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Small molecule activator of Nm23/NDPK as an inhibitor of metastasis
Nm23-H1/NDPK-A is a tumor metastasis suppressor having NDP kinase (NDPK) activity. Nm23-H1 is positively associated with prolonged disease-free survival and good prognosis of cancer patients. Approaches to increasing the cellular levels of Nm23-H1 therefore have significance in the therapy of metast...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053448/ https://www.ncbi.nlm.nih.gov/pubmed/30026594 http://dx.doi.org/10.1038/s41598-018-29101-6 |
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author | Lee, Jae-Jin Kim, Hwang Suk Lee, Ji-Sun Park, Jimin Shin, Sang Chul Song, Soonwha Lee, Eunsun Choi, Jung-Eun Suh, Ji-Wan Lee, Hongsoo Kim, Eunice EunKyeong Seo, Eun Kyoung Shin, Dong Hae Lee, Ho-Young Lee, Hee-Yoon Lee, Kong-Joo |
author_facet | Lee, Jae-Jin Kim, Hwang Suk Lee, Ji-Sun Park, Jimin Shin, Sang Chul Song, Soonwha Lee, Eunsun Choi, Jung-Eun Suh, Ji-Wan Lee, Hongsoo Kim, Eunice EunKyeong Seo, Eun Kyoung Shin, Dong Hae Lee, Ho-Young Lee, Hee-Yoon Lee, Kong-Joo |
author_sort | Lee, Jae-Jin |
collection | PubMed |
description | Nm23-H1/NDPK-A is a tumor metastasis suppressor having NDP kinase (NDPK) activity. Nm23-H1 is positively associated with prolonged disease-free survival and good prognosis of cancer patients. Approaches to increasing the cellular levels of Nm23-H1 therefore have significance in the therapy of metastatic cancers. We found a small molecule, (±)-trans-3-(3,4-dimethoxyphenyl)-4-[(E)-3,4-dimethoxystyryl]cyclohex-1-ene, that activates Nm23, hereafter called NMac1. NMac1 directly binds to Nm23-H1 and increases its NDPK activity. Employing various NMac1 derivatives and hydrogen/deuterium mass spectrometry (HDX-MS), we identified the pharmacophore and mode of action of NMac1. We found that NMac1 binds to the C-terminal of Nm23-H1 and induces the NDPK activation through its allosteric conformational changes. NMac1-treated MDA-MB-231 breast cancer cells showed dramatic changes in morphology and actin-cytoskeletal organization following inhibition of Rac1 activation. NMac1 also suppressed invasion and migration in vitro, and metastasis in vivo, in a breast cancer mouse model. NMac1 as an activator of NDPK has potential as an anti-metastatic agent. |
format | Online Article Text |
id | pubmed-6053448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60534482018-07-23 Small molecule activator of Nm23/NDPK as an inhibitor of metastasis Lee, Jae-Jin Kim, Hwang Suk Lee, Ji-Sun Park, Jimin Shin, Sang Chul Song, Soonwha Lee, Eunsun Choi, Jung-Eun Suh, Ji-Wan Lee, Hongsoo Kim, Eunice EunKyeong Seo, Eun Kyoung Shin, Dong Hae Lee, Ho-Young Lee, Hee-Yoon Lee, Kong-Joo Sci Rep Article Nm23-H1/NDPK-A is a tumor metastasis suppressor having NDP kinase (NDPK) activity. Nm23-H1 is positively associated with prolonged disease-free survival and good prognosis of cancer patients. Approaches to increasing the cellular levels of Nm23-H1 therefore have significance in the therapy of metastatic cancers. We found a small molecule, (±)-trans-3-(3,4-dimethoxyphenyl)-4-[(E)-3,4-dimethoxystyryl]cyclohex-1-ene, that activates Nm23, hereafter called NMac1. NMac1 directly binds to Nm23-H1 and increases its NDPK activity. Employing various NMac1 derivatives and hydrogen/deuterium mass spectrometry (HDX-MS), we identified the pharmacophore and mode of action of NMac1. We found that NMac1 binds to the C-terminal of Nm23-H1 and induces the NDPK activation through its allosteric conformational changes. NMac1-treated MDA-MB-231 breast cancer cells showed dramatic changes in morphology and actin-cytoskeletal organization following inhibition of Rac1 activation. NMac1 also suppressed invasion and migration in vitro, and metastasis in vivo, in a breast cancer mouse model. NMac1 as an activator of NDPK has potential as an anti-metastatic agent. Nature Publishing Group UK 2018-07-19 /pmc/articles/PMC6053448/ /pubmed/30026594 http://dx.doi.org/10.1038/s41598-018-29101-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Jae-Jin Kim, Hwang Suk Lee, Ji-Sun Park, Jimin Shin, Sang Chul Song, Soonwha Lee, Eunsun Choi, Jung-Eun Suh, Ji-Wan Lee, Hongsoo Kim, Eunice EunKyeong Seo, Eun Kyoung Shin, Dong Hae Lee, Ho-Young Lee, Hee-Yoon Lee, Kong-Joo Small molecule activator of Nm23/NDPK as an inhibitor of metastasis |
title | Small molecule activator of Nm23/NDPK as an inhibitor of metastasis |
title_full | Small molecule activator of Nm23/NDPK as an inhibitor of metastasis |
title_fullStr | Small molecule activator of Nm23/NDPK as an inhibitor of metastasis |
title_full_unstemmed | Small molecule activator of Nm23/NDPK as an inhibitor of metastasis |
title_short | Small molecule activator of Nm23/NDPK as an inhibitor of metastasis |
title_sort | small molecule activator of nm23/ndpk as an inhibitor of metastasis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053448/ https://www.ncbi.nlm.nih.gov/pubmed/30026594 http://dx.doi.org/10.1038/s41598-018-29101-6 |
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