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Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3
Curcumol is the major component extracted from root of Rhizoma Curcumae. Recent studies have shown that curcumol exerts therapeutic effects against multiple conditions, particularly cancers. However, the therapeutic role and mechanism of curcumol against cholangiocarcinoma cells are still unclear. I...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870041/ https://www.ncbi.nlm.nih.gov/pubmed/29615928 http://dx.doi.org/10.3389/fphys.2018.00234 |
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author | Zhang, Jinduo Su, Gang Tang, Zengwei Wang, Li Fu, Wenkang Zhao, Sheng Ba, Yongjiang Bai, Bing Yue, Ping Lin, Yanyan Bai, Zhongtian Hu, Jinjing Meng, Wenbo Qiao, Liang Li, Xun Xie, Xiaodong |
author_facet | Zhang, Jinduo Su, Gang Tang, Zengwei Wang, Li Fu, Wenkang Zhao, Sheng Ba, Yongjiang Bai, Bing Yue, Ping Lin, Yanyan Bai, Zhongtian Hu, Jinjing Meng, Wenbo Qiao, Liang Li, Xun Xie, Xiaodong |
author_sort | Zhang, Jinduo |
collection | PubMed |
description | Curcumol is the major component extracted from root of Rhizoma Curcumae. Recent studies have shown that curcumol exerts therapeutic effects against multiple conditions, particularly cancers. However, the therapeutic role and mechanism of curcumol against cholangiocarcinoma cells are still unclear. In our current research, we tested the effect of curcumol in cholangiocarcinoma cells, and using two-dimensional electrophoresis, proteomics and bioinformatics, we identified cyclin-dependent kinase like 3 (CDKL3) as a potential target for curcumol. We have demonstrated that curcumol can evidently suppress growth and migration of cholangiocarcinoma cells. Furthermore, curcumol could significantly block the cell cycle progression of the cholangiocarcinoma cells. These effects could be largely attributed to the inhibition of CDKL3 by curcumol. Further studies have recapitulated the oncogenic role of CDKL3 in that knockdown of CDKL3 by lentiviral mediated transfection of shRNA against CDKL3 also led to a significant inhibition on cell proliferation, migration, invasion, and cell cycle progression. Given the high level of CDKL3 expression in human cholangiocarcinoma tissues and cell lines, we speculated that CDKL3 may constitute a potential biological target for curcumol in cholangiocarcinoma. |
format | Online Article Text |
id | pubmed-5870041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58700412018-04-03 Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 Zhang, Jinduo Su, Gang Tang, Zengwei Wang, Li Fu, Wenkang Zhao, Sheng Ba, Yongjiang Bai, Bing Yue, Ping Lin, Yanyan Bai, Zhongtian Hu, Jinjing Meng, Wenbo Qiao, Liang Li, Xun Xie, Xiaodong Front Physiol Physiology Curcumol is the major component extracted from root of Rhizoma Curcumae. Recent studies have shown that curcumol exerts therapeutic effects against multiple conditions, particularly cancers. However, the therapeutic role and mechanism of curcumol against cholangiocarcinoma cells are still unclear. In our current research, we tested the effect of curcumol in cholangiocarcinoma cells, and using two-dimensional electrophoresis, proteomics and bioinformatics, we identified cyclin-dependent kinase like 3 (CDKL3) as a potential target for curcumol. We have demonstrated that curcumol can evidently suppress growth and migration of cholangiocarcinoma cells. Furthermore, curcumol could significantly block the cell cycle progression of the cholangiocarcinoma cells. These effects could be largely attributed to the inhibition of CDKL3 by curcumol. Further studies have recapitulated the oncogenic role of CDKL3 in that knockdown of CDKL3 by lentiviral mediated transfection of shRNA against CDKL3 also led to a significant inhibition on cell proliferation, migration, invasion, and cell cycle progression. Given the high level of CDKL3 expression in human cholangiocarcinoma tissues and cell lines, we speculated that CDKL3 may constitute a potential biological target for curcumol in cholangiocarcinoma. Frontiers Media S.A. 2018-03-20 /pmc/articles/PMC5870041/ /pubmed/29615928 http://dx.doi.org/10.3389/fphys.2018.00234 Text en Copyright © 2018 Zhang, Su, Tang, Wang, Fu, Zhao, Ba, Bai, Yue, Lin, Bai, Hu, Meng, Qiao, Li and Xie. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Zhang, Jinduo Su, Gang Tang, Zengwei Wang, Li Fu, Wenkang Zhao, Sheng Ba, Yongjiang Bai, Bing Yue, Ping Lin, Yanyan Bai, Zhongtian Hu, Jinjing Meng, Wenbo Qiao, Liang Li, Xun Xie, Xiaodong Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 |
title | Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 |
title_full | Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 |
title_fullStr | Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 |
title_full_unstemmed | Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 |
title_short | Curcumol Exerts Anticancer Effect in Cholangiocarcinoma Cells via Down-Regulating CDKL3 |
title_sort | curcumol exerts anticancer effect in cholangiocarcinoma cells via down-regulating cdkl3 |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870041/ https://www.ncbi.nlm.nih.gov/pubmed/29615928 http://dx.doi.org/10.3389/fphys.2018.00234 |
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