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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Series: | Communications Biology |
Online Access: | https://doi.org/10.1038/s42003-021-02701-1 |
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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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