Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock

Sakomoto et al. identify naphthofluorescein as a mint3 inhibitor that disrupts the Mint3–FIH-1 interaction and attenuates HIF-1 activity. In vivo experiments in mice reveal a reduction in tumor growth with attenuated inflammatory cytokine production and endotoxic shock, presenting an option for targ...

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Main Authors: Takeharu Sakamoto, Yuya Fukui, Yasumitsu Kondoh, Kaori Honda, Takeshi Shimizu, Toshiro Hara, Tetsuro Hayashi, Yurika Saitoh, Yoshinori Murakami, Jun-ichiro Inoue, Shuichi Kaneko, Hiroyuki Osada, Motoharu Seiki
Format: Article
Language:English
Published: Nature Publishing Group 2021-10-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-021-02701-1
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spelling doaj-19aa786f0153417ab843292a86a3abc22021-10-10T11:13:13ZengNature Publishing GroupCommunications Biology2399-36422021-10-014111510.1038/s42003-021-02701-1Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shockTakeharu Sakamoto0Yuya Fukui1Yasumitsu Kondoh2Kaori Honda3Takeshi Shimizu4Toshiro Hara5Tetsuro Hayashi6Yurika Saitoh7Yoshinori Murakami8Jun-ichiro Inoue9Shuichi Kaneko10Hiroyuki Osada11Motoharu Seiki12Department of Cancer Biology, Institute of Biomedical Science, Kansai Medical UniversityDepartment of System Biology, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa UniversityChemical Biology Research Group, RIKEN Center for Sustainable Resource ScienceChemical Biology Research Group, RIKEN Center for Sustainable Resource ScienceChemical Biology Research Group, RIKEN Center for Sustainable Resource ScienceDivision of Cancer Cell Research, Institute of Medical Science, The University of TokyoDivision of Molecular Pathology, Institute of Medical Science, The University of TokyoCenter for Medical Education, Teikyo University of ScienceDivision of Molecular Pathology, Institute of Medical Science, The University of TokyoDivision of Cellular and Molecular Biology, The Institute of Medical Science, The University of TokyoDepartment of System Biology, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa UniversityChemical Biology Research Group, RIKEN Center for Sustainable Resource ScienceDivision of Cancer Cell Research, Institute of Medical Science, The University of TokyoSakomoto et al. identify naphthofluorescein as a mint3 inhibitor that disrupts the Mint3–FIH-1 interaction and attenuates HIF-1 activity. In vivo experiments in mice reveal a reduction in tumor growth with attenuated inflammatory cytokine production and endotoxic shock, presenting an option for targeted therapies for cancer and inflammatory diseases that avoid severe adverse effects.https://doi.org/10.1038/s42003-021-02701-1
collection DOAJ
language English
format Article
sources DOAJ
author Takeharu Sakamoto
Yuya Fukui
Yasumitsu Kondoh
Kaori Honda
Takeshi Shimizu
Toshiro Hara
Tetsuro Hayashi
Yurika Saitoh
Yoshinori Murakami
Jun-ichiro Inoue
Shuichi Kaneko
Hiroyuki Osada
Motoharu Seiki
spellingShingle Takeharu Sakamoto
Yuya Fukui
Yasumitsu Kondoh
Kaori Honda
Takeshi Shimizu
Toshiro Hara
Tetsuro Hayashi
Yurika Saitoh
Yoshinori Murakami
Jun-ichiro Inoue
Shuichi Kaneko
Hiroyuki Osada
Motoharu Seiki
Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock
Communications Biology
author_facet Takeharu Sakamoto
Yuya Fukui
Yasumitsu Kondoh
Kaori Honda
Takeshi Shimizu
Toshiro Hara
Tetsuro Hayashi
Yurika Saitoh
Yoshinori Murakami
Jun-ichiro Inoue
Shuichi Kaneko
Hiroyuki Osada
Motoharu Seiki
author_sort Takeharu Sakamoto
title Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock
title_short Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock
title_full Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock
title_fullStr Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock
title_full_unstemmed Pharmacological inhibition of Mint3 attenuates tumour growth, metastasis, and endotoxic shock
title_sort pharmacological inhibition of mint3 attenuates tumour growth, metastasis, and endotoxic shock
publisher Nature Publishing Group
series Communications Biology
issn 2399-3642
publishDate 2021-10-01
description Sakomoto et al. identify naphthofluorescein as a mint3 inhibitor that disrupts the Mint3–FIH-1 interaction and attenuates HIF-1 activity. In vivo experiments in mice reveal a reduction in tumor growth with attenuated inflammatory cytokine production and endotoxic shock, presenting an option for targeted therapies for cancer and inflammatory diseases that avoid severe adverse effects.
url https://doi.org/10.1038/s42003-021-02701-1
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