Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells

Many mitotic kinases have been targeted for the development of anti-cancer drugs, and inhibitors of these kinases have been expected to perform well for cancer therapy. Efforts focused on selecting good targets and finding specific drugs to target are especially needed, largely due to the increased...

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Main Authors: Kim, Seong-Hoon, Ryu, Hye Guk, Lee, Juhyun, Shin, Joon, Harikishore, Amaravadhi, Jung, Hoe-Youn, Kim, Ye Seul, Lyu, Ha-Na, Oh, Eunji, Baek, Nam-In, Choi, Kwan-Yong, Yoon, Ho Sup, Kim, Kyong-Tai
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2015
Online Access:https://hdl.handle.net/10356/103986
http://hdl.handle.net/10220/38799
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1039862023-02-28T17:05:28Z Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells Kim, Seong-Hoon Ryu, Hye Guk Lee, Juhyun Shin, Joon Harikishore, Amaravadhi Jung, Hoe-Youn Kim, Ye Seul Lyu, Ha-Na Oh, Eunji Baek, Nam-In Choi, Kwan-Yong Yoon, Ho Sup Kim, Kyong-Tai School of Biological Sciences Many mitotic kinases have been targeted for the development of anti-cancer drugs, and inhibitors of these kinases have been expected to perform well for cancer therapy. Efforts focused on selecting good targets and finding specific drugs to target are especially needed, largely due to the increased frequency of anti-cancer drugs used in the treatment of lung cancer. Vaccinia-related kinase 1 (VRK1) is a master regulator in lung adenocarcinoma and is considered a key molecule in the adaptive pathway, which mainly controls cell survival. We found that ursolic acid (UA) inhibits the catalytic activity of VRK1 via direct binding to the catalytic domain of VRK1. UA weakens surveillance mechanisms by blocking 53BP1 foci formation induced by VRK1 in lung cancer cells, and possesses synergistic anti-cancer effects with DNA damaging drugs. Taken together, UA can be a good anti-cancer agent for targeted therapy or combination therapy with DNA damaging drugs for lung cancer patients. Published version 2015-10-13T08:37:22Z 2019-12-06T21:23:58Z 2015-10-13T08:37:22Z 2019-12-06T21:23:58Z 2015 2015 Journal Article Kim, S.-H., Ryu, H. G., Lee, J., Shin, J., Harikishore, A., Jung, H.-Y., et al. (2015). Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells. Scientific Reports, 5, 14570-. 2045-2322 https://hdl.handle.net/10356/103986 http://hdl.handle.net/10220/38799 10.1038/srep14570 26412148 en Scientific Reports This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
description Many mitotic kinases have been targeted for the development of anti-cancer drugs, and inhibitors of these kinases have been expected to perform well for cancer therapy. Efforts focused on selecting good targets and finding specific drugs to target are especially needed, largely due to the increased frequency of anti-cancer drugs used in the treatment of lung cancer. Vaccinia-related kinase 1 (VRK1) is a master regulator in lung adenocarcinoma and is considered a key molecule in the adaptive pathway, which mainly controls cell survival. We found that ursolic acid (UA) inhibits the catalytic activity of VRK1 via direct binding to the catalytic domain of VRK1. UA weakens surveillance mechanisms by blocking 53BP1 foci formation induced by VRK1 in lung cancer cells, and possesses synergistic anti-cancer effects with DNA damaging drugs. Taken together, UA can be a good anti-cancer agent for targeted therapy or combination therapy with DNA damaging drugs for lung cancer patients.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Kim, Seong-Hoon
Ryu, Hye Guk
Lee, Juhyun
Shin, Joon
Harikishore, Amaravadhi
Jung, Hoe-Youn
Kim, Ye Seul
Lyu, Ha-Na
Oh, Eunji
Baek, Nam-In
Choi, Kwan-Yong
Yoon, Ho Sup
Kim, Kyong-Tai
format Article
author Kim, Seong-Hoon
Ryu, Hye Guk
Lee, Juhyun
Shin, Joon
Harikishore, Amaravadhi
Jung, Hoe-Youn
Kim, Ye Seul
Lyu, Ha-Na
Oh, Eunji
Baek, Nam-In
Choi, Kwan-Yong
Yoon, Ho Sup
Kim, Kyong-Tai
spellingShingle Kim, Seong-Hoon
Ryu, Hye Guk
Lee, Juhyun
Shin, Joon
Harikishore, Amaravadhi
Jung, Hoe-Youn
Kim, Ye Seul
Lyu, Ha-Na
Oh, Eunji
Baek, Nam-In
Choi, Kwan-Yong
Yoon, Ho Sup
Kim, Kyong-Tai
Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
author_sort Kim, Seong-Hoon
title Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
title_short Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
title_full Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
title_fullStr Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
title_full_unstemmed Ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
title_sort ursolic acid exerts anti-cancer activity by suppressing vaccinia-related kinase 1-mediated damage repair in lung cancer cells
publishDate 2015
url https://hdl.handle.net/10356/103986
http://hdl.handle.net/10220/38799
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