Moriwaki Kazumasa 森脇一将

… Alternative Names

Researcher Number	00467656
Other IDs
Affiliation (Current)	2022: 大阪医科薬科大学, 医学部, 講師
Affiliation (based on the past Project Information) *help	2021: 大阪医科薬科大学, 医学部, 助教 2017 – 2020: 大阪医科大学, 医学部, 助教 2012: 神戸大学, 大学院・医学研究科, グローバルCOE 研究員
Review Section/Research Field	Principal Investigator Pathological medical chemistry / Basic Section 50010:Tumor biology-related Except Principal Investigator General anatomy (including Histology/Embryology) / Basic Section 50020:Tumor diagnostics and therapeutics-related
Keywords	Principal Investigator O-GlcNAc修飾 / 癌 / 炎症性サイトカイン / NF-κB / p38 / 糖鎖 / 癌微小環境 Except Principal Investigator 発生学 / 形態形成学 / マウス … More

O-GlcNAc修飾による癌微小環境制御機能の解析Principal Investigator
- Principal Investigator
  
  森脇一将
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 50010:Tumor biology-related
- Research Institution
  Osaka Medical and Pharmaceutical University
Development of novel diagnosis and therapy in cancer targetting reversible system of intracellular glycosylation
- Principal Investigator
  
  竹内利寿
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 50020:Tumor diagnostics and therapeutics-related
- Research Institution
  Osaka Medical College
Role of TME O-GlcNAcylation in cancer proliferationPrincipal Investigator
- Principal Investigator
  
  Moriwaki Kazumasa
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Osaka Medical College
Pathology and molecular mechanism of embryonic edema in mice carrying endothelial gene mutations
- Principal Investigator
  
  HIRASHIMA Masanori
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  General anatomy (including Histology/Embryology)
- Research Institution
  Kobe University

All 2021 2020 2019 2018 2017

All Journal Article Presentation

[Journal Article] O-GlcNAcylation-mediated degradation of FBXL2 stabilizes FOXM1 to induce cancer progression.2020
- Author(s)
  Y Ueda, K Moriwaki, T Takeuchi, K Higuchi, and M Asahi.
- Journal Title
  
  Biochem Biophys Res Commun.
  
  Volume: 521 Pages: 632-638
- DOI
  10.1016/j.bbrc.2019.10.164
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K07762, KAKENHI-PROJECT-17K08678
[Journal Article] Augmented <i>O</i>-GlcNAcylation alleviates inflammation-mediated colon carcinogenesis via suppression of acute inflammation2018
- Author(s)
  Hirata Y, Nakagawa T, Moriwaki K, Koubayashi E, Kakimoto K, Takeuchi T, Inoue T, Higuchi K, Asahi M
- Journal Title
  
  J. Clin. Biochem. Nutr.
  
  Volume: 3 Issue: 3 Pages: 221-229
- DOI
  10.3164/jcbn.17-106
- NAID
  130006730767
- ISSN
  0912-0009, 1880-5086
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K08678, KAKENHI-PROJECT-16K09296
[Journal Article] Augmented O-GlcNAcylation of AMP-activated kinase promotes the proliferation of LoVo cells, a colon cancer cell line2017
- Author(s)
  Moriwaki K, Asahi M.
- Journal Title
  
  Mol Cancer Res.
  
