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Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells
Objectives: Calotropin (CTP), a natural product isolated from Calotropis gigantea, has been identified as a potential anticancer agent. In this study, we aimed to investigate the effect CTP on colorectal cancer and the role of Yes-associated protein (YAP) in CTP-inhibited cell proliferation. Methods...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536122/ https://www.ncbi.nlm.nih.gov/pubmed/31190898 http://dx.doi.org/10.2147/OTT.S200873 |
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author | Zhou, Limin Cai, Luliang Guo, Yanzi Zhang, Huanyu Wang, Peng Yi, Guohui Huang, Yonghao |
author_facet | Zhou, Limin Cai, Luliang Guo, Yanzi Zhang, Huanyu Wang, Peng Yi, Guohui Huang, Yonghao |
author_sort | Zhou, Limin |
collection | PubMed |
description | Objectives: Calotropin (CTP), a natural product isolated from Calotropis gigantea, has been identified as a potential anticancer agent. In this study, we aimed to investigate the effect CTP on colorectal cancer and the role of Yes-associated protein (YAP) in CTP-inhibited cell proliferation. Methods: Cell viability and cell proliferation were detected by MTT and BrdU assay. Western blotting and immunofluorescence were performed to determine CTP-induced YAP dephosphorylation and nuclear localization. Western blotting, siRNA transfection and RT-PCR analysis were carried out to investigate the mechanisms of CTP-mediated YAP activation. The anti-tumor activities of CTP were observed in mice tumor models. Results: We demonstrated that CTP inhibits the proliferation of colorectal cancer cells both in vitro and in vivo. Moreover, we showed that CTP activates YAP in colorectal cancer cells. Mechanistically, CTP promotes LATS1 degradation via the ubiquitination/proteasome pathway, resulting in YAP dephosphorylation and nuclear localization, leading to induce YAP target genes expression in colorectal cancer cells. Inhibition of YAP activity enhances CTP-mediated inhibition of cell proliferation, suggesting that YAP plays a protective role in CTP-induced antiproliferative effect. Conclusion: Our results demonstrate that CTP markedly inhibits tumor growth and activates a protective role of YAP in colorectal cancer cells, indicating that combination of CTP and YAP targeting drugs may be a promising strategy for colorectal cancer treatment. |
format | Online Article Text |
id | pubmed-6536122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-65361222019-06-12 Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells Zhou, Limin Cai, Luliang Guo, Yanzi Zhang, Huanyu Wang, Peng Yi, Guohui Huang, Yonghao Onco Targets Ther Original Research Objectives: Calotropin (CTP), a natural product isolated from Calotropis gigantea, has been identified as a potential anticancer agent. In this study, we aimed to investigate the effect CTP on colorectal cancer and the role of Yes-associated protein (YAP) in CTP-inhibited cell proliferation. Methods: Cell viability and cell proliferation were detected by MTT and BrdU assay. Western blotting and immunofluorescence were performed to determine CTP-induced YAP dephosphorylation and nuclear localization. Western blotting, siRNA transfection and RT-PCR analysis were carried out to investigate the mechanisms of CTP-mediated YAP activation. The anti-tumor activities of CTP were observed in mice tumor models. Results: We demonstrated that CTP inhibits the proliferation of colorectal cancer cells both in vitro and in vivo. Moreover, we showed that CTP activates YAP in colorectal cancer cells. Mechanistically, CTP promotes LATS1 degradation via the ubiquitination/proteasome pathway, resulting in YAP dephosphorylation and nuclear localization, leading to induce YAP target genes expression in colorectal cancer cells. Inhibition of YAP activity enhances CTP-mediated inhibition of cell proliferation, suggesting that YAP plays a protective role in CTP-induced antiproliferative effect. Conclusion: Our results demonstrate that CTP markedly inhibits tumor growth and activates a protective role of YAP in colorectal cancer cells, indicating that combination of CTP and YAP targeting drugs may be a promising strategy for colorectal cancer treatment. Dove 2019-05-23 /pmc/articles/PMC6536122/ /pubmed/31190898 http://dx.doi.org/10.2147/OTT.S200873 Text en © 2019 Zhou et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Zhou, Limin Cai, Luliang Guo, Yanzi Zhang, Huanyu Wang, Peng Yi, Guohui Huang, Yonghao Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells |
title | Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells |
title_full | Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells |
title_fullStr | Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells |
title_full_unstemmed | Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells |
title_short | Calotropin activates YAP through downregulation of LATS1 in colorectal cancer cells |
title_sort | calotropin activates yap through downregulation of lats1 in colorectal cancer cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536122/ https://www.ncbi.nlm.nih.gov/pubmed/31190898 http://dx.doi.org/10.2147/OTT.S200873 |
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