techniques to investigate the "morphological change of tumor blood vessels" and "functional change of tumor blood vessels". In 2021, those evaluation technologies developed in 2020 were applied to the evaluation of the antitumor effect of mice in combination with angiogenesis inhibitors and radiation therapy.

  10. Development of early-stage cancer detection method and radiotherapy using ultra-small gold nanoparticles

    Kitamura Narufumi

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Scientific Research (C)

    Institution: Tohoku University

    2019/04/01 - 2022/03/31

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    We prepared ultra-small gold nanoparticles with a diameter of approximately 3 nm by coating with reduced glutathione. In animal experiments using mice, it was confirmed that the nanoparticles could be excreted in urine with a half-life of less than one hour in blood. The initial plan was then slightly modified to integrate multiple gold nanoparticles on a protein basis rather than iron oxide nanoparticles. As a result, biodegradable nanoparticles with 3~4 gold nanoparticles bound on protein particles of about 10~20 nm in diameter were successfully synthesized. The results of CT imaging analysis showed that synthesized nanoparticles had different blood convection times depending on the size and properties of the scaffold protein. The gold nanoparticles can be used as a contrast agent to delineate tiny blood vessels in tumors.

  11. Clinical significance of ABCG2/BCRP quantified by fluorescence nanoparticle in breast cancer patients undergoing neoadjuvant chemotherapy

    TADA Hiroshi

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Scientific Research (C)

    Institution: Tohoku University

    2017/04/01 - 2022/03/31

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    We aimed to evaluate the correlation between BCRP expression and prognosis in breast cancer tissue samples using immunohistochemistry with fluorescent phosphor-integrated dots (IHC-PIDs). A total of 37 breast cancer patients with residual cancer in the primary tumor and axillary lymph node were evaluated. BCRP levels in breast cancer tissue (PT) and metastatic lymph nodes (LN) were quantitatively detected after preoperative chemotherapy (NAC) and core needle biopsy (CNB). Biomarker assay with IHC-PIDs showed high accuracy for quantitative assessment of BCRP with low expression. High BCRP expression in Primary tumor and lymphnode after NAC was associated with worse overall survival (log-rank, p=0.0089). In conclusion, high BCRP levels are associated with poor prognosis in breast cancer patients with residual tumor in the primary tumor and lymph node after preoperative chemotherapy. These findings provide a basis for further appropriate adjuvant therapy in these patients.

  12. Detection of HER family dimers and prediction of anticancer drug efficacy based on single particle imaging

    Kitamura Narufumi

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Young Scientists (B)

    Institution: Tohoku University

    2017/04/01 - 2019/03/31

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    We found that the HER2 / HER3 heterodimer can be detected by a technology developed using FRET between fluorescent nanoparticles developed independently. Furthermore, in order to clarify whether this physical phenomenon correctly detects the dimer, the efficiency of energy transfer is studied using a sample in which the distance between fluorescent particles is controlled, and the energy transfer is generally performed only when the dimer is formed. However, some of the particles that are the donor of the fluorescence and the particles that are the acceptor do not correspond on a one-to-one basis, or some of the particles that only exist in the vicinity without forming a dimer were detected. It is necessary to continue to consider the method of evaluation excluding

  13. Three dimensional tissue regeneration through multipoint molecular weak association

    IWATA Hiroo, OKAMOTO Yukihiro, KITAMURA Narufumi, ARIMA Yusuke

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

    Institution: Kyoto University

    2011/04/01 - 2016/03/31

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    The aim of this study is manipulation of cellular function through the modification of cell surface. We used single-stranded DNA, which was conjugated both to poly(ethylene glycol) and to a terminal phospholipid (ssDNA-PEG-lipid) for cell surface modification. The cell surface of cells can be further functionalized through DNA hybridization. We examined control of 1) biological responses and 2) cell-substrate and cell-cell attachment. 1) The modification of cell surface of endothelial cells with antioxidant-loaded liposomes reduced oxidative stress during ischemia reperfusion. The modification of cell aggregates with superparamagnetic iron oxide nanoparticles allowed for MRI monitoring post-transplantation. 2) We realized cell attachment to poly(lactic acid) scaffold in a spatially controlled manner by taking advantage of variety of DNA sequence. In addition, both cell attachment and detachment can be programmed using DNA containing the cleavage site for restriction enzyme.

  14. Development of direct monitoring method for transplanted cells by MRI based on cell-labeling with SPIO

    KITAMURA Narufumi

    Offer Organization: Japan Society for the Promotion of Science

    System: Grants-in-Aid for Scientific Research

    Category: Grant-in-Aid for Young Scientists (B)

    Institution: Kyoto University

    2012/04/01 - 2014/03/31

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    A labeling method for islet cells with superparamagnetic iron oxide nanoparticles (SPIOs) based on DNA hybridization is proposed for monitoring of transplanted islets by MRI, The surfaces of SPIOs were modified by via Michael addition by reacting oligo-(deoxyadenylic acid)-bearing a terminal thiol group at the 5'-end ((dA)20-SH) with maleic acid functional groups on the SPIOs. the SPIOs were immobilized on islet cells which had been pretreated with oligo-(thymidylic acid)-poly(ethylene glycol)-phospholipid conjugates ((dT)20-PEG-DPPE) through DNA hybridization. Transmission electron microscopy observations revealed that SPIOs were initially anchored on the islet cells surfaces and subsequently transferred to endosomes or exfoliated with time. The SPIO-labeled islet cells could be clearly detected as dark spots by T2 weighted MR image, whereas non-labeled islet cells could not be detected.

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Teaching Experience 7

  1. Information and data literacy Tohoku Universit

  2. Topics and Discussions "Design and syhthesis of functional nanoparticles for bioimaging" Tohoku University

  3. Tequniques in Nuclear Medicine Tohoku University

  4. Fundamentals of Electrical Engineering Tohoku University

  5. Experiments on Radiochemistry Tohoku University

  6. Information Science Basics A Tohoku University

  7. Biochemistry Tohoku University

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