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...
Saved in:
Main Authors: | , , , , , , , , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2015
|
Online Access: | https://hdl.handle.net/10356/103986 http://hdl.handle.net/10220/38799 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-103986 |
---|---|
record_format |
dspace |
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 |
_version_ |
1759853244085960704 |