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...

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Veröffentlicht in:Scientific reports 2018-07, Vol.8 (1), p.10909-13, Article 10909
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-018-29101-6