  Volume: 15 Pages: 1287-1298
- DOI
  10.1158/1541-7786.mcr-16-0499
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K08678
[Presentation] O-GlcNAcylation-mediated regulation of FOXM1 expression through its ubiquitination in a human gastric adenocarcinoma cell line, NUGC-3.2021
- Author(s)
  K Moriwaki, Y Ueda, T Takeuchi, K Higuchi, and M Asahi.
- Organizer
  第94回日本薬理学会
- Data Source
  KAKENHI-PROJECT-19K07762
[Presentation] O-GlcNAcylation-mediated degradation of FBXL2 stabilizes FOXM1 oncogenic transcription factor to promote cancer progression.2020
- Author(s)
  K Moriwaki, Y Ueda, K Higuchi, and M Asahi.
- Organizer
  第93回日本薬理学会
- Data Source
  KAKENHI-PROJECT-19K07762
[Presentation] Elevated O-GlcNAcylation increases FOXM1 protein via suppression of its poly-ubiquitination and subsequent proteasomal degradation.2019
- Author(s)
  Y Ueda, K Moriwaki, N Sugawara, M Fukumoto, S Harada, K Ota, Y Kojima, T Takeuchi, K Higuchi, and M Asahi.
- Organizer
  Digestive Disease Week 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K07762
[Presentation] Elevated O-GlcNAcylation increases FOXM1 via suppression of FBXL2-mediated its poly-ubiquitination.2019
- Author(s)
  Moriwaki K, Higuchi K, Asahi M.
- Organizer
  第78回日本癌学会学術総会
- Data Source
  KAKENHI-PROJECT-17K08678
[Presentation] Elevated O-GlcNAcylation increases FOXM1 protein via suppression of its poly-ubiquitination and subsequent proteasomal degradation.2019
- Author(s)
  Ueda Y, Moriwaki K, Sugawara N, Fukumoto M, Harada S, Ota K, Kojima Y, Takeuchi T, Higuchi K, Asahi M.
- Organizer
  Digestive Disease Week
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K08678
[Presentation] O-GlcNAcylation-mediated degradation of FBXL2 stabilizes FOXM1 oncogenic transcription factor to promote cancer progression.2019
- Author(s)
  Moriwaki K, Ueda Y, Higuchi K, Asahi M.
- Organizer
  第93回日本薬理学会年
- Data Source
  KAKENHI-PROJECT-17K08678
[Presentation] Elevated O-GlcNAcylation increases FOXM1 via suppression of FBXL2-mediated its poly-ubiquitination.2019
- Author(s)
  K Moriwaki, K Higuchi, and M Asahi.
- Organizer
  第78回日本癌学会学術総会
- Data Source
  KAKENHI-PROJECT-19K07762

1. 朝日通雄 (10397614)

# of Collaborated Projects: 2 results

# of Collaborated Products: 6 results
2. HIRASHIMA Masanori (40383757)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. DING Guo (00514697)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 竹内利寿 (30445986)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
5. HIGUCHI Kazuhide

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. Inoue Takuya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. Nakagawa Takatoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Moriwaki Kazumasa 森脇 一将

MORIWAKI Kazumasa 森脇 一将

Research Projects

Research Products

Co-Researchers

O-GlcNAc修飾による癌微小環境制御機能の解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of novel diagnosis and therapy in cancer targetting reversible system of intracellular glycosylation

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Role of TME O-GlcNAcylation in cancer proliferationPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Pathology and molecular mechanism of embryonic edema in mice carrying endothelial gene mutations

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] O-GlcNAcylation-mediated degradation of FBXL2 stabilizes FOXM1 to induce cancer progression.2020

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Augmented <i>O</i>-GlcNAcylation alleviates inflammation-mediated colon carcinogenesis via suppression of acute inflammation2018

Author(s)

Journal Title

DOI

NAID

ISSN

Language

Data Source

[Journal Article] Augmented O-GlcNAcylation of AMP-activated kinase promotes the proliferation of LoVo cells, a colon cancer cell line2017

Author(s)

Journal Title

DOI

Data Source

[Presentation] O-GlcNAcylation-mediated regulation of FOXM1 expression through its ubiquitination in a human gastric adenocarcinoma cell line, NUGC-3.2021

Author(s)

Organizer

Data Source

[Presentation] O-GlcNAcylation-mediated degradation of FBXL2 stabilizes FOXM1 oncogenic transcription factor to promote cancer progression.2020

Author(s)

Organizer

Data Source

[Presentation] Elevated O-GlcNAcylation increases FOXM1 protein via suppression of its poly-ubiquitination and subsequent proteasomal degradation.2019

Author(s)

Organizer

Data Source

[Presentation] Elevated O-GlcNAcylation increases FOXM1 via suppression of FBXL2-mediated its poly-ubiquitination.2019

Author(s)

Organizer

Data Source

[Presentation] Elevated O-GlcNAcylation increases FOXM1 protein via suppression of its poly-ubiquitination and subsequent proteasomal degradation.2019

Author(s)

Organizer

Data Source

[Presentation] O-GlcNAcylation-mediated degradation of FBXL2 stabilizes FOXM1 oncogenic transcription factor to promote cancer progression.2019

Author(s)

Organizer

Data Source

[Presentation] Elevated O-GlcNAcylation increases FOXM1 via suppression of FBXL2-mediated its poly-ubiquitination.2019

Author(s)

Organizer

Data Source

Moriwaki Kazumasa 森脇一将

MORIWAKI Kazumasa 森脇一将