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Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells
Resistance of cancer cells to chemotherapy is a significant problem in oncology, and the development of sensitising agents or small-molecules with new mechanisms of action to kill these cells is needed. Autophagy is a cellular process responsible for the turnover of misfolded proteins or damaged org...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076737/ https://www.ncbi.nlm.nih.gov/pubmed/24981420 http://dx.doi.org/10.1038/srep05510 |
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author | Law, Betty Yuen Kwan Chan, Wai Kit Xu, Su Wei Wang, Jing Rong Bai, Li Ping Liu, Liang Wong, Vincent Kam Wai |
author_facet | Law, Betty Yuen Kwan Chan, Wai Kit Xu, Su Wei Wang, Jing Rong Bai, Li Ping Liu, Liang Wong, Vincent Kam Wai |
author_sort | Law, Betty Yuen Kwan |
collection | PubMed |
description | Resistance of cancer cells to chemotherapy is a significant problem in oncology, and the development of sensitising agents or small-molecules with new mechanisms of action to kill these cells is needed. Autophagy is a cellular process responsible for the turnover of misfolded proteins or damaged organelles, and it also recycles nutrients to maintain energy levels for cell survival. In some apoptosis-resistant cancer cells, autophagy can also enhance the efficacy of anti-cancer drugs through autophagy-mediated mechanisms of cell death. Because the modulation of autophagic processes can be therapeutically useful to circumvent chemoresistance and enhance the effects of cancer treatment, the identification of novel autophagic enhancers for use in oncology is highly desirable. Many novel anti-cancer compounds have been isolated from natural products; therefore, we worked to discover natural, anti-cancer small-molecule enhancers of autophagy. Here, we have identified a group of natural alkaloid small-molecules that function as novel autophagic enhancers. These alkaloids, including liensinine, isoliensinine, dauricine and cepharanthine, stimulated AMPK-mTOR dependent induction of autophagy and autophagic cell death in a panel of apoptosis-resistant cells. Taken together, our work provides novel insights into the biological functions, mechanisms and potential therapeutic values of alkaloids for the induction of autophagy. |
format | Online Article Text |
id | pubmed-4076737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40767372014-07-02 Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells Law, Betty Yuen Kwan Chan, Wai Kit Xu, Su Wei Wang, Jing Rong Bai, Li Ping Liu, Liang Wong, Vincent Kam Wai Sci Rep Article Resistance of cancer cells to chemotherapy is a significant problem in oncology, and the development of sensitising agents or small-molecules with new mechanisms of action to kill these cells is needed. Autophagy is a cellular process responsible for the turnover of misfolded proteins or damaged organelles, and it also recycles nutrients to maintain energy levels for cell survival. In some apoptosis-resistant cancer cells, autophagy can also enhance the efficacy of anti-cancer drugs through autophagy-mediated mechanisms of cell death. Because the modulation of autophagic processes can be therapeutically useful to circumvent chemoresistance and enhance the effects of cancer treatment, the identification of novel autophagic enhancers for use in oncology is highly desirable. Many novel anti-cancer compounds have been isolated from natural products; therefore, we worked to discover natural, anti-cancer small-molecule enhancers of autophagy. Here, we have identified a group of natural alkaloid small-molecules that function as novel autophagic enhancers. These alkaloids, including liensinine, isoliensinine, dauricine and cepharanthine, stimulated AMPK-mTOR dependent induction of autophagy and autophagic cell death in a panel of apoptosis-resistant cells. Taken together, our work provides novel insights into the biological functions, mechanisms and potential therapeutic values of alkaloids for the induction of autophagy. Nature Publishing Group 2014-07-01 /pmc/articles/PMC4076737/ /pubmed/24981420 http://dx.doi.org/10.1038/srep05510 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Law, Betty Yuen Kwan Chan, Wai Kit Xu, Su Wei Wang, Jing Rong Bai, Li Ping Liu, Liang Wong, Vincent Kam Wai Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
title | Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
title_full | Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
title_fullStr | Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
title_full_unstemmed | Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
title_short | Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
title_sort | natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076737/ https://www.ncbi.nlm.nih.gov/pubmed/24981420 http://dx.doi.org/10.1038/srep05510 |
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